Variant report

Variant	nsv902426
Chromosome Location	chr14:105500760-105537476
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1755)
CpG islands
(count:1709)
Chromatin interactive
region (count:112)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1755 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr14:105512086-105512391	HepG2	liver:	n/a	n/a
2	ARID3A	chr14:105505984-105506220	HepG2	liver:	n/a	n/a
3	ARID3A	chr14:105512055-105512331	K562	blood:	n/a	n/a
4	ATF1	chr14:105531689-105532059	K562	blood:	n/a	n/a
5	ATF2	chr14:105535036-105535648	GM12878	blood:	n/a	n/a
6	ATF2	chr14:105532672-105533249	GM12878	blood:	n/a	n/a
7	ATF2	chr14:105535270-105535705	GM12878	blood:	n/a	n/a
8	ATF2	chr14:105512023-105512788	GM12878	blood:	n/a	n/a
9	ATF2	chr14:105527799-105528595	GM12878	blood:	n/a	n/a
10	ATF2	chr14:105512072-105512529	H1-hESC	embryonic stem cell:	n/a	n/a
11	ATF2	chr14:105531494-105532230	GM12878	blood:	n/a	n/a
12	ATF2	chr14:105512062-105512430	GM12878	blood:	n/a	n/a
13	ATF2	chr14:105533584-105533931	GM12878	blood:	n/a	n/a
14	ATF2	chr14:105536073-105537473	GM12878	blood:	n/a	n/a
15	ATF2	chr14:105512921-105514807	GM12878	blood:	n/a	n/a
16	ATF2	chr14:105527777-105528339	GM12878	blood:	n/a	n/a
17	ATF2	chr14:105532781-105533205	GM12878	blood:	n/a	n/a
18	ATF2	chr14:105529889-105530248	GM12878	blood:	n/a	n/a
19	ATF2	chr14:105531529-105532220	GM12878	blood:	n/a	n/a
20	ATF2	chr14:105533544-105534046	GM12878	blood:	n/a	n/a
21	ATF2	chr14:105514092-105514416	GM12878	blood:	n/a	n/a
22	ATF2	chr14:105531034-105531469	GM12878	blood:	n/a	n/a
23	ATF2	chr14:105536061-105537450	GM12878	blood:	n/a	n/a
24	ATF3	chr14:105511938-105512481	A549	lung:	n/a	chr14:105512234-105512242
25	ATF3	chr14:105531135-105531272	K562	blood:	n/a	chr14:105531137-105531146 chr14:105531208-105531217
26	ATF3	chr14:105512057-105512333	HepG2	liver:	n/a	chr14:105512234-105512242
27	ATF3	chr14:105511986-105512491	A549	lung:	n/a	chr14:105512234-105512242
28	BACH1	chr14:105511954-105512390	H1-hESC	embryonic stem cell:	n/a	n/a
29	BACH1	chr14:105522282-105522707	H1-hESC	embryonic stem cell:	n/a	n/a
30	BACH1	chr14:105512083-105512370	K562	blood:	n/a	n/a
31	BATF	chr14:105514029-105514517	GM12878	blood:	n/a	n/a
32	BATF	chr14:105531625-105532007	GM12878	blood:	n/a	n/a
33	BATF	chr14:105536132-105536977	GM12878	blood:	n/a	n/a
34	BATF	chr14:105535194-105535500	GM12878	blood:	n/a	n/a
35	BATF	chr14:105536272-105536860	GM12878	blood:	n/a	n/a
36	BATF	chr14:105527999-105528412	GM12878	blood:	n/a	n/a
37	BATF	chr14:105537151-105537484	GM12878	blood:	n/a	n/a
38	BATF	chr14:105533606-105533956	GM12878	blood:	n/a	n/a
39	BATF	chr14:105533597-105533966	GM12878	blood:	n/a	n/a
40	BCL11A	chr14:105532774-105533118	GM12878	blood:	n/a	chr14:105532994-105533003
41	BCL11A	chr14:105537096-105537427	GM12878	blood:	n/a	n/a
42	BCL11A	chr14:105531576-105531988	GM12878	blood:	n/a	n/a
43	BCL11A	chr14:105531576-105532060	GM12878	blood:	n/a	n/a
44	BCL11A	chr14:105536105-105536823	GM12878	blood:	n/a	chr14:105536582-105536591 chr14:105536581-105536590 chr14:105536343-105536352
45	BCL11A	chr14:105531169-105531404	GM12878	blood:	n/a	n/a
46	BCL11A	chr14:105533622-105533966	GM12878	blood:	n/a	chr14:105533866-105533874
47	BCL11A	chr14:105536100-105536935	GM12878	blood:	n/a	chr14:105536582-105536591 chr14:105536581-105536590 chr14:105536343-105536352
48	BCL3	chr14:105532742-105533181	GM12878	blood:	n/a	chr14:105532994-105533003
49	BCL3	chr14:105536131-105536912	GM12878	blood:	n/a	chr14:105536582-105536591 chr14:105536581-105536590 chr14:105536343-105536352
50	BCL3	chr14:105511961-105512390	GM12878	blood:	n/a	chr14:105512255-105512268 chr14:105512098-105512111

(count:1709 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:105531855-105531905	Caco-2	colon:	n/a
2	chr14:105531855-105531905	Caco-2	colon:	n/a
3	chr14:105531855-105531905	NB4	blood:	n/a
4	chr14:105512268-105512318	HAEpiC	amniotic membrane:	n/a
5	chr14:105512306-105512356	Hela-S3	cervix:	n/a
6	chr14:105522902-105522952	U87	brain:	n/a
7	chr14:105511982-105512032	NB4	blood:	n/a
8	chr14:105532252-105532302	NB4	blood:	n/a
9	chr14:105532012-105532062	SKMC	muscle:	n/a
10	chr14:105501086-105501136	IMR90	lung:	fetal
11	chr14:105501086-105501136	HRCEpiC	kidney:	n/a
12	chr14:105511982-105512032	GM06990	blood:	n/a
13	chr14:105521842-105521892	ovcar-3	ovarian:	n/a
14	chr14:105521961-105522011	HCT-116	colon:	n/a
15	chr14:105531855-105531905	HEK293	kidney:	embryo
16	chr14:105532252-105532302	CMK	blood:	n/a
17	chr14:105512268-105512318	HCF	heart:	n/a
18	chr14:105532159-105532209	HL-60	blood:	n/a
19	chr14:105518248-105518298	GM12891	blood:	n/a
20	chr14:105521961-105522011	SK-N-SH	brain:	n/a
21	chr14:105531855-105531905	SK-N-SH_RA	brain:	n/a
22	chr14:105517573-105517623	Hepatocyte	liver:	n/a
23	chr14:105521894-105521944	NH-A	brain:	n/a
24	chr14:105532252-105532302	MCF-7	breast:	n/a
25	chr14:105519407-105519457	SK-N-SH	brain:	n/a
26	chr14:105511982-105512032	HCF	heart:	n/a
27	chr14:105532208-105532258	HCPEpiC	choroid plexus:	n/a
28	chr14:105522684-105522734	K562	blood:	n/a
29	chr14:105521894-105521944	GM19239	blood:	n/a
30	chr14:105532159-105532209	ovcar-3	ovarian:	n/a
31	chr14:105522684-105522734	AG10803	skin:	n/a
32	chr14:105501086-105501136	Caco-2	colon:	n/a
33	chr14:105503903-105503953	NB4	blood:	n/a
34	chr14:105517946-105517996	MCF10A-Er-Src	breast:	n/a
35	chr14:105509376-105509426	NHDF-neo	bronchial:	n/a
36	chr14:105532159-105532209	HMEC	breast:	n/a
37	chr14:105512213-105512263	Hepatocyte	liver:	n/a
38	chr14:105522684-105522734	HCPEpiC	choroid plexus:	n/a
39	chr14:105531893-105531943	ovcar-3	ovarian:	n/a
40	chr14:105517946-105517996	HepG2	liver:	n/a
41	chr14:105512306-105512356	Caco-2	colon:	n/a
42	chr14:105522902-105522952	T-47D	breast:	n/a
43	chr14:105509229-105509279	GM12892	blood:	n/a
44	chr14:105512213-105512263	SAEC	small airway:	n/a
45	chr14:105531855-105531905	Hepatocyte	liver:	n/a
46	chr14:105522902-105522952	AG09309	skin:	n/a
47	chr14:105531855-105531905	ECC-1	luminal epithelium:	n/a
48	chr14:105519407-105519457	HAEpiC	amniotic membrane:	n/a
49	chr14:105522348-105522398	AG04450	lung:	fetal
50	chr14:105509376-105509426	Caco-2	colon:	n/a

(count:112 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr14:105450804..105453157-chr14:105503880..105505958,2	MCF-7	breast:
2	chr14:105521494..105526312-chr14:105528458..105531564,4	MCF-7	breast:
3	chr14:105532364..105534245-chr14:105540275..105543125,2	K562	blood:
4	chr14:105442222..105443029-chr14:105532523..105533452,3	MCF-7	breast:
5	chr14:105485028..105487922-chr14:105510838..105513689,3	K562	blood:
6	chr14:105442535..105443057-chr14:105515099..105515632,2	MCF-7	breast:
7	chr14:105458011..105458613-chr14:105511934..105512703,4	MCF-7	breast:
8	chr14:105443874..105446140-chr14:105509434..105514237,4	MCF-7	breast:
9	chr14:105446908..105449625-chr14:105498780..105501070,3	MCF-7	breast:
10	chr14:105499189..105502656-chr14:105506829..105510545,6	MCF-7	breast:
11	chr14:105508361..105510843-chr14:105512303..105515131,2	MCF-7	breast:
12	chr14:105191553..105192162-chr14:105511732..105512291,2	K562	blood:
13	chr14:105439148..105443551-chr14:105514857..105517898,4	MCF-7	breast:
14	chr14:105478262..105479502-chr14:105511768..105512599,7	MCF-7	breast:
15	chr14:105517135..105519527-chr14:105521682..105523635,3	MCF-7	breast:
16	chr14:105512283..105515187-chr14:105515395..105518440,3	MCF-7	breast:
17	chr14:105457715..105458591-chr14:105511755..105512731,6	MCF-7	breast:
18	chr14:105486628..105487531-chr14:105511852..105512355,2	MCF-7	breast:
19	chr14:105516320..105518452-chr14:105527074..105529358,2	MCF-7	breast:
20	chr14:105447672..105451166-chr14:105499426..105503853,4	MCF-7	breast:
21	chr14:105441103..105445393-chr14:105498956..105502062,4	MCF-7	breast:
22	chr14:105441784..105443131-chr14:105511520..105512722,13	MCF-7	breast:
23	chr14:105480559..105481224-chr14:105511646..105512371,2	MCF-7	breast:
24	chr14:105500093..105502246-chr14:105511409..105512946,2	MCF-7	breast:
25	chr14:105399823..105400369-chr14:105511778..105512655,3	MCF-7	breast:
26	chr14:105451336..105453703-chr14:105499245..105500790,2	MCF-7	breast:
27	chr14:105445145..105447583-chr14:105504457..105506627,3	MCF-7	breast:
28	chr14:105499182..105500777-chr14:105502867..105506043,3	MCF-7	breast:
29	chr14:105519950..105521697-chr14:105523622..105526334,2	MCF-7	breast:
30	chr14:105432138..105440616-chr14:105496781..105503324,15	MCF-7	breast:
31	chr14:105441584..105444154-chr14:105510721..105515062,5	K562	blood:
32	chr14:105526612..105528156-chr14:105531987..105533882,2	MCF-7	breast:
33	chr14:105438818..105439783-chr14:105511772..105512631,2	K562	blood:
34	chr14:105512283..105515187-chr14:105515395..105518440,3	MCF-7	breast:
35	chr14:105461096..105464805-chr14:105509582..105512379,4	MCF-7	breast:
36	chr14:105440794..105444073-chr14:105510721..105514386,4	K562	blood:
37	chr14:105511795..105512498-chr14:105553098..105553751,3	MCF-7	breast:
38	chr14:105515500..105519468-chr14:105521561..105526194,6	K562	blood:
39	chr14:105406835..105407618-chr14:105511905..105512554,2	MCF-7	breast:
40	chr14:105452423..105455190-chr14:105511602..105513790,3	MCF-7	breast:
41	chr14:105522574..105524801-chr14:105525749..105528494,2	K562	blood:
42	chr14:105437778..105440413-chr14:105535668..105537696,2	MCF-7	breast:
43	chr14:105512170..105512763-chr14:105653793..105654556,2	MCF-7	breast:
44	chr14:105399296..105399819-chr14:105511246..105512107,2	MCF-7	breast:
45	chr14:105511484..105514787-chr14:105515650..105518482,3	MCF-7	breast:
46	chr14:105362756..105363700-chr14:105511815..105512636,5	K562	blood:
47	chr14:105438710..105440414-chr14:105510653..105512208,2	MCF-7	breast:
48	chr14:105503195..105506061-chr14:105506902..105508657,2	MCF-7	breast:
49	chr14:105432444..105435171-chr14:105511281..105513551,2	MCF-7	breast:
50	chr14:105445779..105447281-chr14:105498227..105500995,2	MCF-7	breast:

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GPR132-1	chr14:105532071-105532089	XLOC_011152
2	lnc-GPR132-1	chr14:105533801-105534066	XLOC_011152
3	lnc-GPR132-2	chr14:105506822-105506849	XLOC_011151
4	lnc-GPR132-2	chr14:105509257-105509821	XLOC_011151
5	lnc-GPR132-1	chr14:105536959-105537000	XLOC_011152

No data

Variant related genes	Relation type
GPR132	TF binding region
GPR132	CpG island
ENSG00000183484	chromatin interactions
ENSG00000136856	chromatin interactions
ENSG00000140104	chromatin interactions
ENSG00000257622	chromatin interactions
ENSG00000170779	chromatin interactions
ENSG00000185567	chromatin interactions
ENSG00000099814	chromatin interactions
ENSG00000183828	chromatin interactions
NASP	miRNA target sites
NARG2	miRNA target sites

Extended variants
information (count: 1491 )
Associated
traits (count: 108 )

Variant overlapped rSNPs/rCNVs (count:1491 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10150848	chr14:105500760-105500761	Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs150232683	chr14:105500771-105500772	Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
3	rs528757264	chr14:105500809-105500810	Enhancers Bivalent Enhancer Weak transcription Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
4	rs573015256	chr14:105500814-105500815	Enhancers Bivalent Enhancer Weak transcription Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
5	rs575246962	chr14:105500816-105500817	Enhancers Bivalent Enhancer Weak transcription Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
6	rs373530640	chr14:105500823-105500824	Enhancers Bivalent Enhancer Weak transcription Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
7	rs116137911	chr14:105500862-105500863	Enhancers Bivalent Enhancer Weak transcription Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
8	rs28539478	chr14:105500883-105500884	Enhancers Bivalent Enhancer Weak transcription Active TSS	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs577211248	chr14:105500895-105500896	Enhancers Bivalent Enhancer Weak transcription Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
10	rs557159856	chr14:105500985-105500986	Enhancers Bivalent Enhancer Weak transcription Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
11	rs567680142	chr14:105501037-105501038	Enhancers Weak transcription Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
12	rs540207235	chr14:105501044-105501045	Enhancers Weak transcription Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
13	rs376181307	chr14:105501054-105501055	Enhancers Weak transcription Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
14	rs546476771	chr14:105501070-105501071	Enhancers Weak transcription Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
15	rs563175186	chr14:105501072-105501073	Enhancers Weak transcription Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
16	rs531910969	chr14:105501075-105501076	Enhancers Weak transcription Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
17	rs377212896	chr14:105501165-105501166	Enhancers Weak transcription Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
18	rs10139093	chr14:105501197-105501198	Enhancers Weak transcription Active TSS	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs372963355	chr14:105501212-105501213	Weak transcription Enhancers Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs377304077	chr14:105501223-105501224	Weak transcription Enhancers Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs542456701	chr14:105501296-105501297	Weak transcription Enhancers Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs572803872	chr14:105501316-105501317	Weak transcription Enhancers Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs184432315	chr14:105501335-105501336	Weak transcription Enhancers Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs558369215	chr14:105501351-105501352	Weak transcription Enhancers Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs575328741	chr14:105501362-105501363	Weak transcription Enhancers Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs544320264	chr14:105501383-105501384	Weak transcription Enhancers Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs189923698	chr14:105501425-105501426	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs562341918	chr14:105501463-105501464	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs557982699	chr14:105501464-105501465	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs369671735	chr14:105501469-105501470	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs117115075	chr14:105501542-105501543	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs529757893	chr14:105501583-105501584	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs7143587	chr14:105501635-105501636	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs560145538	chr14:105501639-105501640	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs527374464	chr14:105501681-105501682	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs182561159	chr14:105501726-105501727	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs552095227	chr14:105501794-105501795	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs369385823	chr14:105501818-105501819	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs35508196	chr14:105501819-105501820	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs571845858	chr14:105501904-105501905	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs530991679	chr14:105501968-105501969	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs551126332	chr14:105502131-105502132	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs567670703	chr14:105502151-105502152	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs60541549	chr14:105502271-105502272	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs187193228	chr14:105502275-105502276	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs143769468	chr14:105502294-105502295	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs190476284	chr14:105502365-105502366	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs117586705	chr14:105502439-105502440	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs180930599	chr14:105502468-105502469	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs544089108	chr14:105502496-105502497	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:108)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
High-proliferative meningiomas	17937814	CNVD
Non-small cell lung cancer	21044232	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Melanoma	18172304	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Medulloblastoma	21979893	CNVD
Oral cancer	21386901	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Hepatocellular carcinoma	22174799	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	CNVD
Breast cancer	17899364	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Renal cell carcinoma	21668985	CNVD
Chronic myeloid leukemia	20724749	CNVD
Wilms tumour	21544195	CNVD
Lung cancer	18438408	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Colorectal cancer	16774939	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Neuroblastoma	18923191	CNVD
Barrett''s syndrome	19417022	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
cataract	16735990	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Developmental delay	21147756	CNVD
Cancer	20164920	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Biliary cancer	19435499	CNVD
Follicular lymphoma	20505157	CNVD
Acute lymphoblastic leukemia	20139093	CNVD
Hepatocellular carcinoma	16750200	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Glioblastoma multiforme	21922591	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Ovarian cancer	22174824	CNVD
Non-small cell lung cancer	18320023	CNVD
Melanoma	17363583	CNVD
Prostate cancer	18632612	CNVD
Congenital heart defect	22367666	CNVD
Developmental delay	22367666	CNVD
Genitourinary abnormalities	22367666	CNVD
Intellectual disability	22367666	CNVD
Microcephaly	22367666	CNVD
Muscularhypotonia	22367666	CNVD
Ocular coloboma	22367666	CNVD
Teratozoospermia	22367666	CNVD
Cervical cancer	21062161	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Breast cancer	21990379	CNVD
Breast cancer	16417655	CNVD
22q11 deletion syndrome	22511897	CNVD
Cancer	21129771	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Schizophrenia	21399695	CNVD
Intracranial ependymoma	16609018	CNVD
Lung adenocarcinoma	17086460	CNVD
Gastric adenocarcinoma	19115996	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
14q deletion syndrome	22511897	CNVD
Epilepsy	22083797	CNVD
Urothelial carcinoma	21177765	CNVD
Ovarian cancer	21720365	CNVD
Cancer	17440070	CNVD
Neurocytoma	17123091	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Central neurocytomas	17123091	CNVD
Acute lymphoblastic leukemia	17315016	CNVD
Lung cancer	17086460	CNVD
Mortal	21835882	CNVD
small cell lung cancer	17426248	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Schizophrenia	20967226	CNVD
early-passage human iPS cells	21368824	CNVD
Williams Syndrome	20824207	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Pancreatic cancer	17952125	CNVD
Schizophrenia	23813976	CNVD
lymphocytic leukemia	21291569	CNVD
Cancer	20164919	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Recurrent pregnancy loss	19789632	CNVD
Multiple sclerosis	20428171	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:1151 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:105497800-105507800	Weak transcription	K562	blood
2	chr14:105499600-105501000	Active TSS	NHEK	skin
3	chr14:105499600-105501400	Active TSS	NH-A	brain
4	chr14:105500000-105500800	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
5	chr14:105500200-105500800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
6	chr14:105500200-105501000	Enhancers	Primary hematopoietic stem cells short term culture	blood
7	chr14:105500400-105500800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
8	chr14:105500400-105500800	Enhancers	Placenta	Placenta
9	chr14:105500400-105501000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
10	chr14:105500400-105501200	Enhancers	Primary monocytes fromperipheralblood	blood
11	chr14:105500400-105503200	Weak transcription	Pancreatic Islets	Pancreatic Islet
12	chr14:105500400-105503800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
13	chr14:105500400-105504200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
14	chr14:105500400-105505800	Weak transcription	A549	lung
15	chr14:105500600-105500800	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
16	chr14:105500600-105500800	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
17	chr14:105500600-105500800	Flanking Bivalent TSS/Enh	iPS-15b Cell Line	embryonic stem cell
18	chr14:105500600-105500800	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
19	chr14:105500600-105500800	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
20	chr14:105500600-105500800	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
21	chr14:105500600-105501000	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
22	chr14:105500600-105501200	Enhancers	ES-I3 Cell Line	embryonic stem cell
23	chr14:105500600-105501200	Weak transcription	Rectal Mucosa Donor 29	rectum
24	chr14:105500600-105508000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
25	chr14:105500600-105512000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
26	chr14:105500800-105501000	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
27	chr14:105500800-105501000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
28	chr14:105500800-105501000	Bivalent Enhancer	Fetal Muscle Leg	muscle
29	chr14:105500800-105501000	Enhancers	Monocytes-CD14+_RO01746	blood
30	chr14:105500800-105507600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
31	chr14:105501000-105501200	Enhancers	Primary T killer memory cells from peripheral blood	blood
32	chr14:105501200-105501400	Enhancers	Rectal Mucosa Donor 29	rectum
33	chr14:105501200-105504600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
34	chr14:105503800-105504000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
35	chr14:105504000-105504600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
36	chr14:105504200-105504400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
37	chr14:105504400-105504800	Enhancers	Fetal Heart	heart
38	chr14:105504400-105507200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
39	chr14:105504600-105504800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
40	chr14:105504600-105505600	Enhancers	ES-I3 Cell Line	embryonic stem cell
41	chr14:105504600-105506000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
42	chr14:105504800-105505800	Weak transcription	Fetal Heart	heart
43	chr14:105504800-105512000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
44	chr14:105505200-105505400	Enhancers	Muscle Satellite Cultured Cells	--
45	chr14:105505200-105505400	Bivalent Enhancer	HepG2	liver
46	chr14:105505200-105506000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr14:105505200-105506000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
48	chr14:105505600-105505800	Enhancers	HepG2	liver
49	chr14:105505800-105506000	Enhancers	Right Ventricle	heart
50	chr14:105505800-105506200	Enhancers	A549	lung

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