Variant report

Variant	nsv916709
Chromosome Location	chr8:112439641-112697491
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	chr8:112576305-112577602	HepG2	liver:	n/a	n/a
2	ARID3A	chr8:112449828-112449990	HepG2	liver:	n/a	n/a
3	ARID3A	chr8:112456471-112456739	HepG2	liver:	n/a	n/a
4	BACH1	chr8:112565168-112565174	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr8:112691006-112691050	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr8:112692464-112692870	H1-hESC	embryonic stem cell:	n/a	n/a
7	BCL11A	chr8:112485985-112486203	H1-hESC	embryonic stem cell:	n/a	n/a
8	BHLHE40	chr8:112576576-112576903	HepG2	liver:	n/a	n/a
9	BRCA1	chr8:112691833-112692033	H1-hESC	embryonic stem cell:	n/a	n/a
10	CBX3	chr8:112678378-112678702	K562	blood:	n/a	n/a
11	CEBPB	chr8:112495005-112495321	IMR90	lung:	n/a	n/a
12	CEBPB	chr8:112578688-112578901	A549	lung:	n/a	chr8:112578719-112578732
13	CEBPB	chr8:112656669-112656973	A549	lung:	n/a	chr8:112656728-112656741 chr8:112656830-112656841
14	CEBPB	chr8:112589943-112590245	HepG2	liver:	n/a	chr8:112590133-112590146 chr8:112590111-112590122 chr8:112590110-112590123
15	CEBPB	chr8:112578664-112578920	HepG2	liver:	n/a	chr8:112578719-112578732
16	CEBPB	chr8:112603419-112603617	HepG2	liver:	n/a	chr8:112603525-112603536
17	CEBPB	chr8:112481791-112481991	H1-hESC	embryonic stem cell:	n/a	n/a
18	CEBPB	chr8:112618812-112619060	HepG2	liver:	n/a	chr8:112618953-112618964 chr8:112618955-112618964
19	CEBPB	chr8:112526364-112526721	HepG2	liver:	n/a	chr8:112526527-112526536 chr8:112526527-112526536 chr8:112526525-112526536 chr8:112526527-112526536 chr8:112526525-112526538 chr8:112526527-112526536 chr8:112526527-112526538
20	CEBPB	chr8:112526378-112526701	A549	lung:	n/a	chr8:112526527-112526536 chr8:112526527-112526536 chr8:112526525-112526536 chr8:112526527-112526536 chr8:112526525-112526538 chr8:112526527-112526536 chr8:112526527-112526538
21	CEBPB	chr8:112576445-112576921	HepG2	liver:	n/a	n/a
22	CEBPB	chr8:112519386-112519549	A549	lung:	n/a	n/a
23	CEBPB	chr8:112575228-112575538	HepG2	liver:	n/a	chr8:112575342-112575355 chr8:112575342-112575353 chr8:112575343-112575354 chr8:112575342-112575355
24	CEBPB	chr8:112631993-112632244	HepG2	liver:	n/a	chr8:112632167-112632180
25	CEBPB	chr8:112526372-112526696	K562	blood:	n/a	chr8:112526527-112526536 chr8:112526527-112526536 chr8:112526525-112526536 chr8:112526527-112526536 chr8:112526525-112526538 chr8:112526527-112526536 chr8:112526527-112526538
26	CEBPB	chr8:112589952-112590235	A549	lung:	n/a	chr8:112590133-112590146 chr8:112590111-112590122 chr8:112590110-112590123
27	CEBPB	chr8:112526420-112526708	ECC-1	luminal epithelium:	n/a	chr8:112526527-112526536 chr8:112526527-112526536 chr8:112526525-112526536 chr8:112526527-112526536 chr8:112526525-112526538 chr8:112526527-112526536 chr8:112526527-112526538
28	CEBPB	chr8:112603408-112603661	H1-hESC	embryonic stem cell:	n/a	chr8:112603525-112603536
29	CEBPB	chr8:112565892-112566140	HepG2	liver:	n/a	n/a
30	CEBPB	chr8:112576541-112576791	HepG2	liver:	n/a	n/a
31	CEBPB	chr8:112656695-112656966	IMR90	lung:	n/a	chr8:112656728-112656741 chr8:112656830-112656841
32	CEBPB	chr8:112648825-112649214	HepG2	liver:	n/a	chr8:112649115-112649126 chr8:112649115-112649126
33	CEBPB	chr8:112658465-112658728	MCF-7	breast:	n/a	n/a
34	CEBPB	chr8:112526367-112526717	IMR90	lung:	n/a	chr8:112526527-112526536 chr8:112526527-112526536 chr8:112526525-112526536 chr8:112526527-112526536 chr8:112526525-112526538 chr8:112526527-112526536 chr8:112526527-112526538
35	CEBPB	chr8:112481807-112482030	HepG2	liver:	n/a	n/a
36	CEBPB	chr8:112526403-112526670	H1-hESC	embryonic stem cell:	n/a	chr8:112526527-112526536 chr8:112526527-112526536 chr8:112526525-112526536 chr8:112526527-112526536 chr8:112526525-112526538 chr8:112526527-112526536 chr8:112526527-112526538
37	CEBPB	chr8:112656674-112657002	HepG2	liver:	n/a	chr8:112656728-112656741 chr8:112656830-112656841
38	CEBPZ	chr8:112496276-112496292	HepG2	liver:	n/a	n/a
39	CHD1	chr8:112693285-112693365	H1-hESC	embryonic stem cell:	n/a	n/a
40	CHD2	chr8:112691897-112692838	H1-hESC	embryonic stem cell:	n/a	n/a
41	CHD2	chr8:112576694-112576873	HepG2	liver:	n/a	n/a
42	CTBP2	chr8:112691896-112692704	H1-hESC	embryonic stem cell:	n/a	n/a
43	CTCF	chr8:112456560-112456710	AoAF	blood vessel:	n/a	chr8:112456624-112456645 chr8:112456622-112456640
44	CTCF	chr8:112456520-112456670	NHEK	skin:	n/a	chr8:112456624-112456645 chr8:112456622-112456640
45	CTCF	chr8:112456520-112456670	AG09319	gingival:	n/a	chr8:112456624-112456645 chr8:112456622-112456640
46	CTCF	chr8:112456540-112456690	Caco-2	colon:	n/a	chr8:112456624-112456645 chr8:112456622-112456640
47	CTCF	chr8:112456540-112456690	Hela-S3	cervix:	n/a	chr8:112456624-112456645 chr8:112456622-112456640
48	CTCF	chr8:112456471-112456801	H1-hESC	embryonic stem cell:	n/a	chr8:112456624-112456645 chr8:112456622-112456640
49	CTCF	chr8:112456417-112456711	HepG2	liver:	n/a	chr8:112456624-112456645 chr8:112456622-112456640
50	CTCF	chr8:112456540-112456690	HBMEC	blood vessel:	n/a	chr8:112456624-112456645 chr8:112456622-112456640

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:112482695-112482745	MCF10A-Er-Src	breast:	n/a
2	chr8:112482695-112482745	MCF10A-Er-Src	breast:	n/a
3	chr8:112482695-112482745	NHBE	bronchial:	n/a
4	chr8:112691450-112691500	HAEpiC	amniotic membrane:	n/a
5	chr8:112636625-112636675	CMK	blood:	n/a
6	chr8:112636613-112636663	RPTEC	kidney:	n/a
7	chr8:112636625-112636675	NH-A	brain:	n/a
8	chr8:112636613-112636663	HepG2	liver:	n/a
9	chr8:112482677-112482727	GM12892	blood:	n/a
10	chr8:112636613-112636663	T-47D	breast:	n/a
11	chr8:112636613-112636663	HCT-116	colon:	n/a
12	chr8:112636613-112636663	GM06990	blood:	n/a
13	chr8:112636625-112636675	Caco-2	colon:	n/a
14	chr8:112482677-112482727	IMR90	lung:	fetal
15	chr8:112691450-112691500	BE2_C	brain:	n/a
16	chr8:112636613-112636663	HCPEpiC	choroid plexus:	n/a
17	chr8:112636613-112636663	AG04450	lung:	fetal
18	chr8:112482695-112482745	NB4	blood:	n/a
19	chr8:112636625-112636675	HUVEC	blood vessel:	n/a
20	chr8:112655155-112655205	HCF	heart:	n/a
21	chr8:112691450-112691500	NHDF-neo	bronchial:	n/a
22	chr8:112612368-112612418	ovcar-3	ovarian:	n/a
23	chr8:112612368-112612418	NB4	blood:	n/a
24	chr8:112691450-112691500	GM12891	blood:	n/a
25	chr8:112655155-112655205	HCM	heart:	n/a
26	chr8:112482677-112482727	SK-N-SH	brain:	n/a
27	chr8:112691450-112691500	RPTEC	kidney:	n/a
28	chr8:112691450-112691500	AG09319	gingival:	n/a
29	chr8:112691450-112691500	HUVEC	blood vessel:	n/a
30	chr8:112655155-112655205	BJ	skin:	n/a
31	chr8:112482695-112482745	HMEC	breast:	n/a
32	chr8:112691450-112691500	LNCaP	prostate:	n/a
33	chr8:112612368-112612418	PANC-1	pancreas:	n/a
34	chr8:112655155-112655205	MCF10A-Er-Src	breast:	n/a
35	chr8:112691450-112691500	HRPEpiC	eye:	n/a
36	chr8:112691450-112691500	Caco-2	colon:	n/a
37	chr8:112636625-112636675	SK-N-SH_RA	brain:	n/a
38	chr8:112655155-112655205	HepG2	liver:	n/a
39	chr8:112691450-112691500	GM12892	blood:	n/a
40	chr8:112482695-112482745	Hela-S3	cervix:	n/a
41	chr8:112636613-112636663	AG04449	skin:	fetal
42	chr8:112612368-112612418	NHDF-neo	bronchial:	n/a
43	chr8:112612368-112612418	AG04449	skin:	fetal
44	chr8:112636625-112636675	AG09309	skin:	n/a
45	chr8:112482677-112482727	T-47D	breast:	n/a
46	chr8:112612368-112612418	AG04450	lung:	fetal
47	chr8:112655155-112655205	MCF-7	breast:	n/a
48	chr8:112636625-112636675	Jurkat	blood:	n/a
49	chr8:112612368-112612418	NHBE	bronchial:	n/a
50	chr8:112482695-112482745	A549	lung:	n/a

No.	Distal block	Cell Line	Cell type
1	chr8:112439221..112439930-chr8:112809136..112809948,2	MCF-7	breast:
2	chr8:112622384..112625093-chr8:112625173..112626907,2	MCF-7	breast:
3	chr8:112479743..112482044-chr8:112494341..112496246,2	K562	blood:
4	chr8:112456214..112456969-chr8:112758072..112758694,3	MCF-7	breast:
5	chr8:112622384..112625093-chr8:112625173..112626907,2	MCF-7	breast:
6	chr8:112458264..112460243-chr8:112464717..112466485,2	K562	blood:
7	chr8:112479743..112482044-chr8:112494341..112496246,2	K562	blood:
8	chr8:112438643..112439991-chr8:112809151..112809703,4	MCF-7	breast:
9	chr8:112561052..112562682-chr8:112563214..112564772,2	MCF-7	breast:
10	chr8:112561052..112562682-chr8:112563214..112564772,2	MCF-7	breast:
11	chr8:112466504..112469313-chr8:112470334..112472257,2	MCF-7	breast:
12	chr8:112455862..112457106-chr8:112809020..112809893,6	MCF-7	breast:
13	chr8:112466504..112469313-chr8:112470334..112472257,2	MCF-7	breast:
14	chr8:112456153..112457084-chr8:112809101..112810085,7	MCF-7	breast:
15	chr8:112458264..112460243-chr8:112464717..112466485,2	K562	blood:
16	chr8:112471086..112471839-chr8:112809518..112810102,2	MCF-7	breast:
17	chr8:112690809..112693633-chr8:112697668..112700424,2	K562	blood:
18	chr8:112570236..112571107-chr8:139584283..139585016,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RP11-422N16.3.1-4	chr8:112482610-112482846	ENSG00000253434.1
2	lnc-RP11-422N16.3.1-4	chr8:112555148-112555202	ENSG00000253434.1
3	lnc-RP11-422N16.3.1-4	chr8:112525276-112525364	ENSG00000253434.1
4	lnc-RP11-422N16.3.1-4	chr8:112554278-112554452	ENSG00000253434.1
5	lnc-RP11-422N16.3.1-4	chr8:112478407-112478529	ENSG00000253434.1
6	lnc-RP11-422N16.3.1-4	chr8:112527241-112527565	ENSG00000253434.1
7	lnc-RP11-422N16.3.1-4	chr8:112525276-112525364	ENSG00000253434.1
8	lnc-CSMD3-4	chr8:112633687-112634026	NONHSAT128329
9	lnc-RP11-422N16.3.1-4	chr8:112478407-112478529	ENSG00000253434.1
10	lnc-RP11-422N16.3.1-4	chr8:112478407-112478529	ENSG00000253434.1

Variant related genes	Relation type
ENSG00000253156	TF binding region
ENSG00000253156	CpG island

Extended variants
information (count: 2854 )
Associated
traits (count: 99 )

Variant overlapped rSNPs/rCNVs (count:2854 , 50 per page) page: 1 2 3 4 5 6 7 ... 58

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs116442403	chr8:112440858-112440859	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
2	rs551473357	chr8:112440892-112440893	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
3	rs73324268	chr8:112440910-112440911	Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs148514714	chr8:112440934-112440935	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
5	rs550606532	chr8:112441020-112441021	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
6	rs567550747	chr8:112441022-112441023	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
7	rs184369075	chr8:112441060-112441061	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
8	rs529762874	chr8:112441106-112441107	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
9	rs111930939	chr8:112441108-112441109	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
10	rs572609425	chr8:112441123-112441124	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
11	rs142819372	chr8:112441125-112441126	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
12	rs565862727	chr8:112441140-112441141	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
13	rs151027401	chr8:112441176-112441177	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
14	rs558196350	chr8:112441209-112441210	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
15	rs541122036	chr8:112441210-112441211	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
16	rs561358952	chr8:112441214-112441215	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
17	rs578115854	chr8:112441222-112441223	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
18	rs370640919	chr8:112441311-112441312	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
19	rs189470585	chr8:112441365-112441366	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
20	rs13254286	chr8:112441369-112441370	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
21	rs13254287	chr8:112441375-112441376	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
22	rs13252032	chr8:112441383-112441384	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
23	rs192498973	chr8:112441385-112441386	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
24	rs537604139	chr8:112441420-112441421	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
25	rs139775543	chr8:112441432-112441433	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
26	rs549793969	chr8:112441441-112441442	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
27	rs574378608	chr8:112441548-112441549	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
28	rs542678046	chr8:112441570-112441571	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
29	rs145271614	chr8:112441678-112441679	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
30	rs543786634	chr8:112441722-112441723	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
31	rs572842324	chr8:112441734-112441735	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
32	rs545136579	chr8:112441738-112441739	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
33	rs564949346	chr8:112441747-112441748	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
34	rs530665372	chr8:112441758-112441759	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
35	rs183929769	chr8:112441856-112441857	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
36	rs376149888	chr8:112441875-112441876	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
37	rs147627713	chr8:112441878-112441879	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
38	rs142161784	chr8:112441880-112441881	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
39	rs565749637	chr8:112441881-112441882	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
40	rs188207714	chr8:112441945-112441946	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
41	rs532664525	chr8:112441947-112441948	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
42	rs370273767	chr8:112441958-112441959	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
43	rs551585817	chr8:112441960-112441961	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
44	rs180770654	chr8:112441990-112441991	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
45	rs186623471	chr8:112441994-112441995	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
46	rs557513963	chr8:112441996-112441997	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
47	rs189415855	chr8:112442023-112442024	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
48	rs6981776	chr8:112442118-112442119	Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs553664235	chr8:112442140-112442141	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
50	rs572880892	chr8:112442150-112442151	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:99)

Disease	PMID	Source
Melanoma	18172304	CNVD
Medulloblastoma	21979893	CNVD
Ewing''s sarcoma	21437220	CNVD
Autism	19415332	CNVD
Malaria	21533027	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Esophageal cancer	21851588	CNVD
Gastric cancer	17908304	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Liver carcinoma	19366792	CNVD
Seminomas	18059402	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Pancreatic cancer	21811587	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	17603634	CNVD
Testicular cancer	18059402	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21509527	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Cancer	20164919	CNVD
abnormal development	18461090	CNVD
Oral cancer	21386901	CNVD
Uveal melanoma	21693616	CNVD
Langer-Giedion syndrome	22283845	CNVD
Cancer	21637783	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	20632083	CNVD
Breast cancer	19602461	CNVD
Cancer	22429812	CNVD
Endometrial cancer	22040021	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Hepatocellular carcinoma	22174799	CNVD
Oral cancer	19627613	CNVD
Prostate cancer	21088497	CNVD
colon cancer	17210682	CNVD
Breast cancer	21264507	CNVD
Breast cancer	22028636	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	16751803	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Gastric cancer	17167181	CNVD
Colorectal cancer	19359472	CNVD
Breast cancer	16461572	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	16968546	CNVD
head and neck squamous cell carcinoma	18028549	CNVD
Breast cancer	17001317	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ewing''s sarcoma	17952124	CNVD
Urothelial carcinoma	21177765	CNVD
Lung cancer	18438408	CNVD
Breast cancer	16608533	CNVD
Metanephric adenoma	20802469	CNVD
Hepatocellular carcinoma	18803288	CNVD
Prostate cancer	18632612	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	16573809	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Adenocarcinoma	21044232	CNVD
Squamous cell cancer	20885788	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	21399628	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Breast cancer	17393978	CNVD
Burkitt''s lymphoma	18698080	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Breast cancer	17899364	CNVD
Acute myeloid leukemia	21251322	CNVD
lymphocytic leukemia	21291569	CNVD
Colorectal cancer	16774939	CNVD
Autosomal-dominant progressive external ophthalmoplegia	19664747	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Sezary syndrome	18413736	CNVD
Breast cancer	21611746	CNVD
Developmental delay	21147756	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Congenital diaphragmatic hernia	21525063	CNVD
Non-small cell lung cancer	19010865	CNVD
small cell lung cancer	20016488	CNVD
Chronic myeloid leukemia	21384125	CNVD
Breast cancer	21364760	CNVD
Neuroticism	17667963	CNVD
Papillary thyroid cancer	17515504	CNVD
Basal cell lymphoma	17053054	CNVD
Bipolar disorder	19114987	CNVD
early-passage human iPS cells	21368824	CNVD
Renal cell carcinoma	21215367	CNVD

Chromatin state (count:167 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:112440800-112441000	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
2	chr8:112440800-112441800	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
3	chr8:112441400-112442000	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
4	chr8:112442000-112442200	Bivalent Enhancer	iPS DF 6.9 Cell Line	embryonic stem cell
5	chr8:112447400-112448800	Enhancers	iPS-15b Cell Line	embryonic stem cell
6	chr8:112447600-112448600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
7	chr8:112448200-112448800	Enhancers	iPS-18 Cell Line	embryonic stem cell
8	chr8:112448600-112465600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
9	chr8:112450200-112451200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
10	chr8:112455800-112456200	Enhancers	Fetal Brain Female	brain
11	chr8:112462600-112464200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
12	chr8:112463400-112464200	Enhancers	Brain Germinal Matrix	brain
13	chr8:112474600-112478600	Enhancers	HSMM	muscle
14	chr8:112475400-112475600	Enhancers	HSMMtube	muscle
15	chr8:112475400-112476400	Enhancers	Muscle Satellite Cultured Cells	--
16	chr8:112475600-112481000	Weak transcription	HSMMtube	muscle
17	chr8:112476400-112476800	Weak transcription	Muscle Satellite Cultured Cells	--
18	chr8:112476800-112478800	Enhancers	Muscle Satellite Cultured Cells	--
19	chr8:112478800-112480600	Weak transcription	Muscle Satellite Cultured Cells	--
20	chr8:112480600-112481600	Enhancers	Muscle Satellite Cultured Cells	--
21	chr8:112480600-112481800	Enhancers	Monocytes-CD14+_RO01746	blood
22	chr8:112480800-112482000	Enhancers	Primary neutrophils fromperipheralblood	blood
23	chr8:112481000-112481200	Enhancers	HSMMtube	muscle
24	chr8:112481400-112481800	Enhancers	Primary monocytes fromperipheralblood	blood
25	chr8:112482200-112482600	Weak transcription	Adipose Nuclei	Adipose
26	chr8:112482600-112484400	ZNF genes & repeats	Adipose Nuclei	Adipose
27	chr8:112482800-112483200	ZNF genes & repeats	Pancreas	Pancrea
28	chr8:112482800-112483600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
29	chr8:112482800-112483600	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
30	chr8:112482800-112483600	Active TSS	Spleen	Spleen
31	chr8:112483800-112486000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
32	chr8:112484400-112489000	Weak transcription	Adipose Nuclei	Adipose
33	chr8:112485600-112486200	Enhancers	HUES64 Cell Line	embryonic stem cell
34	chr8:112485600-112487800	Enhancers	iPS-15b Cell Line	embryonic stem cell
35	chr8:112485800-112487000	Enhancers	HUES6 Cell Line	embryonic stem cell
36	chr8:112486000-112486400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
37	chr8:112486000-112486600	Enhancers	iPS-20b Cell Line	embryonic stem cell
38	chr8:112486000-112486800	Enhancers	HUES48 Cell Line	embryonic stem cell
39	chr8:112486000-112487400	Enhancers	H1 Cell Line	embryonic stem cell
40	chr8:112486200-112486800	Enhancers	ES-I3 Cell Line	embryonic stem cell
41	chr8:112486200-112486800	Enhancers	H9 Cell Line	embryonic stem cell
42	chr8:112486800-112487800	Weak transcription	H9 Cell Line	embryonic stem cell
43	chr8:112487800-112488000	Enhancers	H9 Cell Line	embryonic stem cell
44	chr8:112489000-112489400	Enhancers	Adipose Nuclei	Adipose
45	chr8:112498200-112498600	Enhancers	Brain Inferior Temporal Lobe	brain
46	chr8:112498200-112499400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
47	chr8:112538600-112539000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
48	chr8:112539000-112544000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
49	chr8:112539200-112540000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
50	chr8:112544000-112544600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell

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