Variant report

Variant	esv3424416
Chromosome Location	chr5:177556571-177559319
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:594)
CpG islands
(count:489)
Chromatin interactive
region (count:17)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:594 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:177557739-177558118	K562	blood:	n/a	n/a
2	ARID3A	chr5:177557830-177558062	HepG2	liver:	n/a	n/a
3	ATF2	chr5:177558556-177558860	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF2	chr5:177557430-177558012	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr5:177557605-177558044	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr5:177557758-177558026	K562	blood:	n/a	n/a
7	BCL3	chr5:177557478-177558285	GM12878	blood:	n/a	chr5:177558125-177558138 chr5:177557919-177557932 chr5:177557862-177557875 chr5:177557992-177558001 chr5:177557993-177558006
8	BCLAF1	chr5:177557490-177558269	GM12878	blood:	n/a	chr5:177558125-177558138 chr5:177557919-177557932 chr5:177557862-177557875 chr5:177557992-177558001 chr5:177557993-177558006
9	BHLHE40	chr5:177557536-177558398	K562	blood:	n/a	chr5:177558245-177558261 chr5:177557665-177557681
10	BHLHE40	chr5:177557734-177558111	A549	lung:	n/a	n/a
11	BHLHE40	chr5:177557511-177558416	GM12878	blood:	n/a	chr5:177558245-177558261 chr5:177557665-177557681
12	BHLHE40	chr5:177557546-177558397	HepG2	liver:	n/a	chr5:177558245-177558261 chr5:177557665-177557681
13	BRCA1	chr5:177557782-177558206	HepG2	liver:	n/a	n/a
14	BRCA1	chr5:177557708-177558112	Hela-S3	cervix:	n/a	n/a
15	BRCA1	chr5:177557731-177557987	H1-hESC	embryonic stem cell:	n/a	n/a
16	CBX3	chr5:177557309-177558084	K562	blood:	n/a	n/a
17	CCNT2	chr5:177557481-177558377	K562	blood:	n/a	n/a
18	CEBPB	chr5:177557710-177558002	H1-hESC	embryonic stem cell:	n/a	n/a
19	CEBPB	chr5:177557828-177558183	Hela-S3	cervix:	n/a	n/a
20	CEBPD	chr5:177557513-177558273	HepG2	liver:	n/a	n/a
21	CHD1	chr5:177557357-177558395	H1-hESC	embryonic stem cell:	n/a	n/a
22	CHD1	chr5:177557425-177558495	IMR90	lung:	n/a	n/a
23	CHD1	chr5:177557507-177558395	GM12878	blood:	n/a	n/a
24	CHD2	chr5:177557711-177558393	HepG2	liver:	n/a	n/a
25	CHD2	chr5:177557561-177558357	Hela-S3	cervix:	n/a	n/a
26	CHD2	chr5:177557536-177558241	H1-hESC	embryonic stem cell:	n/a	n/a
27	CHD2	chr5:177557426-177558368	GM12878	blood:	n/a	n/a
28	CHD2	chr5:177557485-177558405	K562	blood:	n/a	n/a
29	CREB1	chr5:177557517-177558235	GM12878	blood:	n/a	n/a
30	CREB1	chr5:177557477-177558262	A549	lung:	n/a	n/a
31	CREB1	chr5:177557456-177558210	H1-hESC	embryonic stem cell:	n/a	n/a
32	CREB1	chr5:177557804-177558112	A549	lung:	n/a	n/a
33	CREB1	chr5:177557525-177558322	HepG2	liver:	n/a	n/a
34	CREB1	chr5:177557486-177558173	H1-hESC	embryonic stem cell:	n/a	n/a
35	CREB1	chr5:177557654-177558149	K562	blood:	n/a	n/a
36	CTCF	chr5:177557520-177557670	A549	lung:	n/a	n/a
37	CTCF	chr5:177557540-177557690	SAEC	small airway:	n/a	n/a
38	CTCF	chr5:177557445-177557521	GM13977	blood:	n/a	n/a
39	CTCF	chr5:177558358-177558459	MCF-7	breast:	n/a	n/a
40	CTCF	chr5:177558385-177558427	GM19238	blood:	n/a	n/a
41	CTCF	chr5:177558401-177558455	MCF-7	breast:	n/a	n/a
42	CTCF	chr5:177557620-177557770	SK-N-SH_RA	brain:	n/a	n/a
43	CTCF	chr5:177558354-177558479	MCF-7	breast:	n/a	n/a
44	CTCF	chr5:177557512-177557581	Lung_OC	lung:	n/a	n/a
45	CTCF	chr5:177557500-177557650	GM12865	blood:	n/a	n/a
46	CTCF	chr5:177557500-177557650	GM12868	blood:	n/a	n/a
47	CTCF	chr5:177557446-177557534	Pancreas_OC	pancreas:	n/a	n/a
48	CTCF	chr5:177558374-177558492	GM12878	blood:	n/a	n/a
49	CTCF	chr5:177557404-177557520	MCF-7	breast:	n/a	n/a
50	CTCF	chr5:177557680-177557830	GM12868	blood:	n/a	n/a

(count:489 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:177558283-177558333	NHBE	bronchial:	n/a
2	chr5:177558283-177558333	NHBE	bronchial:	n/a
3	chr5:177558283-177558333	SK-N-MC	brain:	n/a
4	chr5:177557700-177557750	NHBE	bronchial:	n/a
5	chr5:177558283-177558333	MCF-7	breast:	n/a
6	chr5:177558253-177558303	HRPEpiC	eye:	n/a
7	chr5:177558253-177558303	IMR90	lung:	fetal
8	chr5:177557700-177557750	SKMC	muscle:	n/a
9	chr5:177558755-177558805	BE2_C	brain:	n/a
10	chr5:177558253-177558303	BE2_C	brain:	n/a
11	chr5:177557918-177557968	U87	brain:	n/a
12	chr5:177558100-177558150	HRE	kidney:	n/a
13	chr5:177558253-177558303	PrEC	prostate:	n/a
14	chr5:177558089-177558139	SKMC	muscle:	n/a
15	chr5:177558253-177558303	HCM	heart:	n/a
16	chr5:177557918-177557968	ovcar-3	ovarian:	n/a
17	chr5:177557700-177557750	HMEC	breast:	n/a
18	chr5:177558089-177558139	GM06990	blood:	n/a
19	chr5:177558283-177558333	AG04449	skin:	fetal
20	chr5:177557700-177557750	AG09319	gingival:	n/a
21	chr5:177558089-177558139	Jurkat	blood:	n/a
22	chr5:177558283-177558333	ECC-1	luminal epithelium:	n/a
23	chr5:177557700-177557750	GM12892	blood:	n/a
24	chr5:177558755-177558805	PANC-1	pancreas:	n/a
25	chr5:177558253-177558303	CMK	blood:	n/a
26	chr5:177558755-177558805	AG09319	gingival:	n/a
27	chr5:177558755-177558805	HRPEpiC	eye:	n/a
28	chr5:177558283-177558333	SKMC	muscle:	n/a
29	chr5:177558283-177558333	A549	lung:	n/a
30	chr5:177558283-177558333	GM06990	blood:	n/a
31	chr5:177557918-177557968	HepG2	liver:	n/a
32	chr5:177558100-177558150	HEK293	kidney:	embryo
33	chr5:177557819-177557869	ovcar-3	ovarian:	n/a
34	chr5:177558283-177558333	HIPEpiC	eye:	n/a
35	chr5:177558089-177558139	BE2_C	brain:	n/a
36	chr5:177557918-177557968	K562	blood:	n/a
37	chr5:177557819-177557869	NHBE	bronchial:	n/a
38	chr5:177557700-177557750	GM19239	blood:	n/a
39	chr5:177557819-177557869	K562	blood:	n/a
40	chr5:177557819-177557869	HEK293	kidney:	embryo
41	chr5:177557700-177557750	BE2_C	brain:	n/a
42	chr5:177557918-177557968	AoSMC	blood vessel:	n/a
43	chr5:177557819-177557869	AG09309	skin:	n/a
44	chr5:177558089-177558139	BJ	skin:	n/a
45	chr5:177558755-177558805	HPAEpiC	pulmonary alveolar:	n/a
46	chr5:177558253-177558303	HPAEpiC	pulmonary alveolar:	n/a
47	chr5:177558253-177558303	GM19239	blood:	n/a
48	chr5:177558089-177558139	GM12891	blood:	n/a
49	chr5:177557700-177557750	Hela-S3	cervix:	n/a
50	chr5:177558089-177558139	Caco-2	colon:	n/a

(count:17 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:177556514..177559685-chr5:177630098..177633052,4	K562	blood:
2	chr5:177558100..177560422-chr6:27113137..27116043,2	MCF-7	breast:
3	chr5:177556823..177560281-chr5:177564764..177567288,3	K562	blood:
4	chr5:177555803..177560183-chr5:177628551..177633825,8	MCF-7	breast:
5	chr5:177556550..177559096-chr5:177579482..177582645,4	K562	blood:
6	chr5:177559160..177561147-chr5:177631498..177633135,2	MCF-7	breast:
7	chr5:177556499..177561085-chr5:177629309..177633856,7	K562	blood:
8	chr5:177557386..177557994-chr7:96162492..96163492,2	HCT-116	colon:
9	chr1:28240140..28241106-chr5:177557176..177557955,2	Hela-S3	cervix:
10	chr5:176923371..176925329-chr5:177557854..177560543,2	MCF-7	breast:
11	chr5:177556060..177559089-chr5:177572421..177574313,3	K562	blood:
12	chr5:177556214..177559808-chr5:177575521..177582645,10	K562	blood:
13	chr5:177554586..177557949-chr5:177561501..177564806,6	K562	blood:
14	chr5:177556060..177559207-chr5:177571980..177574313,5	K562	blood:
15	chr11:62608645..62609556-chr5:177557343..177558256,2	NB4	blood:
16	chr17:56084693..56085358-chr5:177557758..177558549,2	Hela-S3	cervix:
17	chr5:177558236..177558903-chr5:177572730..177573529,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-N4BP3-1	chr5:177558095-177558377	NONHSAT105516

No data

Variant related genes	Relation type
RMND5B	TF binding region
RMND5B	CpG island
ENSG00000145912	chromatin interactions
ENSG00000145916	chromatin interactions
ENSG00000197451	chromatin interactions
ENSG00000184825	chromatin interactions
ENSG00000133316	chromatin interactions
ENSG00000265565	chromatin interactions
ENSG00000196923	chromatin interactions
ENSG00000197903	chromatin interactions
ENSG00000117748	chromatin interactions
ENSG00000136450	chromatin interactions

Extended variants
information (count: 108 )
Associated
traits (count: 99 )

Variant overlapped rSNPs/rCNVs (count:108 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs536982590	chr5:177556580-177556581	Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
2	rs73349806	chr5:177556615-177556616	Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs192415301	chr5:177556635-177556636	Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
4	rs533625261	chr5:177556647-177556648	Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
5	rs114189905	chr5:177556649-177556650	Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
6	rs368600032	chr5:177556660-177556661	Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
7	rs202028643	chr5:177556669-177556670	Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
8	rs548733056	chr5:177556675-177556676	Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
9	rs78527507	chr5:177556679-177556680	Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
10	rs148261376	chr5:177556680-177556681	Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
11	rs537437826	chr5:177556705-177556706	Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
12	rs555785262	chr5:177556734-177556735	Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
13	rs574366097	chr5:177556748-177556749	Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
14	rs542139789	chr5:177556752-177556753	Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
15	rs62392207	chr5:177556811-177556812	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs560053238	chr5:177556863-177556864	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
17	rs368938587	chr5:177556867-177556868	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
18	rs540331125	chr5:177556868-177556869	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
19	rs565371530	chr5:177556966-177556967	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
20	rs532700804	chr5:177557001-177557002	Weak transcription Enhancers Active TSS Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
21	rs139173699	chr5:177557009-177557010	Weak transcription Enhancers Active TSS Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs562906144	chr5:177557017-177557018	Weak transcription Enhancers Active TSS Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs530297357	chr5:177557080-177557081	Weak transcription Enhancers Active TSS Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
24	rs575109899	chr5:177557085-177557086	Weak transcription Enhancers Active TSS Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
25	rs9329130	chr5:177557107-177557108	Weak transcription Enhancers Active TSS Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
26	rs184524090	chr5:177557130-177557131	Weak transcription Enhancers Active TSS Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
27	rs9329131	chr5:177557145-177557146	Weak transcription Enhancers Active TSS Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs375796680	chr5:177557204-177557205	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
29	rs185506165	chr5:177557229-177557230	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
30	rs552392662	chr5:177557236-177557237	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
31	rs377660730	chr5:177557263-177557264	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
32	rs537575947	chr5:177557264-177557265	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
33	rs138309194	chr5:177557331-177557332	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
34	rs574386915	chr5:177557356-177557357	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
35	rs535356002	chr5:177557417-177557418	Active TSS Flanking Active TSS Enhancers Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
36	rs554047450	chr5:177557418-177557419	Active TSS Flanking Active TSS Enhancers Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
37	rs572293522	chr5:177557428-177557429	Active TSS Flanking Active TSS Enhancers Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
38	rs545977359	chr5:177557463-177557464	Active TSS Flanking Active TSS Enhancers Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
39	rs141977320	chr5:177557522-177557523	Active TSS Flanking Active TSS Enhancers Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
40	rs577401472	chr5:177557535-177557536	Active TSS Flanking Active TSS Enhancers Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
41	rs73349808	chr5:177557542-177557543	Active TSS Flanking Active TSS Enhancers Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
42	rs546779446	chr5:177557555-177557556	Active TSS Flanking Active TSS Enhancers Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
43	rs10058984	chr5:177557633-177557634	Active TSS Flanking Active TSS Bivalent/Poised TSS Enhancers Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
44	rs542116503	chr5:177557673-177557674	Active TSS Flanking Active TSS Bivalent/Poised TSS Enhancers Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
45	rs547486357	chr5:177557696-177557697	Active TSS Flanking Active TSS Bivalent/Poised TSS Enhancers Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
46	rs560830544	chr5:177557709-177557710	Active TSS Flanking Active TSS Bivalent/Poised TSS Enhancers Weak transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
47	rs115175414	chr5:177557760-177557761	Active TSS Flanking Active TSS Bivalent/Poised TSS Enhancers Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
48	rs552330923	chr5:177557786-177557787	Active TSS Flanking Active TSS Bivalent/Poised TSS Enhancers Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
49	rs145125773	chr5:177557821-177557822	Active TSS Flanking Active TSS Bivalent/Poised TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
50	rs11445687	chr5:177557826-177557827	Active TSS Flanking Active TSS Bivalent/Poised TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:99)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Medulloblastoma	21979893	CNVD
Phyllodes tumor	17334353	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	20164919	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	16751803	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Glioma	20126413	CNVD
Cancer	22429812	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Liposarcoma	21253554	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Leukemia	17361228	CNVD
Myelodysplastic syndrome	18508791	CNVD
5q-syndrome	17576883	CNVD
Gastric cancer	17908304	CNVD
Lung cancer	16740712	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Urothelial carcinoma	21177765	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
Thyroid cancer	19087340	CNVD
Acute myeloid leukemia	20729466	CNVD
lymphocytic leukemia	21291569	CNVD
Multiple myeloma	17550852	CNVD
Salivary gland tumor	18059337	CNVD
Renal cell carcinoma	19377443	CNVD
Lung cancer	18438408	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Renal cell carcinoma	18592004	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Prostate cancer	18632612	CNVD
epilepsy	18472482	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Sotos syndrome	21572526	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Sotos syndrome	17561922	CNVD
Sotos syndrome	16773131	CNVD
Mental retardation	16773131	CNVD
Sotos syndrome	22470819	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Acute myeloid leukemia	18000384	CNVD
Sudden cardiac death	19188705	CNVD
Basal cell lymphoma	16317097	CNVD
Chordoma	18071362	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Olfactory neuroblastoma	18408657	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
abnormal development	18461090	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Lung cancer	17297452	CNVD
Cancer	20164920	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21509527	CNVD
Breast cancer	21804112	CNVD
Myelofibrosis	22110671	CNVD
Sotos syndrome	22283845	CNVD
Breast cancer	16272173	CNVD
Sotos syndrome	20503325	CNVD
Lung adenocarcinoma	17086460	CNVD
Congenital Hypertrichosis Syndrome	21636067	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Breast cancer	19181860	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Ehlers-danlos syndrome	17576883	CNVD
Lung cancer	17086460	CNVD
Autism	19246517	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD

Chromatin state (count:543 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:177541800-177557200	Weak transcription	Right Atrium	heart
2	chr5:177548600-177557000	Weak transcription	Fetal Intestine Large	intestine
3	chr5:177548800-177557000	Weak transcription	Fetal Intestine Small	intestine
4	chr5:177548800-177557200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
5	chr5:177549400-177557200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
6	chr5:177549400-177558200	Weak transcription	Fetal Heart	heart
7	chr5:177549600-177557000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
8	chr5:177549600-177557200	Weak transcription	Primary hematopoietic stem cells	blood
9	chr5:177549600-177557400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
10	chr5:177550200-177557000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
11	chr5:177550400-177557200	Weak transcription	Duodenum Smooth Muscle	Duodenum
12	chr5:177550600-177557200	Weak transcription	Psoas Muscle	Psoas
13	chr5:177550800-177556800	Weak transcription	Primary B cells from cord blood	blood
14	chr5:177551400-177556800	Weak transcription	Stomach Smooth Muscle	stomach
15	chr5:177551400-177557400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
16	chr5:177551600-177557200	Weak transcription	Right Ventricle	heart
17	chr5:177551800-177557000	Weak transcription	Skeletal Muscle Female	skeletal muscle
18	chr5:177551800-177557200	Weak transcription	Brain Inferior Temporal Lobe	brain
19	chr5:177551800-177557400	Weak transcription	Spleen	Spleen
20	chr5:177552000-177557000	Weak transcription	Primary B cells from peripheral blood	blood
21	chr5:177552000-177557200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
22	chr5:177552000-177557400	Weak transcription	Stomach Mucosa	stomach
23	chr5:177552600-177556800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
24	chr5:177552800-177556800	Weak transcription	Fetal Stomach	stomach
25	chr5:177552800-177557400	Weak transcription	Esophagus	oesophagus
26	chr5:177554000-177557200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
27	chr5:177554200-177557200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
28	chr5:177554400-177556600	Weak transcription	Skeletal Muscle Male	skeletal muscle
29	chr5:177554400-177556800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
30	chr5:177554400-177557000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
31	chr5:177554400-177557400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr5:177554600-177557000	Weak transcription	Adipose Nuclei	Adipose
33	chr5:177554600-177557000	Enhancers	K562	blood
34	chr5:177554600-177557200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
35	chr5:177554600-177557200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
36	chr5:177554600-177557200	Weak transcription	HUVEC	blood vessel
37	chr5:177554600-177557400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
38	chr5:177554600-177557400	Weak transcription	Left Ventricle	heart
39	chr5:177554800-177556600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
40	chr5:177554800-177556600	Weak transcription	Fetal Muscle Trunk	muscle
41	chr5:177554800-177557200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
42	chr5:177554800-177557200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
43	chr5:177554800-177557200	Weak transcription	HUES64 Cell Line	embryonic stem cell
44	chr5:177554800-177557400	Weak transcription	H9 Cell Line	embryonic stem cell
45	chr5:177555200-177557000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
46	chr5:177555400-177557000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
47	chr5:177555800-177556600	Enhancers	iPS-15b Cell Line	embryonic stem cell
48	chr5:177555800-177556600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
49	chr5:177555800-177556600	Enhancers	NHEK	skin
50	chr5:177555800-177557000	Enhancers	ES-I3 Cell Line	embryonic stem cell

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