Variant report

Variant	esv2759602
Chromosome Location	chr8:19986571-20029603
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	CEBPB	chr8:19999638-19999919	Hela-S3	cervix:	n/a	n/a
2	CEBPB	chr8:20002799-20003239	Hela-S3	cervix:	n/a	n/a
3	CEBPB	chr8:20002798-20003127	IMR90	lung:	n/a	n/a
4	CEBPB	chr8:19994678-19994913	HepG2	liver:	n/a	chr8:19994762-19994773
5	CTCF	chr8:19991300-19991450	HPF	lung:	n/a	chr8:19991372-19991390 chr8:19991367-19991388 chr8:19991373-19991389 chr8:19991374-19991387
6	CTCF	chr8:19991300-19991450	HAc	cerebellar:	n/a	chr8:19991372-19991390 chr8:19991367-19991388 chr8:19991373-19991389 chr8:19991374-19991387
7	CTCF	chr8:19991245-19991511	Gliobla	brain:	n/a	chr8:19991372-19991390 chr8:19991367-19991388 chr8:19991373-19991389 chr8:19991374-19991387
8	CTCF	chr8:19991320-19991470	NHEK	skin:	n/a	chr8:19991372-19991390 chr8:19991367-19991388 chr8:19991373-19991389 chr8:19991374-19991387
9	CTCF	chr8:19991320-19991470	AG04449	skin:	n/a	chr8:19991372-19991390 chr8:19991367-19991388 chr8:19991373-19991389 chr8:19991374-19991387
10	CTCF	chr8:19991340-19991490	MCF-7	breast:	n/a	chr8:19991372-19991390 chr8:19991367-19991388 chr8:19991373-19991389 chr8:19991374-19991387
11	CTCF	chr8:19991302-19991523	GM20000	blood:	n/a	chr8:19991372-19991390 chr8:19991367-19991388 chr8:19991373-19991389 chr8:19991374-19991387
12	CTCF	chr8:19988620-19988770	HPF	lung:	n/a	n/a
13	CTCF	chr8:20027833-20027913	K562	blood:	n/a	n/a
14	CTCF	chr8:19991329-19991398	MCF-7	breast:	n/a	chr8:19991372-19991390 chr8:19991367-19991388 chr8:19991373-19991389 chr8:19991374-19991387
15	CTCF	chr8:20027847-20028005	K562	blood:	n/a	n/a
16	CTCF	chr8:19991300-19991450	HRPEpiC	eye:	n/a	chr8:19991372-19991390 chr8:19991367-19991388 chr8:19991373-19991389 chr8:19991374-19991387
17	CTCF	chr8:19991300-19991450	GM12875	blood:	n/a	chr8:19991372-19991390 chr8:19991367-19991388 chr8:19991373-19991389 chr8:19991374-19991387
18	CTCF	chr8:19990984-19991650	SK-N-SH	brain:	n/a	chr8:19991372-19991390 chr8:19991367-19991388 chr8:19991373-19991389 chr8:19991374-19991387
19	CTCF	chr8:19991300-19991450	Hela-S3	cervix:	n/a	chr8:19991372-19991390 chr8:19991367-19991388 chr8:19991373-19991389 chr8:19991374-19991387
20	CTCF	chr8:19991300-19991450	HMF	breast:	n/a	chr8:19991372-19991390 chr8:19991367-19991388 chr8:19991373-19991389 chr8:19991374-19991387
21	CTCF	chr8:19991280-19991430	AG04450	lung:	n/a	chr8:19991372-19991390 chr8:19991367-19991388 chr8:19991373-19991389 chr8:19991374-19991387
22	CTCF	chr8:19990900-19991050	AG04450	lung:	n/a	n/a
23	CTCF	chr8:19991280-19991430	HRE	kidney:	n/a	chr8:19991372-19991390 chr8:19991367-19991388 chr8:19991373-19991389 chr8:19991374-19991387
24	CTCF	chr8:19991300-19991450	HEK293	kidney:	n/a	chr8:19991372-19991390 chr8:19991367-19991388 chr8:19991373-19991389 chr8:19991374-19991387
25	CTCF	chr8:19991320-19991470	WERI-Rb-1	eye:	n/a	chr8:19991372-19991390 chr8:19991367-19991388 chr8:19991373-19991389 chr8:19991374-19991387
26	CTCF	chr8:19991320-19991470	AG09319	gingival:	n/a	chr8:19991372-19991390 chr8:19991367-19991388 chr8:19991373-19991389 chr8:19991374-19991387
27	CTCF	chr8:19991240-19991390	NHDF-neo	bronchial:	n/a	chr8:19991372-19991390 chr8:19991367-19991388 chr8:19991373-19991389 chr8:19991374-19991387
28	CTCF	chr8:20022260-20022410	WERI-Rb-1	eye:	n/a	n/a
29	CTCF	chr8:19991300-19991450	WERI-Rb-1	eye:	n/a	chr8:19991372-19991390 chr8:19991367-19991388 chr8:19991373-19991389 chr8:19991374-19991387
30	CTCF	chr8:19991300-19991450	AG04449	skin:	n/a	chr8:19991372-19991390 chr8:19991367-19991388 chr8:19991373-19991389 chr8:19991374-19991387
31	CTCF	chr8:19991280-19991430	HEEpiC	esophagus:	n/a	chr8:19991372-19991390 chr8:19991367-19991388 chr8:19991373-19991389 chr8:19991374-19991387
32	CTCF	chr8:19991300-19991450	GM12868	blood:	n/a	chr8:19991372-19991390 chr8:19991367-19991388 chr8:19991373-19991389 chr8:19991374-19991387
33	CTCF	chr8:19991300-19991450	AG09309	skin:	n/a	chr8:19991372-19991390 chr8:19991367-19991388 chr8:19991373-19991389 chr8:19991374-19991387
34	CTCF	chr8:19991262-19991453	A549	lung:	n/a	chr8:19991372-19991390 chr8:19991367-19991388 chr8:19991373-19991389 chr8:19991374-19991387
35	CTCF	chr8:19991214-19991509	K562	blood:	n/a	chr8:19991372-19991390 chr8:19991367-19991388 chr8:19991373-19991389 chr8:19991374-19991387
36	CTCF	chr8:19991300-19991450	GM12867	blood:	n/a	chr8:19991372-19991390 chr8:19991367-19991388 chr8:19991373-19991389 chr8:19991374-19991387
37	CTCF	chr8:19991280-19991430	HL-60	blood:	n/a	chr8:19991372-19991390 chr8:19991367-19991388 chr8:19991373-19991389 chr8:19991374-19991387
38	CTCF	chr8:19990803-19990822	Medullo	brain:	n/a	n/a
39	CTCF	chr8:19999520-19999670	HMEC	breast:	n/a	n/a
40	CTCF	chr8:19991205-19991478	SK-N-SH_RA	brain:	n/a	chr8:19991372-19991390 chr8:19991367-19991388 chr8:19991373-19991389 chr8:19991374-19991387
41	CTCF	chr8:19991300-19991450	AG09319	gingival:	n/a	chr8:19991372-19991390 chr8:19991367-19991388 chr8:19991373-19991389 chr8:19991374-19991387
42	CTCF	chr8:19991260-19991410	HMF	breast:	n/a	chr8:19991372-19991390 chr8:19991367-19991388 chr8:19991373-19991389 chr8:19991374-19991387
43	CTCF	chr8:19991280-19991430	BJ	skin:	n/a	chr8:19991372-19991390 chr8:19991367-19991388 chr8:19991373-19991389 chr8:19991374-19991387
44	CTCF	chr8:19991300-19991450	HCPEpiC	choroid plexus:	n/a	chr8:19991372-19991390 chr8:19991367-19991388 chr8:19991373-19991389 chr8:19991374-19991387
45	CTCF	chr8:19990835-19990845	Medullo	brain:	n/a	n/a
46	CTCF	chr8:19990920-19991070	HMF	breast:	n/a	n/a
47	CTCF	chr8:19991280-19991430	MCF-7	breast:	n/a	chr8:19991372-19991390 chr8:19991367-19991388 chr8:19991373-19991389 chr8:19991374-19991387
48	CTCF	chr8:19991703-19991730	GM10248	blood:	n/a	n/a
49	CTCF	chr8:19991300-19991450	BE2_C	brain:	n/a	chr8:19991372-19991390 chr8:19991367-19991388 chr8:19991373-19991389 chr8:19991374-19991387
50	CTCF	chr8:20022323-20022463	Gliobla	brain:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:20002826-20002876	HPAEpiC	pulmonary alveolar:	n/a
2	chr8:20010728-20010778	HRPEpiC	eye:	n/a
3	chr8:20010728-20010778	AG04450	lung:	fetal
4	chr8:20010728-20010778	K562	blood:	n/a
5	chr8:20010728-20010778	BJ	skin:	n/a
6	chr8:20010728-20010778	GM12892	blood:	n/a
7	chr8:20010728-20010778	Hela-S3	cervix:	n/a
8	chr8:20010728-20010778	GM12878	blood:	n/a
9	chr8:20002826-20002876	NT2-D1	testis:	n/a
10	chr8:20010728-20010778	GM19239	blood:	n/a
11	chr8:20002826-20002876	AoSMC	blood vessel:	n/a
12	chr8:20002826-20002876	HNPCEpiC	eye:	n/a
13	chr8:20002826-20002876	Jurkat	blood:	n/a
14	chr8:20010728-20010778	AG10803	skin:	n/a
15	chr8:20002826-20002876	ECC-1	luminal epithelium:	n/a
16	chr8:20002826-20002876	NB4	blood:	n/a
17	chr8:20010728-20010778	HRE	kidney:	n/a
18	chr8:20010728-20010778	HRCEpiC	kidney:	n/a
19	chr8:20002826-20002876	SAEC	small airway:	n/a
20	chr8:20002826-20002876	SKMC	muscle:	n/a
21	chr8:20002826-20002876	GM12878	blood:	n/a
22	chr8:20010728-20010778	IMR90	lung:	fetal
23	chr8:20010728-20010778	Caco-2	colon:	n/a
24	chr8:20002826-20002876	T-47D	breast:	n/a
25	chr8:20002826-20002876	HUVEC	blood vessel:	n/a
26	chr8:20010728-20010778	LNCaP	prostate:	n/a
27	chr8:20010728-20010778	GM12891	blood:	n/a
28	chr8:20010728-20010778	MCF-7	breast:	n/a
29	chr8:20010728-20010778	SAEC	small airway:	n/a
30	chr8:20010728-20010778	SK-N-SH	brain:	n/a
31	chr8:20010728-20010778	NH-A	brain:	n/a
32	chr8:20002826-20002876	AG09309	skin:	n/a
33	chr8:20002826-20002876	H1-hESC	embryonic stem cell:	embryo
34	chr8:20002826-20002876	SK-N-MC	brain:	n/a
35	chr8:20010728-20010778	HCPEpiC	choroid plexus:	n/a
36	chr8:20010728-20010778	PrEC	prostate:	n/a
37	chr8:20010728-20010778	CMK	blood:	n/a
38	chr8:20010728-20010778	SK-N-SH_RA	brain:	n/a
39	chr8:20010728-20010778	HMEC	breast:	n/a
40	chr8:20002826-20002876	PrEC	prostate:	n/a
41	chr8:20010728-20010778	RPTEC	kidney:	n/a
42	chr8:20010728-20010778	NB4	blood:	n/a
43	chr8:20002826-20002876	HepG2	liver:	n/a
44	chr8:20010728-20010778	MCF10A-Er-Src	breast:	n/a
45	chr8:20002826-20002876	HRE	kidney:	n/a
46	chr8:20002826-20002876	AG04450	lung:	fetal
47	chr8:20010728-20010778	GM06990	blood:	n/a
48	chr8:20010728-20010778	HAEpiC	amniotic membrane:	n/a
49	chr8:20010728-20010778	ECC-1	luminal epithelium:	n/a
50	chr8:20010728-20010778	NHDF-neo	bronchial:	n/a

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

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

Extended variants
information (count: 2409 )
Associated
traits (count: 117 )

Variant overlapped rSNPs/rCNVs (count:2409 , 50 per page) page: 1 2 3 4 5 6 7 ... 49

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs17092046	chr8:19986571-19986572	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs551829098	chr8:19986583-19986584	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs190898325	chr8:19986609-19986610	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs577517054	chr8:19986652-19986653	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs182434141	chr8:19986655-19986656	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs138281286	chr8:19986660-19986661	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs17092048	chr8:19986669-19986670	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs376153276	chr8:19986690-19986691	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs548744401	chr8:19986696-19986697	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs185771169	chr8:19986705-19986706	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs528297429	chr8:19986717-19986718	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs531279772	chr8:19986721-19986722	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs374574186	chr8:19986736-19986737	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs571460506	chr8:19986747-19986748	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs539014149	chr8:19986789-19986790	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs551043978	chr8:19986808-19986809	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs569354691	chr8:19986811-19986812	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs116336629	chr8:19986845-19986846	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs191223404	chr8:19986866-19986867	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs567801650	chr8:19986868-19986869	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs182967028	chr8:19986888-19986889	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs114822606	chr8:19986912-19986913	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs577505531	chr8:19986920-19986921	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs564877902	chr8:19986933-19986934	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs149611002	chr8:19986935-19986936	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs562972060	chr8:19986940-19986941	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs574979535	chr8:19986974-19986975	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs547054719	chr8:19986975-19986976	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs139009100	chr8:19986988-19986989	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs188412965	chr8:19986996-19986997	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs528248869	chr8:19987007-19987008	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs190422755	chr8:19987042-19987043	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs539023821	chr8:19987050-19987051	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs532334683	chr8:19987076-19987077	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs532717668	chr8:19987086-19987087	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs550980459	chr8:19987091-19987092	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs569244115	chr8:19987092-19987093	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs536669890	chr8:19987123-19987124	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs146301671	chr8:19987149-19987150	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs10503671	chr8:19987173-19987174	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs576246484	chr8:19987179-19987180	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs371348884	chr8:19987180-19987181	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs373776804	chr8:19987193-19987194	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs182776626	chr8:19987224-19987225	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs187422889	chr8:19987225-19987226	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs537307855	chr8:19987239-19987240	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs556454414	chr8:19987246-19987247	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs192330739	chr8:19987250-19987251	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs185691772	chr8:19987251-19987252	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs554640610	chr8:19987310-19987311	Enhancers Weak transcription	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:225 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:19978000-19993600	Weak transcription	Right Ventricle	heart
2	chr8:19978200-19987000	Weak transcription	Left Ventricle	heart
3	chr8:19985800-19987200	Enhancers	HMEC	breast
4	chr8:19985800-19987600	Enhancers	Placenta	Placenta
5	chr8:19985800-19988000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr8:19986000-19987200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr8:19986000-19987200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
8	chr8:19986000-19987400	Enhancers	NHEK	skin
9	chr8:19986000-19987600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
10	chr8:19986000-19988000	Enhancers	Placenta Amnion	Placenta Amnion
11	chr8:19986400-19986800	Weak transcription	Esophagus	oesophagus
12	chr8:19986600-19987200	Enhancers	Breast Myoepithelial Primary Cells	Breast
13	chr8:19986600-19987400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
14	chr8:19986800-19987000	Enhancers	Esophagus	oesophagus
15	chr8:19987000-19987800	Enhancers	Left Ventricle	heart
16	chr8:19987000-19992400	Weak transcription	Esophagus	oesophagus
17	chr8:19987200-19992600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
18	chr8:19987200-19992600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
19	chr8:19987200-19995000	Weak transcription	HMEC	breast
20	chr8:19987400-19992200	Weak transcription	NHEK	skin
21	chr8:19987600-19988000	Bivalent Enhancer	Placenta	Placenta
22	chr8:19987600-19992400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
23	chr8:19988000-19992800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
24	chr8:19990000-19990200	Enhancers	iPS-20b Cell Line	embryonic stem cell
25	chr8:19992200-19993600	Enhancers	NHEK	skin
26	chr8:19992400-19993000	Enhancers	Esophagus	oesophagus
27	chr8:19992400-19993600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
28	chr8:19992600-19993200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
29	chr8:19992600-19993200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
30	chr8:19992800-19993000	Enhancers	ES-I3 Cell Line	embryonic stem cell
31	chr8:19992800-19993000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
32	chr8:19992800-19993000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
33	chr8:19992800-19993200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
34	chr8:19992800-19993200	Enhancers	Fetal Intestine Large	intestine
35	chr8:19993000-19993200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
36	chr8:19993000-19993400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
37	chr8:19993000-19993800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
38	chr8:19993000-19995000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
39	chr8:19993000-19999400	Weak transcription	Esophagus	oesophagus
40	chr8:19993200-19993600	Weak transcription	Fetal Intestine Large	intestine
41	chr8:19993200-19995000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
42	chr8:19993200-19995400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
43	chr8:19993200-19998400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
44	chr8:19993200-20000400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
45	chr8:19993400-19994200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
46	chr8:19993600-19993800	Enhancers	Right Ventricle	heart
47	chr8:19993600-19994200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
48	chr8:19993600-19994200	Enhancers	Fetal Intestine Large	intestine
49	chr8:19993600-19995000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
50	chr8:19993600-19995000	Weak transcription	NHEK	skin

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