Variant report

Variant	nsv890634
Chromosome Location	chr8:19976239-20028474
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:19981275-19981566	K562	blood:	n/a	n/a
2	ATF1	chr8:19983232-19983316	K562	blood:	n/a	n/a
3	BCL3	chr8:19979782-19980139	A549	lung:	n/a	n/a
4	CEBPB	chr8:20002799-20003239	Hela-S3	cervix:	n/a	n/a
5	CEBPB	chr8:20002798-20003127	IMR90	lung:	n/a	n/a
6	CEBPB	chr8:19994678-19994913	HepG2	liver:	n/a	chr8:19994762-19994773
7	CEBPB	chr8:19999638-19999919	Hela-S3	cervix:	n/a	n/a
8	CEBPB	chr8:19981275-19981365	HepG2	liver:	n/a	chr8:19981303-19981314 chr8:19981301-19981314 chr8:19981301-19981312
9	CTCF	chr8:19981340-19981490	AG09309	skin:	n/a	chr8:19981419-19981437 chr8:19981421-19981434 chr8:19981425-19981434 chr8:19981414-19981435
10	CTCF	chr8:19991274-19991457	Fibrobl	skin:	n/a	chr8:19991372-19991390 chr8:19991367-19991388 chr8:19991373-19991389 chr8:19991374-19991387
11	CTCF	chr8:19981380-19981530	GM12866	blood:	n/a	chr8:19981419-19981437 chr8:19981421-19981434 chr8:19981425-19981434 chr8:19981414-19981435
12	CTCF	chr8:20011944-20011960	GM20000	blood:	n/a	n/a
13	CTCF	chr8:19990980-19991130	HMEC	breast:	n/a	n/a
14	CTCF	chr8:19991300-19991450	AoAF	blood vessel:	n/a	chr8:19991372-19991390 chr8:19991367-19991388 chr8:19991373-19991389 chr8:19991374-19991387
15	CTCF	chr8:19991300-19991450	WERI-Rb-1	eye:	n/a	chr8:19991372-19991390 chr8:19991367-19991388 chr8:19991373-19991389 chr8:19991374-19991387
16	CTCF	chr8:19992020-19992170	AG09319	gingival:	n/a	n/a
17	CTCF	chr8:19981340-19981490	HMF	breast:	n/a	chr8:19981419-19981437 chr8:19981421-19981434 chr8:19981425-19981434 chr8:19981414-19981435
18	CTCF	chr8:19991320-19991470	GM12870	blood:	n/a	chr8:19991372-19991390 chr8:19991367-19991388 chr8:19991373-19991389 chr8:19991374-19991387
19	CTCF	chr8:19991291-19991435	GM19239	blood:	n/a	chr8:19991372-19991390 chr8:19991367-19991388 chr8:19991373-19991389 chr8:19991374-19991387
20	CTCF	chr8:19981245-19981599	GM12878	blood:	n/a	chr8:19981419-19981437 chr8:19981421-19981434 chr8:19981425-19981434 chr8:19981414-19981435
21	CTCF	chr8:19981268-19981573	HepG2	liver:	n/a	chr8:19981419-19981437 chr8:19981421-19981434 chr8:19981425-19981434 chr8:19981414-19981435
22	CTCF	chr8:19981980-19982130	HMEC	breast:	n/a	n/a
23	CTCF	chr8:19981220-19981370	HFF	foreskin:	n/a	n/a
24	CTCF	chr8:19981320-19981470	HCPEpiC	choroid plexus:	n/a	chr8:19981419-19981437 chr8:19981421-19981434 chr8:19981425-19981434 chr8:19981414-19981435
25	CTCF	chr8:19991340-19991490	GM12869	blood:	n/a	chr8:19991372-19991390 chr8:19991367-19991388 chr8:19991373-19991389 chr8:19991374-19991387
26	CTCF	chr8:19981280-19981430	GM12864	blood:	n/a	n/a
27	CTCF	chr8:19991300-19991450	GM12875	blood:	n/a	chr8:19991372-19991390 chr8:19991367-19991388 chr8:19991373-19991389 chr8:19991374-19991387
28	CTCF	chr8:19991300-19991450	AG04449	skin:	n/a	chr8:19991372-19991390 chr8:19991367-19991388 chr8:19991373-19991389 chr8:19991374-19991387
29	CTCF	chr8:19991300-19991450	A549	lung:	n/a	chr8:19991372-19991390 chr8:19991367-19991388 chr8:19991373-19991389 chr8:19991374-19991387
30	CTCF	chr8:19981340-19981490	NHEK	skin:	n/a	chr8:19981419-19981437 chr8:19981421-19981434 chr8:19981425-19981434 chr8:19981414-19981435
31	CTCF	chr8:19991265-19991506	Pancreas_OC	pancreas:	n/a	chr8:19991372-19991390 chr8:19991367-19991388 chr8:19991373-19991389 chr8:19991374-19991387
32	CTCF	chr8:19991300-19991450	GM06990	blood:	n/a	chr8:19991372-19991390 chr8:19991367-19991388 chr8:19991373-19991389 chr8:19991374-19991387
33	CTCF	chr8:19991245-19991511	Gliobla	brain:	n/a	chr8:19991372-19991390 chr8:19991367-19991388 chr8:19991373-19991389 chr8:19991374-19991387
34	CTCF	chr8:19991241-19991532	K562	blood:	n/a	chr8:19991372-19991390 chr8:19991367-19991388 chr8:19991373-19991389 chr8:19991374-19991387
35	CTCF	chr8:19981292-19981513	A549	lung:	n/a	chr8:19981419-19981437 chr8:19981421-19981434 chr8:19981425-19981434 chr8:19981414-19981435
36	CTCF	chr8:19991302-19991523	GM20000	blood:	n/a	chr8:19991372-19991390 chr8:19991367-19991388 chr8:19991373-19991389 chr8:19991374-19991387
37	CTCF	chr8:19981300-19981450	HRE	kidney:	n/a	chr8:19981419-19981437 chr8:19981421-19981434 chr8:19981425-19981434 chr8:19981414-19981435
38	CTCF	chr8:19991260-19991410	GM12875	blood:	n/a	chr8:19991372-19991390 chr8:19991367-19991388 chr8:19991373-19991389 chr8:19991374-19991387
39	CTCF	chr8:19991280-19991430	HEEpiC	esophagus:	n/a	chr8:19991372-19991390 chr8:19991367-19991388 chr8:19991373-19991389 chr8:19991374-19991387
40	CTCF	chr8:19991300-19991450	GM12873	blood:	n/a	chr8:19991372-19991390 chr8:19991367-19991388 chr8:19991373-19991389 chr8:19991374-19991387
41	CTCF	chr8:19981302-19981492	SK-N-SH_RA	brain:	n/a	chr8:19981419-19981437 chr8:19981421-19981434 chr8:19981425-19981434 chr8:19981414-19981435
42	CTCF	chr8:19981300-19981450	Hela-S3	cervix:	n/a	chr8:19981419-19981437 chr8:19981421-19981434 chr8:19981425-19981434 chr8:19981414-19981435
43	CTCF	chr8:19981360-19981510	Caco-2	colon:	n/a	chr8:19981419-19981437 chr8:19981421-19981434 chr8:19981425-19981434 chr8:19981414-19981435
44	CTCF	chr8:19991300-19991450	AG10803	skin:	n/a	chr8:19991372-19991390 chr8:19991367-19991388 chr8:19991373-19991389 chr8:19991374-19991387
45	CTCF	chr8:19981340-19981490	GM12865	blood:	n/a	chr8:19981419-19981437 chr8:19981421-19981434 chr8:19981425-19981434 chr8:19981414-19981435
46	CTCF	chr8:19991280-19991430	AG04450	lung:	n/a	chr8:19991372-19991390 chr8:19991367-19991388 chr8:19991373-19991389 chr8:19991374-19991387
47	CTCF	chr8:19990940-19991090	AoAF	blood vessel:	n/a	n/a
48	CTCF	chr8:19991340-19991490	GM12868	blood:	n/a	chr8:19991372-19991390 chr8:19991367-19991388 chr8:19991373-19991389 chr8:19991374-19991387
49	CTCF	chr8:19991280-19991430	NHDF-neo	bronchial:	n/a	chr8:19991372-19991390 chr8:19991367-19991388 chr8:19991373-19991389 chr8:19991374-19991387
50	CTCF	chr8:19991100-19991564	A549	lung:	n/a	chr8:19991372-19991390 chr8:19991367-19991388 chr8:19991373-19991389 chr8:19991374-19991387

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:20010728-20010778	HNPCEpiC	eye:	n/a
2	chr8:20010728-20010778	HNPCEpiC	eye:	n/a
3	chr8:20010728-20010778	GM19239	blood:	n/a
4	chr8:20010728-20010778	NHBE	bronchial:	n/a
5	chr8:20010728-20010778	H1-hESC	embryonic stem cell:	embryo
6	chr8:20010728-20010778	ovcar-3	ovarian:	n/a
7	chr8:19980910-19980960	AG04449	skin:	fetal
8	chr8:20010728-20010778	HEK293	kidney:	embryo
9	chr8:20002826-20002876	Jurkat	blood:	n/a
10	chr8:19980910-19980960	Jurkat	blood:	n/a
11	chr8:20010728-20010778	HCM	heart:	n/a
12	chr8:20002826-20002876	GM06990	blood:	n/a
13	chr8:19980910-19980960	AG09309	skin:	n/a
14	chr8:20010728-20010778	LNCaP	prostate:	n/a
15	chr8:20010728-20010778	HRE	kidney:	n/a
16	chr8:20010728-20010778	NT2-D1	testis:	n/a
17	chr8:20010728-20010778	RPTEC	kidney:	n/a
18	chr8:20002826-20002876	Caco-2	colon:	n/a
19	chr8:20002826-20002876	NB4	blood:	n/a
20	chr8:19980910-19980960	PrEC	prostate:	n/a
21	chr8:20002826-20002876	GM12878	blood:	n/a
22	chr8:19980910-19980960	U87	brain:	n/a
23	chr8:20010728-20010778	A549	lung:	n/a
24	chr8:19980910-19980960	HRPEpiC	eye:	n/a
25	chr8:20002826-20002876	AG09319	gingival:	n/a
26	chr8:20010728-20010778	AG09309	skin:	n/a
27	chr8:19980910-19980960	HCM	heart:	n/a
28	chr8:20002826-20002876	MCF-7	breast:	n/a
29	chr8:19980910-19980960	PANC-1	pancreas:	n/a
30	chr8:20002826-20002876	HCPEpiC	choroid plexus:	n/a
31	chr8:19980910-19980960	GM12892	blood:	n/a
32	chr8:20010728-20010778	BJ	skin:	n/a
33	chr8:20002826-20002876	Hepatocyte	liver:	n/a
34	chr8:20002826-20002876	PrEC	prostate:	n/a
35	chr8:19980910-19980960	BJ	skin:	n/a
36	chr8:20010728-20010778	IMR90	lung:	fetal
37	chr8:20002826-20002876	H1-hESC	embryonic stem cell:	embryo
38	chr8:20002826-20002876	ovcar-3	ovarian:	n/a
39	chr8:20010728-20010778	PrEC	prostate:	n/a
40	chr8:20002826-20002876	HNPCEpiC	eye:	n/a
41	chr8:20010728-20010778	HIPEpiC	eye:	n/a
42	chr8:20010728-20010778	MCF10A-Er-Src	breast:	n/a
43	chr8:20010728-20010778	SK-N-MC	brain:	n/a
44	chr8:20002826-20002876	HL-60	blood:	n/a
45	chr8:20002826-20002876	HEK293	kidney:	embryo
46	chr8:20010728-20010778	MCF-7	breast:	n/a
47	chr8:20010728-20010778	Jurkat	blood:	n/a
48	chr8:20010728-20010778	PANC-1	pancreas:	n/a
49	chr8:19980910-19980960	RPTEC	kidney:	n/a
50	chr8:20010728-20010778	K562	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr8:20020373..20021951-chr8:20028843..20031840,2	MCF-7	breast:
2	chr8:19980514..19983511-chr8:19986584..19989159,2	K562	blood:
3	chr8:19991226..19991903-chr8:20233790..20234437,2	MCF-7	breast:
4	chr8:20007650..20009745-chr8:20016355..20018698,2	K562	blood:
5	chr8:19229314..19230191-chr8:19990957..19991686,3	K562	blood:
6	chr8:19786443..19786979-chr8:19980934..19981886,2	MCF-7	breast:
7	chr8:19674771..19677183-chr8:19988400..19991254,2	K562	blood:
8	chr8:19727572..19728249-chr8:19990904..19991781,3	K562	blood:
9	chr8:19980514..19983511-chr8:19986584..19989159,2	K562	blood:
10	chr8:19614946..19615490-chr8:19990822..19991486,2	MCF-7	breast:
11	chr8:20007650..20009376-chr8:20017198..20019566,2	K562	blood:
12	chr8:19786061..19786740-chr8:19980944..19981679,3	K562	blood:
13	chr8:20026355..20028616-chr8:20204009..20206299,2	K562	blood:
14	chr8:19670534..19671042-chr8:19990928..19991891,2	MCF-7	breast:
15	chr8:19727405..19728444-chr8:19980912..19981476,3	MCF-7	breast:

Variant related genes	Relation type
SLC18A1	TF binding region
SLC18A1	CpG island
ENSG00000147408	chromatin interactions
ENSG00000036565	chromatin interactions
ENSG00000104613	chromatin interactions

Extended variants
information (count: 2838 )
Associated
traits (count: 117 )

Variant overlapped rSNPs/rCNVs (count:2838 , 50 per page) page: 1 2 3 4 5 6 7 ... 57

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10107943	chr8:19976239-19976240	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs540994958	chr8:19976270-19976271	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs116490709	chr8:19976279-19976280	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs376164057	chr8:19976290-19976291	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs191780237	chr8:19976334-19976335	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs566950658	chr8:19976344-19976345	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs563404038	chr8:19976372-19976373	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs530951045	chr8:19976375-19976376	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs549552578	chr8:19976385-19976386	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs369200348	chr8:19976387-19976388	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs184023080	chr8:19976388-19976389	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs528767137	chr8:19976394-19976395	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs115936046	chr8:19976414-19976415	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs143171668	chr8:19976451-19976452	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs539393301	chr8:19976467-19976468	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs370803115	chr8:19976492-19976493	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs188904586	chr8:19976495-19976496	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs112358528	chr8:19976496-19976497	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs536792076	chr8:19976515-19976516	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs558631006	chr8:19976543-19976544	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs148198242	chr8:19976557-19976558	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs114887552	chr8:19976616-19976617	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs552818001	chr8:19976684-19976685	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs577517113	chr8:19976690-19976691	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs544994458	chr8:19976691-19976692	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs563391912	chr8:19976728-19976729	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs531015102	chr8:19976741-19976742	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs542791623	chr8:19976799-19976800	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs141143457	chr8:19976811-19976812	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
30	rs11994862	chr8:19976816-19976817	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	mRNA abundance
31	rs547218348	chr8:19976842-19976843	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
32	rs571930389	chr8:19976848-19976849	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
33	rs532897116	chr8:19976853-19976854	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
34	rs192637501	chr8:19976873-19976874	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
35	rs114400371	chr8:19976915-19976916	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
36	rs537133873	chr8:19976917-19976918	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
37	rs548767382	chr8:19976949-19976950	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
38	rs35310326	chr8:19976963-19976964	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
39	rs534461569	chr8:19976972-19976973	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
40	rs78588811	chr8:19976992-19976993	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
41	rs577515418	chr8:19976994-19976995	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
42	rs182154187	chr8:19977016-19977017	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
43	rs556923481	chr8:19977018-19977019	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
44	rs186835289	chr8:19977030-19977031	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
45	rs17411601	chr8:19977043-19977044	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
46	rs117741679	chr8:19977049-19977050	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
47	rs138012843	chr8:19977061-19977062	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
48	rs367945599	chr8:19977074-19977075	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
49	rs371778674	chr8:19977110-19977111	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
50	rs143476740	chr8:19977128-19977129	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:117)

Disease	PMID	Source
Multiple myeloma	16616336	CNVD
Hepatocellular carcinoma	22174799	CNVD
Heart disease	21282601	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	16573809	CNVD
T-cell lymphomas	19863542	CNVD
Ovarian cancer	22174824	CNVD
Colorectal cancer	21297112	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Salivary gland tumor	18059337	CNVD
Breast cancer	17133270	CNVD
Melanoma	18172304	CNVD
Medulloblastoma	21979893	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Breast cancer	17393978	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	21637783	CNVD
Breast cancer	20837533	CNVD
Squamous cell cancer	21044232	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	22429812	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Basal cell lymphoma	21115979	CNVD
Breast cancer	21264507	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Oral cancer	21386901	CNVD
Prostate cancer	21088497	CNVD
Prostate cancer	21965145	CNVD
Breast cancer	20940404	CNVD
Colorectal cancer	19359472	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Gastric cancer	17167181	CNVD
Prostate cancer	16705090	CNVD
8p-syndrome	17576883	CNVD
Colorectal cancer	16272173	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	16968546	CNVD
Lung adenocarcinoma	19525976	CNVD
Lung cancer	19525976	CNVD
Prostate cancer	17245344	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Cancer	16751803	CNVD
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	CNVD
Autism	19415332	CNVD
Malaria	21533027	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Esophageal cancer	21851588	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Breast cancer	21785460	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21509527	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	16608533	CNVD
Seminomas	18059402	CNVD
Lung cancer	18438408	CNVD
Medulloblastoma	16783165	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Myxofibrosarcoma	16751306	CNVD
Immune disease	21572526	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Kallmann Syndrome 2	22470819	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Epilepsy	22083797	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Myelofibrosis	22110671	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	17603634	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Bladder cancer	21909424	CNVD
Multiple myeloma	17550852	CNVD
Pancreatic cancer	21811587	CNVD
Multiple myeloma	16461302	CNVD
Developmental delay	21373258	CNVD
Thyroid cancer	19087340	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	21364760	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Cancer	18840272	CNVD
Breast cancer	19602461	CNVD
Osteosarcoma	19286668	CNVD
Prostate cancer	19242612	CNVD
Prostate cancer	19258508	CNVD
small cell lung cancer	20016488	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Gastric adenocarcinoma	19115996	CNVD
Colorectal cancer	19455253	CNVD
Melanoma	20688739	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Prostate cancer	22341455	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:387 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:19969200-19976800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr8:19969800-19976800	Weak transcription	Hela-S3	cervix
3	chr8:19970000-19977400	Weak transcription	Right Atrium	heart
4	chr8:19970400-19976800	Weak transcription	Left Ventricle	heart
5	chr8:19971400-19976800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr8:19971400-19976800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
7	chr8:19971400-19976800	Weak transcription	Fetal Muscle Trunk	muscle
8	chr8:19971400-19977400	Weak transcription	Psoas Muscle	Psoas
9	chr8:19971600-19977800	Weak transcription	Skeletal Muscle Male	skeletal muscle
10	chr8:19972200-19977400	Weak transcription	Fetal Muscle Leg	muscle
11	chr8:19972600-19977000	Weak transcription	Colon Smooth Muscle	Colon
12	chr8:19973000-19976600	Weak transcription	H9 Cell Line	embryonic stem cell
13	chr8:19973200-19976800	Weak transcription	Adipose Nuclei	Adipose
14	chr8:19973200-19977400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
15	chr8:19973400-19976800	Weak transcription	HUVEC	blood vessel
16	chr8:19974200-19979200	Enhancers	Placenta	Placenta
17	chr8:19975600-19976800	Weak transcription	Placenta Amnion	Placenta Amnion
18	chr8:19975600-19977200	Weak transcription	HMEC	breast
19	chr8:19975800-19977200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
20	chr8:19975800-19980000	Weak transcription	NHEK	skin
21	chr8:19976200-19978400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
22	chr8:19976800-19977000	Bivalent Enhancer	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
23	chr8:19976800-19977000	Enhancers	Fetal Muscle Trunk	muscle
24	chr8:19976800-19977000	Enhancers	Lung	lung
25	chr8:19976800-19977000	Enhancers	Placenta Amnion	Placenta Amnion
26	chr8:19976800-19977000	Bivalent Enhancer	HSMM	muscle
27	chr8:19976800-19977200	Enhancers	Hela-S3	cervix
28	chr8:19976800-19977400	Bivalent Enhancer	Muscle Satellite Cultured Cells	--
29	chr8:19976800-19977600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
30	chr8:19976800-19977600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
31	chr8:19976800-19977600	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
32	chr8:19976800-19977600	Enhancers	Liver	Liver
33	chr8:19976800-19977600	Enhancers	Fetal Stomach	stomach
34	chr8:19976800-19977600	Bivalent Enhancer	Osteobl	bone
35	chr8:19976800-19978000	Enhancers	HUVEC	blood vessel
36	chr8:19976800-19978200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
37	chr8:19976800-19978200	Bivalent Enhancer	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
38	chr8:19976800-19978200	Enhancers	Adipose Nuclei	Adipose
39	chr8:19976800-19978200	Enhancers	Left Ventricle	heart
40	chr8:19976800-19978400	Enhancers	A549	lung
41	chr8:19976800-19978600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
42	chr8:19976800-19978600	Enhancers	NH-A	brain
43	chr8:19977000-19977400	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
44	chr8:19977000-19977400	Weak transcription	Placenta Amnion	Placenta Amnion
45	chr8:19977000-19977600	Weak transcription	Fetal Muscle Trunk	muscle
46	chr8:19977000-19978000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
47	chr8:19977000-19978000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
48	chr8:19977000-19978000	Enhancers	Colon Smooth Muscle	Colon
49	chr8:19977000-19978000	Weak transcription	Lung	lung
50	chr8:19977000-19978000	Enhancers	HSMM	muscle

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