Variant report

Variant	nsv891314
Chromosome Location	chr8:112463865-112649830
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	BACH1	chr8:112565168-112565174	H1-hESC	embryonic stem cell:	n/a	n/a
3	BCL11A	chr8:112485985-112486203	H1-hESC	embryonic stem cell:	n/a	n/a
4	BHLHE40	chr8:112576576-112576903	HepG2	liver:	n/a	n/a
5	CEBPB	chr8:112565892-112566140	HepG2	liver:	n/a	n/a
6	CEBPB	chr8:112575228-112575538	HepG2	liver:	n/a	chr8:112575342-112575355 chr8:112575342-112575353 chr8:112575343-112575354 chr8:112575342-112575355
7	CEBPB	chr8:112578664-112578920	HepG2	liver:	n/a	chr8:112578719-112578732
8	CEBPB	chr8:112603419-112603617	HepG2	liver:	n/a	chr8:112603525-112603536
9	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
10	CEBPB	chr8:112631993-112632244	HepG2	liver:	n/a	chr8:112632167-112632180
11	CEBPB	chr8:112519386-112519549	A549	lung:	n/a	n/a
12	CEBPB	chr8:112603408-112603661	H1-hESC	embryonic stem cell:	n/a	chr8:112603525-112603536
13	CEBPB	chr8:112578688-112578901	A549	lung:	n/a	chr8:112578719-112578732
14	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
15	CEBPB	chr8:112648825-112649214	HepG2	liver:	n/a	chr8:112649115-112649126 chr8:112649115-112649126
16	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
17	CEBPB	chr8:112481807-112482030	HepG2	liver:	n/a	n/a
18	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
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	chr8:112576445-112576921	HepG2	liver:	n/a	n/a
21	CEBPB	chr8:112495005-112495321	IMR90	lung:	n/a	n/a
22	CEBPB	chr8:112589952-112590235	A549	lung:	n/a	chr8:112590133-112590146 chr8:112590111-112590122 chr8:112590110-112590123
23	CEBPB	chr8:112481791-112481991	H1-hESC	embryonic stem cell:	n/a	n/a
24	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
25	CEBPB	chr8:112576541-112576791	HepG2	liver:	n/a	n/a
26	CEBPB	chr8:112589943-112590245	HepG2	liver:	n/a	chr8:112590133-112590146 chr8:112590111-112590122 chr8:112590110-112590123
27	CEBPB	chr8:112618812-112619060	HepG2	liver:	n/a	chr8:112618953-112618964 chr8:112618955-112618964
28	CEBPZ	chr8:112496276-112496292	HepG2	liver:	n/a	n/a
29	CHD2	chr8:112576694-112576873	HepG2	liver:	n/a	n/a
30	CTCF	chr8:112497343-112497458	GM10248	blood:	n/a	n/a
31	CTCF	chr8:112636205-112636329	HepG2	liver:	n/a	n/a
32	CTCF	chr8:112637136-112637227	HepG2	liver:	n/a	n/a
33	CTCF	chr8:112636237-112636326	MCF-7	breast:	n/a	n/a
34	CTCF	chr8:112636198-112636256	MCF-7	breast:	n/a	n/a
35	CTCF	chr8:112483000-112483150	GM12871	blood:	n/a	n/a
36	CTCF	chr8:112625382-112625439	Pancreas_OC	pancreas:	n/a	n/a
37	CTCF	chr8:112637080-112637230	HepG2	liver:	n/a	n/a
38	CTCF	chr8:112637100-112637250	WERI-Rb-1	eye:	n/a	n/a
39	CTCF	chr8:112637040-112637190	HEK293	kidney:	n/a	n/a
40	CTCF	chr8:112637016-112637365	H1-hESC	embryonic stem cell:	n/a	n/a
41	CTCF	chr8:112637220-112637370	MCF-7	breast:	n/a	n/a
42	CTCF	chr8:112601706-112601740	GM13976	blood:	n/a	n/a
43	CTCF	chr8:112636180-112636330	MCF-7	breast:	n/a	n/a
44	CTCF	chr8:112528536-112528572	GM10248	blood:	n/a	n/a
45	CTCF	chr8:112520760-112520910	HepG2	liver:	n/a	n/a
46	CTCF	chr8:112636215-112636372	HepG2	liver:	n/a	n/a
47	CTCF	chr8:112544120-112544270	HepG2	liver:	n/a	n/a
48	CTCF	chr8:112497342-112497458	Kidney_OC	kidney:	n/a	n/a
49	CTCF	chr8:112636220-112636370	MCF-7	breast:	n/a	n/a
50	CTCF	chr8:112636240-112636390	HepG2	liver:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:112636613-112636663	BJ	skin:	n/a
2	chr8:112636625-112636675	LNCaP	prostate:	n/a
3	chr8:112612368-112612418	HCF	heart:	n/a
4	chr8:112636613-112636663	AG10803	skin:	n/a
5	chr8:112612368-112612418	HUVEC	blood vessel:	n/a
6	chr8:112482695-112482745	IMR90	lung:	fetal
7	chr8:112636613-112636663	GM19239	blood:	n/a
8	chr8:112482677-112482727	SK-N-SH	brain:	n/a
9	chr8:112636613-112636663	HL-60	blood:	n/a
10	chr8:112636613-112636663	IMR90	lung:	fetal
11	chr8:112482695-112482745	HCM	heart:	n/a
12	chr8:112482695-112482745	BJ	skin:	n/a
13	chr8:112636625-112636675	HUVEC	blood vessel:	n/a
14	chr8:112612368-112612418	GM12892	blood:	n/a
15	chr8:112636613-112636663	HAEpiC	amniotic membrane:	n/a
16	chr8:112636625-112636675	AG10803	skin:	n/a
17	chr8:112636613-112636663	HCM	heart:	n/a
18	chr8:112636613-112636663	AG04450	lung:	fetal
19	chr8:112636613-112636663	ECC-1	luminal epithelium:	n/a
20	chr8:112612368-112612418	HepG2	liver:	n/a
21	chr8:112636625-112636675	Hepatocyte	liver:	n/a
22	chr8:112482677-112482727	SK-N-MC	brain:	n/a
23	chr8:112636625-112636675	MCF-7	breast:	n/a
24	chr8:112482677-112482727	HIPEpiC	eye:	n/a
25	chr8:112636613-112636663	HPAEpiC	pulmonary alveolar:	n/a
26	chr8:112482695-112482745	AoSMC	blood vessel:	n/a
27	chr8:112612368-112612418	SK-N-SH	brain:	n/a
28	chr8:112482677-112482727	MCF10A-Er-Src	breast:	n/a
29	chr8:112612368-112612418	HPAEpiC	pulmonary alveolar:	n/a
30	chr8:112636613-112636663	GM12878	blood:	n/a
31	chr8:112482677-112482727	NHBE	bronchial:	n/a
32	chr8:112482677-112482727	ECC-1	luminal epithelium:	n/a
33	chr8:112482695-112482745	AG04450	lung:	fetal
34	chr8:112636613-112636663	MCF-7	breast:	n/a
35	chr8:112612368-112612418	HNPCEpiC	eye:	n/a
36	chr8:112636613-112636663	HCPEpiC	choroid plexus:	n/a
37	chr8:112482695-112482745	PANC-1	pancreas:	n/a
38	chr8:112636613-112636663	RPTEC	kidney:	n/a
39	chr8:112612368-112612418	MCF-7	breast:	n/a
40	chr8:112636625-112636675	SAEC	small airway:	n/a
41	chr8:112482677-112482727	HMEC	breast:	n/a
42	chr8:112482677-112482727	HUVEC	blood vessel:	n/a
43	chr8:112482677-112482727	HEEpiC	esophagus:	n/a
44	chr8:112482695-112482745	HCT-116	colon:	n/a
45	chr8:112482677-112482727	BE2_C	brain:	n/a
46	chr8:112482695-112482745	AG04449	skin:	fetal
47	chr8:112482677-112482727	PrEC	prostate:	n/a
48	chr8:112612368-112612418	ProgFib	skin:	n/a
49	chr8:112612368-112612418	H1-hESC	embryonic stem cell:	embryo
50	chr8:112612368-112612418	T-47D	breast:	n/a

No.	Distal block	Cell Line	Cell type
1	chr8:112458264..112460243-chr8:112464717..112466485,2	K562	blood:
2	chr8:112622384..112625093-chr8:112625173..112626907,2	MCF-7	breast:
3	chr8:112561052..112562682-chr8:112563214..112564772,2	MCF-7	breast:
4	chr8:112479743..112482044-chr8:112494341..112496246,2	K562	blood:
5	chr8:112466504..112469313-chr8:112470334..112472257,2	MCF-7	breast:
6	chr8:112570236..112571107-chr8:139584283..139585016,2	MCF-7	breast:
7	chr8:112479743..112482044-chr8:112494341..112496246,2	K562	blood:
8	chr8:112471086..112471839-chr8:112809518..112810102,2	MCF-7	breast:
9	chr8:112561052..112562682-chr8:112563214..112564772,2	MCF-7	breast:
10	chr8:112622384..112625093-chr8:112625173..112626907,2	MCF-7	breast:
11	chr8:112466504..112469313-chr8:112470334..112472257,2	MCF-7	breast:

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

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

Extended variants
information (count: 1892 )
Associated
traits (count: 99 )

Variant overlapped rSNPs/rCNVs (count:1892 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1366852	chr8:112463865-112463866	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs548354032	chr8:112463885-112463886	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs538035872	chr8:112463894-112463895	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs188004087	chr8:112463903-112463904	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs57275126	chr8:112463932-112463933	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs560880948	chr8:112463962-112463963	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs144872777	chr8:112463978-112463979	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs1835175	chr8:112463980-112463981	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs539180588	chr8:112463995-112463996	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs191412875	chr8:112464001-112464002	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs552107452	chr8:112464027-112464028	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs138706852	chr8:112464036-112464037	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs183603487	chr8:112464047-112464048	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs141721442	chr8:112464067-112464068	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs144533321	chr8:112464084-112464085	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs540483225	chr8:112464098-112464099	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs549181718	chr8:112464123-112464124	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs562888243	chr8:112464143-112464144	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs187471545	chr8:112464155-112464156	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs192607906	chr8:112464192-112464193	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs141661270	chr8:112464210-112464211	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs184996021	chr8:112464233-112464234	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs548389726	chr8:112464234-112464235	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs568130497	chr8:112464342-112464343	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs534091904	chr8:112464344-112464345	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs547671111	chr8:112464375-112464376	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs566910143	chr8:112464406-112464407	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs539017213	chr8:112464423-112464424	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs558809061	chr8:112464462-112464463	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs569353108	chr8:112464507-112464508	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs537918304	chr8:112464545-112464546	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs555154441	chr8:112464636-112464637	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs567015024	chr8:112464669-112464670	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs540572884	chr8:112464682-112464683	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs554036676	chr8:112464695-112464696	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs568209237	chr8:112464776-112464777	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs150510908	chr8:112464790-112464791	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs531774735	chr8:112464831-112464832	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs562318918	chr8:112464868-112464869	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs28766119	chr8:112464884-112464885	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs551777608	chr8:112464960-112464961	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs531453463	chr8:112464990-112464991	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs377317582	chr8:112464995-112464996	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs541521868	chr8:112465005-112465006	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs187748112	chr8:112465094-112465095	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs6992235	chr8:112465119-112465120	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs547746162	chr8:112465148-112465149	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs570734786	chr8:112465182-112465183	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs192359715	chr8:112465192-112465193	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs1118214	chr8:112465210-112465211	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	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:69 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:112448600-112465600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr8:112462600-112464200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr8:112463400-112464200	Enhancers	Brain Germinal Matrix	brain
4	chr8:112474600-112478600	Enhancers	HSMM	muscle
5	chr8:112475400-112475600	Enhancers	HSMMtube	muscle
6	chr8:112475400-112476400	Enhancers	Muscle Satellite Cultured Cells	--
7	chr8:112475600-112481000	Weak transcription	HSMMtube	muscle
8	chr8:112476400-112476800	Weak transcription	Muscle Satellite Cultured Cells	--
9	chr8:112476800-112478800	Enhancers	Muscle Satellite Cultured Cells	--
10	chr8:112478800-112480600	Weak transcription	Muscle Satellite Cultured Cells	--
11	chr8:112480600-112481600	Enhancers	Muscle Satellite Cultured Cells	--
12	chr8:112480600-112481800	Enhancers	Monocytes-CD14+_RO01746	blood
13	chr8:112480800-112482000	Enhancers	Primary neutrophils fromperipheralblood	blood
14	chr8:112481000-112481200	Enhancers	HSMMtube	muscle
15	chr8:112481400-112481800	Enhancers	Primary monocytes fromperipheralblood	blood
16	chr8:112482200-112482600	Weak transcription	Adipose Nuclei	Adipose
17	chr8:112482600-112484400	ZNF genes & repeats	Adipose Nuclei	Adipose
18	chr8:112482800-112483200	ZNF genes & repeats	Pancreas	Pancrea
19	chr8:112482800-112483600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
20	chr8:112482800-112483600	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
21	chr8:112482800-112483600	Active TSS	Spleen	Spleen
22	chr8:112483800-112486000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
23	chr8:112484400-112489000	Weak transcription	Adipose Nuclei	Adipose
24	chr8:112485600-112486200	Enhancers	HUES64 Cell Line	embryonic stem cell
25	chr8:112485600-112487800	Enhancers	iPS-15b Cell Line	embryonic stem cell
26	chr8:112485800-112487000	Enhancers	HUES6 Cell Line	embryonic stem cell
27	chr8:112486000-112486400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
28	chr8:112486000-112486600	Enhancers	iPS-20b Cell Line	embryonic stem cell
29	chr8:112486000-112486800	Enhancers	HUES48 Cell Line	embryonic stem cell
30	chr8:112486000-112487400	Enhancers	H1 Cell Line	embryonic stem cell
31	chr8:112486200-112486800	Enhancers	ES-I3 Cell Line	embryonic stem cell
32	chr8:112486200-112486800	Enhancers	H9 Cell Line	embryonic stem cell
33	chr8:112486800-112487800	Weak transcription	H9 Cell Line	embryonic stem cell
34	chr8:112487800-112488000	Enhancers	H9 Cell Line	embryonic stem cell
35	chr8:112489000-112489400	Enhancers	Adipose Nuclei	Adipose
36	chr8:112498200-112498600	Enhancers	Brain Inferior Temporal Lobe	brain
37	chr8:112498200-112499400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
38	chr8:112538600-112539000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
39	chr8:112539000-112544000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
40	chr8:112539200-112540000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
41	chr8:112544000-112544600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
42	chr8:112551400-112552000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
43	chr8:112552800-112557800	Weak transcription	Adipose Nuclei	Adipose
44	chr8:112557200-112558800	Enhancers	Fetal Lung	lung
45	chr8:112557800-112558400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
46	chr8:112557800-112558600	Strong transcription	Adipose Nuclei	Adipose
47	chr8:112558600-112560200	Weak transcription	Adipose Nuclei	Adipose
48	chr8:112575200-112577600	Enhancers	Liver	Liver
49	chr8:112575800-112578400	Enhancers	HepG2	liver
50	chr8:112578200-112578400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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