Variant report

Variant	nsv904364
Chromosome Location	chr15:74709975-74728149
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1080)
CpG islands
(count:1162)
Chromatin interactive
region (count:67)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1080 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:74715318-74715492	HepG2	liver:	n/a	n/a
2	ARID3A	chr15:74726253-74726286	K562	blood:	n/a	n/a
3	ATF1	chr15:74718102-74718311	K562	blood:	n/a	n/a
4	ATF2	chr15:74722812-74723350	GM12878	blood:	n/a	n/a
5	ATF2	chr15:74720720-74721192	GM12878	blood:	n/a	n/a
6	ATF2	chr15:74722838-74723267	GM12878	blood:	n/a	n/a
7	ATF2	chr15:74725996-74726787	GM12878	blood:	n/a	n/a
8	BACH1	chr15:74715730-74716028	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr15:74725906-74725939	K562	blood:	n/a	n/a
10	BACH1	chr15:74726362-74726672	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr15:74715311-74715511	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chr15:74725857-74726057	H1-hESC	embryonic stem cell:	n/a	n/a
13	BATF	chr15:74726148-74726611	GM12878	blood:	n/a	n/a
14	BCL11A	chr15:74726241-74726662	GM12878	blood:	n/a	chr15:74726471-74726480 chr15:74726372-74726381
15	BCL3	chr15:74726038-74726603	GM12878	blood:	n/a	chr15:74726471-74726480 chr15:74726064-74726077 chr15:74726372-74726381 chr15:74726063-74726076
16	BCLAF1	chr15:74720588-74721799	GM12878	blood:	n/a	chr15:74720893-74720902
17	BCLAF1	chr15:74726006-74726666	GM12878	blood:	n/a	chr15:74726471-74726480 chr15:74726064-74726077 chr15:74726372-74726381 chr15:74726022-74726035 chr15:74726063-74726076
18	BCLAF1	chr15:74725906-74726705	GM12878	blood:	n/a	chr15:74726471-74726480 chr15:74726064-74726077 chr15:74726372-74726381 chr15:74726022-74726035 chr15:74726063-74726076
19	BCLAF1	chr15:74717831-74718350	GM12878	blood:	n/a	n/a
20	BHLHE40	chr15:74715011-74715309	GM12878	blood:	n/a	n/a
21	BHLHE40	chr15:74716460-74716593	K562	blood:	n/a	n/a
22	BHLHE40	chr15:74717998-74718303	K562	blood:	n/a	n/a
23	BHLHE40	chr15:74725856-74726684	K562	blood:	n/a	chr15:74726022-74726038
24	BHLHE40	chr15:74722829-74723197	GM12878	blood:	n/a	n/a
25	BHLHE40	chr15:74725374-74725482	GM12878	blood:	n/a	n/a
26	BHLHE40	chr15:74725918-74726764	GM12878	blood:	n/a	chr15:74726022-74726038
27	BHLHE40	chr15:74725905-74726657	HepG2	liver:	n/a	chr15:74726022-74726038
28	BHLHE40	chr15:74715185-74715213	K562	blood:	n/a	n/a
29	BHLHE40	chr15:74714990-74715773	HepG2	liver:	n/a	chr15:74715008-74715024
30	BRCA1	chr15:74712549-74712574	GM12878	blood:	n/a	n/a
31	BRCA1	chr15:74728070-74728188	GM12878	blood:	n/a	n/a
32	BRCA1	chr15:74716073-74716075	HepG2	liver:	n/a	n/a
33	CBX3	chr15:74717996-74718373	K562	blood:	n/a	n/a
34	CBX3	chr15:74725794-74726155	K562	blood:	n/a	n/a
35	CCNT2	chr15:74724803-74726548	K562	blood:	n/a	chr15:74725140-74725149 chr15:74726366-74726375 chr15:74725787-74725796 chr15:74725056-74725065 chr15:74726361-74726370 chr15:74726373-74726382 chr15:74725169-74725178
36	CCNT2	chr15:74717925-74718315	K562	blood:	n/a	n/a
37	CEBPB	chr15:74715024-74715461	IMR90	lung:	n/a	chr15:74715131-74715148
38	CEBPB	chr15:74719897-74720254	HepG2	liver:	n/a	chr15:74720069-74720080
39	CEBPB	chr15:74719920-74720257	HepG2	liver:	n/a	chr15:74720069-74720080
40	CEBPB	chr15:74715338-74715511	Hela-S3	cervix:	n/a	n/a
41	CEBPB	chr15:74719987-74720199	Hela-S3	cervix:	n/a	chr15:74720069-74720080
42	CEBPB	chr15:74715316-74715323	H1-hESC	embryonic stem cell:	n/a	n/a
43	CEBPB	chr15:74722751-74723767	GM12878	blood:	n/a	n/a
44	CEBPB	chr15:74726217-74726862	GM12878	blood:	n/a	n/a
45	CEBPB	chr15:74718109-74718218	K562	blood:	n/a	n/a
46	CEBPB	chr15:74714996-74715499	HepG2	liver:	n/a	chr15:74715131-74715148
47	CEBPD	chr15:74713862-74714212	HepG2	liver:	n/a	n/a
48	CEBPD	chr15:74726114-74726409	HepG2	liver:	n/a	n/a
49	CEBPD	chr15:74726093-74726573	HepG2	liver:	n/a	n/a
50	CHD1	chr15:74722765-74723617	GM12878	blood:	n/a	n/a

(count:1162 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:74725593-74725643	H1-hESC	embryonic stem cell:	embryo
2	chr15:74725882-74725932	A549	lung:	n/a
3	chr15:74726561-74726611	HCM	heart:	n/a
4	chr15:74725593-74725643	H1-hESC	embryonic stem cell:	embryo
5	chr15:74725882-74725932	A549	lung:	n/a
6	chr15:74726561-74726611	HCM	heart:	n/a
7	chr15:74725593-74725643	HEEpiC	esophagus:	n/a
8	chr15:74726561-74726611	ECC-1	luminal epithelium:	n/a
9	chr15:74725593-74725643	ovcar-3	ovarian:	n/a
10	chr15:74724562-74724612	AoSMC	blood vessel:	n/a
11	chr15:74723271-74723321	HCM	heart:	n/a
12	chr15:74726457-74726507	HRCEpiC	kidney:	n/a
13	chr15:74726520-74726570	GM12892	blood:	n/a
14	chr15:74726423-74726473	H1-hESC	embryonic stem cell:	embryo
15	chr15:74726139-74726189	GM06990	blood:	n/a
16	chr15:74726469-74726519	HCPEpiC	choroid plexus:	n/a
17	chr15:74726614-74726664	AG09309	skin:	n/a
18	chr15:74726520-74726570	AoSMC	blood vessel:	n/a
19	chr15:74726561-74726611	NB4	blood:	n/a
20	chr15:74725662-74725712	IMR90	lung:	fetal
21	chr15:74726423-74726473	SKMC	muscle:	n/a
22	chr15:74714463-74714513	Hepatocyte	liver:	n/a
23	chr15:74726136-74726186	AG09319	gingival:	n/a
24	chr15:74714463-74714513	NB4	blood:	n/a
25	chr15:74723271-74723321	Jurkat	blood:	n/a
26	chr15:74724918-74724968	U87	brain:	n/a
27	chr15:74726614-74726664	SKMC	muscle:	n/a
28	chr15:74723271-74723321	AG09319	gingival:	n/a
29	chr15:74726136-74726186	HCF	heart:	n/a
30	chr15:74726136-74726186	T-47D	breast:	n/a
31	chr15:74714463-74714513	Caco-2	colon:	n/a
32	chr15:74726614-74726664	PFSK-1	brain:	n/a
33	chr15:74725593-74725643	BE2_C	brain:	n/a
34	chr15:74715105-74715155	NB4	blood:	n/a
35	chr15:74714463-74714513	HCT-116	colon:	n/a
36	chr15:74726614-74726664	BJ	skin:	n/a
37	chr15:74726486-74726536	PANC-1	pancreas:	n/a
38	chr15:74726520-74726570	HEK293	kidney:	embryo
39	chr15:74726469-74726519	HRCEpiC	kidney:	n/a
40	chr15:74726520-74726570	CMK	blood:	n/a
41	chr15:74724562-74724612	T-47D	breast:	n/a
42	chr15:74726520-74726570	PANC-1	pancreas:	n/a
43	chr15:74715105-74715155	AG09309	skin:	n/a
44	chr15:74715105-74715155	SK-N-SH_RA	brain:	n/a
45	chr15:74724562-74724612	LNCaP	prostate:	n/a
46	chr15:74726520-74726570	GM19239	blood:	n/a
47	chr15:74726139-74726189	GM12892	blood:	n/a
48	chr15:74725980-74726030	NT2-D1	testis:	n/a
49	chr15:74725882-74725932	PrEC	prostate:	n/a
50	chr15:74726469-74726519	HEEpiC	esophagus:	n/a

(count:67 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr15:74674587..74678748-chr15:74711681..74714409,4	K562	blood:
2	chr15:74715079..74717127-chr15:74720885..74723638,2	MCF-7	breast:
3	chr15:74694166..74696263-chr15:74727466..74729822,2	MCF-7	breast:
4	chr15:74692322..74695920-chr15:74711238..74714934,4	K562	blood:
5	chr15:74680306..74681854-chr15:74712615..74715350,2	MCF-7	breast:
6	chr15:74709821..74711608-chr15:74905554..74908094,2	MCF-7	breast:
7	chr15:74715079..74717127-chr15:74720885..74723638,2	MCF-7	breast:
8	chr15:74703939..74707088-chr15:74707597..74710860,4	K562	blood:
9	chr15:74666968..74670060-chr15:74726920..74730762,3	K562	blood:
10	chr15:74709055..74711069-chr15:74716225..74718265,2	MCF-7	breast:
11	chr15:74681432..74683884-chr15:74728087..74731216,4	K562	blood:
12	chr15:74712461..74714565-chr15:74744762..74746348,2	MCF-7	breast:
13	chr15:74685612..74687526-chr15:74716877..74719383,2	K562	blood:
14	chr15:74675641..74677310-chr15:74711681..74714409,2	K562	blood:
15	chr15:74708765..74710665-chr15:74717275..74720280,3	K562	blood:
16	chr15:74715058..74717919-chr15:74753629..74755415,2	K562	blood:
17	chr15:74673143..74676106-chr15:74720304..74723999,3	K562	blood:
18	chr15:74711559..74715833-chr15:74724252..74727151,6	K562	blood:
19	chr15:74725918..74726573-chr6:157802147..157802863,2	HCT-116	colon:
20	chr15:74720298..74721801-chr15:74727091..74728921,2	MCF-7	breast:
21	chr15:74710597..74712982-chr15:75051460..75053643,2	K562	blood:
22	chr15:74710571..74713498-chr15:74715208..74717540,3	K562	blood:
23	chr15:74675805..74678192-chr15:74715315..74717229,2	MCF-7	breast:
24	chr11:94300330..94300985-chr15:74726326..74726975,2	NB4	blood:
25	chr15:74706547..74708360-chr15:74715336..74717632,2	K562	blood:
26	chr15:74725782..74726755-chr17:41465710..41466295,2	NB4	blood:
27	chr15:74664841..74669022-chr15:74717731..74721779,3	K562	blood:
28	chr15:74693785..74695419-chr15:74712435..74714990,2	MCF-7	breast:
29	chr15:74724666..74727655-chr15:74741238..74745335,3	MCF-7	breast:
30	chr15:74679411..74681539-chr15:74718072..74720189,2	K562	blood:
31	chr12:22777643..22778220-chr15:74725782..74726536,2	NB4	blood:
32	chr15:74712692..74714612-chr15:74714775..74716965,2	MCF-7	breast:
33	chr15:74709055..74711069-chr15:74716225..74718265,2	MCF-7	breast:
34	chr15:74678579..74680979-chr15:74717975..74720152,2	MCF-7	breast:
35	chr15:74727453..74729431-chr15:74732496..74734261,2	K562	blood:
36	chr15:74665724..74666602-chr15:74716103..74717034,2	K562	blood:
37	chr15:74698938..74701316-chr15:74711313..74715118,3	MCF-7	breast:
38	chr15:74665092..74667430-chr15:74726842..74729796,2	K562	blood:
39	chr15:74712692..74714612-chr15:74714775..74716965,2	MCF-7	breast:
40	chr15:74718075..74720590-chr15:74744935..74747887,2	K562	blood:
41	chr15:74711706..74714244-chr15:74719320..74721195,2	K562	blood:
42	chr15:74720298..74721801-chr15:74727091..74728921,2	MCF-7	breast:
43	chr15:74708430..74711665-chr15:74722964..74726115,3	K562	blood:
44	chr15:74706143..74707711-chr15:74709343..74712295,2	K562	blood:
45	chr15:74708765..74710665-chr15:74717275..74720280,3	K562	blood:
46	chr15:74683786..74686291-chr15:74709517..74711848,2	K562	blood:
47	chr15:74708483..74711346-chr15:74713083..74715062,3	MCF-7	breast:
48	chr15:74713352..74715766-chr15:74724000..74726928,3	MCF-7	breast:
49	chr15:74689719..74694435-chr15:74706184..74713253,9	MCF-7	breast:
50	chr15:74724949..74727531-chr15:74752948..74755543,2	K562	blood:

No data

Variant related genes	Relation type
SEMA7A	TF binding region
SEMA7A	CpG island
ENSG00000139163	chromatin interactions
ENSG00000257023	chromatin interactions
ENSG00000138623	chromatin interactions
ENSG00000138629	chromatin interactions
ENSG00000188825	chromatin interactions
ENSG00000175048	chromatin interactions
ENSG00000102221	chromatin interactions
ENSG00000260919	chromatin interactions
ENSG00000179335	chromatin interactions
ENSG00000134627	chromatin interactions
ENSG00000247240	chromatin interactions

Extended variants
information (count: 661 )
Associated
traits (count: 68 )

Variant overlapped rSNPs/rCNVs (count:661 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2075589	chr15:74709975-74709976	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs138109375	chr15:74709989-74709990	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs142309393	chr15:74709990-74709991	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs373950889	chr15:74710001-74710002	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs370457755	chr15:74710051-74710052	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs148587534	chr15:74710056-74710057	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs535164102	chr15:74710122-74710123	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs28362915	chr15:74710125-74710126	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs34432520	chr15:74710126-74710127	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs569326273	chr15:74710149-74710150	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs553530865	chr15:74710153-74710154	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs558015385	chr15:74710158-74710159	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs202174103	chr15:74710170-74710171	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs377593968	chr15:74710171-74710172	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs373889584	chr15:74710198-74710199	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs200895370	chr15:74710241-74710242	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs368613221	chr15:74710242-74710243	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs200205962	chr15:74710245-74710246	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs371343346	chr15:74710304-74710305	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs28362914	chr15:74710305-74710306	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs369139994	chr15:74710325-74710326	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs371820373	chr15:74710343-74710344	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs563510463	chr15:74710345-74710346	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs202218725	chr15:74710357-74710358	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs80104948	chr15:74710385-74710386	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs564371788	chr15:74710415-74710416	Weak transcription Genic enhancers Strong transcription Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs142674027	chr15:74710437-74710438	Weak transcription Genic enhancers Strong transcription Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs546630174	chr15:74710449-74710450	Weak transcription Genic enhancers Strong transcription Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs147349163	chr15:74710464-74710465	Weak transcription Genic enhancers Strong transcription Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs28362913	chr15:74710465-74710466	Weak transcription Genic enhancers Strong transcription Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs2072649	chr15:74710485-74710486	Weak transcription Genic enhancers Strong transcription Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs148414538	chr15:74710491-74710492	Weak transcription Genic enhancers Strong transcription Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs539624313	chr15:74710502-74710503	Weak transcription Genic enhancers Strong transcription Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs551697827	chr15:74710507-74710508	Weak transcription Genic enhancers Strong transcription Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs554489630	chr15:74710514-74710515	Weak transcription Genic enhancers Strong transcription Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs28362912	chr15:74710593-74710594	Weak transcription Genic enhancers Strong transcription Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs201477259	chr15:74710602-74710603	Weak transcription Genic enhancers Strong transcription Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs2577109	chr15:74710603-74710604	Weak transcription Genic enhancers Strong transcription Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs372161007	chr15:74710611-74710612	Weak transcription Genic enhancers Strong transcription Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs200795887	chr15:74710614-74710615	Weak transcription Genic enhancers Strong transcription Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs578217064	chr15:74710635-74710636	Weak transcription Genic enhancers Strong transcription Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs16968733	chr15:74710638-74710639	Weak transcription Genic enhancers Strong transcription Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs540617650	chr15:74710642-74710643	Weak transcription Genic enhancers Strong transcription Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs142553012	chr15:74710681-74710682	Weak transcription Genic enhancers Strong transcription Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs369860547	chr15:74710688-74710689	Weak transcription Genic enhancers Strong transcription Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs373368421	chr15:74710698-74710699	Weak transcription Genic enhancers Strong transcription Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs575440580	chr15:74710755-74710756	Weak transcription Genic enhancers Strong transcription Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs546013630	chr15:74710760-74710761	Weak transcription Genic enhancers Strong transcription Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs564235252	chr15:74710851-74710852	Weak transcription Genic enhancers Enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs28362911	chr15:74710852-74710853	Weak transcription Genic enhancers Enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:68)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Schizophrenia	19415332	CNVD
Breast cancer	22522925	CNVD
Wilms tumour	21544195	CNVD
Testicular germ cell tumor	18059402	CNVD
cataract	16735990	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Medulloblastoma	21979893	CNVD
spastic paraplegia with thinning of corpus callosum	19105190	CNVD
Schizophrenia	21324950	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Disease	21824424	CNVD
Melanoma	18172304	CNVD
Gastric cancer	17167181	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Colorectal cancer	16272173	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Multiple myeloma	17550852	CNVD
Intellectual disability	22102821	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	20729466	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Multiple myeloma	20724749	CNVD
Lung cancer	18438408	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Prostate cancer	18632612	CNVD
small cell lung cancer	20016488	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Cancer	16751803	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Breast cancer	17133270	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Prostate cancer	16573809	CNVD
Autism	17322880	CNVD
phobic disorder	16773131	CNVD
Autism	21480499	CNVD
Disorders of sex development	22290220	CNVD
Mental retardation	19951919	CNVD
Mental retardation	16773131	CNVD
T-cell lymphomas	19863542	CNVD
15q24 microdeletion syndrome	22180641	CNVD
15q24 microdeletion syndrome	19921647	CNVD
Disease	22216833	CNVD
Mental retardation	17360722	CNVD
15q24 microdeletion syndrome	22216833	CNVD
15q24 microdeletion syndrome	22283845	CNVD
Developmental delay	17932688	CNVD
craniofacial dysmorphism	17932688	CNVD
digital and genital abnormalities	17932688	CNVD
Breast cancer	21364760	CNVD
Epilepsy	22083797	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Myelofibrosis	22110671	CNVD
Pancreatic cancer	17952125	CNVD
Bipolar disorder	19114987	CNVD

Chromatin state (count:1298 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:74696200-74710400	Weak transcription	Sigmoid Colon	Sigmoid Colon
2	chr15:74696200-74711400	Weak transcription	Skeletal Muscle Female	skeletal muscle
3	chr15:74696200-74712600	Weak transcription	Right Atrium	heart
4	chr15:74696400-74712200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
5	chr15:74697000-74712400	Weak transcription	Fetal Heart	heart
6	chr15:74697000-74712600	Weak transcription	Fetal Lung	lung
7	chr15:74699600-74716600	Weak transcription	Fetal Kidney	kidney
8	chr15:74700000-74713800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
9	chr15:74700200-74711200	Weak transcription	Fetal Intestine Large	intestine
10	chr15:74700400-74710800	Weak transcription	Ovary	ovary
11	chr15:74700600-74712200	Weak transcription	Fetal Brain Male	brain
12	chr15:74700800-74712400	Weak transcription	Rectal Mucosa Donor 29	rectum
13	chr15:74701200-74714600	Genic enhancers	Spleen	Spleen
14	chr15:74701400-74712600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
15	chr15:74702000-74710800	Strong transcription	Brain Germinal Matrix	brain
16	chr15:74702000-74712400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
17	chr15:74702200-74710800	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
18	chr15:74702200-74710800	Strong transcription	Placenta Amnion	Placenta Amnion
19	chr15:74702200-74715000	Weak transcription	Colonic Mucosa	Colon
20	chr15:74702400-74710400	Strong transcription	HUES6 Cell Line	embryonic stem cell
21	chr15:74702400-74711000	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
22	chr15:74702400-74711200	Strong transcription	Fetal Stomach	stomach
23	chr15:74702600-74710400	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
24	chr15:74702600-74711000	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
25	chr15:74702600-74712200	Strong transcription	NHEK	skin
26	chr15:74702800-74712200	Weak transcription	Pancreas	Pancrea
27	chr15:74703000-74710800	Strong transcription	HepG2	liver
28	chr15:74703200-74712600	Weak transcription	Duodenum Mucosa	Duodenum
29	chr15:74703200-74713000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
30	chr15:74703800-74713000	Weak transcription	Duodenum Smooth Muscle	Duodenum
31	chr15:74704400-74710800	Strong transcription	K562	blood
32	chr15:74704600-74711200	Weak transcription	Liver	Liver
33	chr15:74705200-74712800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
34	chr15:74705400-74710400	Strong transcription	Primary T helper cells PMA-I stimulated	--
35	chr15:74705800-74711200	Strong transcription	Fetal Brain Female	brain
36	chr15:74705800-74711400	Genic enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
37	chr15:74706200-74710600	Strong transcription	Gastric	stomach
38	chr15:74706200-74713600	Transcr. at gene 5' and 3'	Foreskin Fibroblast Primary Cells skin01	Skin
39	chr15:74706400-74711800	Genic enhancers	NH-A	brain
40	chr15:74706400-74714600	Genic enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
41	chr15:74706600-74710400	Strong transcription	H9 Cell Line	embryonic stem cell
42	chr15:74706800-74710400	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
43	chr15:74706800-74710400	Strong transcription	Lung	lung
44	chr15:74706800-74711800	Genic enhancers	Thymus	Thymus
45	chr15:74706800-74715000	Weak transcription	Aorta	Aorta
46	chr15:74707200-74710200	Strong transcription	Foreskin Melanocyte Primary Cells skin01	Skin
47	chr15:74707200-74711400	Genic enhancers	Placenta	Placenta
48	chr15:74707200-74722400	Weak transcription	Fetal Intestine Small	intestine
49	chr15:74707400-74712200	Genic enhancers	GM12878-XiMat	blood
50	chr15:74707600-74710600	Genic enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow

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