Variant report

Variant	nsv890834
Chromosome Location	chr8:39429071-39586358
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:358)
CpG islands
(count:429)
Chromatin interactive
region (count:8)
LncRNA
region (count:30)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:358 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:39547188-39547606	HepG2	liver:	n/a	n/a
2	ATF1	chr8:39574502-39574589	K562	blood:	n/a	n/a
3	ATF1	chr8:39552789-39552868	K562	blood:	n/a	n/a
4	ATF2	chr8:39542169-39542470	GM12878	blood:	n/a	n/a
5	BATF	chr8:39542225-39542523	GM12878	blood:	n/a	n/a
6	BATF	chr8:39542251-39542689	GM12878	blood:	n/a	n/a
7	BATF	chr8:39538369-39538590	GM12878	blood:	n/a	chr8:39538508-39538519
8	BCL11A	chr8:39542248-39542605	GM12878	blood:	n/a	n/a
9	BCL11A	chr8:39542183-39542620	GM12878	blood:	n/a	n/a
10	BCLAF1	chr8:39542279-39542596	GM12878	blood:	n/a	n/a
11	BHLHE40	chr8:39540522-39540568	GM12878	blood:	n/a	n/a
12	BHLHE40	chr8:39439456-39439600	K562	blood:	n/a	n/a
13	BHLHE40	chr8:39542060-39542776	GM12878	blood:	n/a	n/a
14	CBX3	chr8:39498734-39499015	HCT-116	colon:	n/a	n/a
15	CBX3	chr8:39436347-39436562	K562	blood:	n/a	n/a
16	CBX3	chr8:39471220-39471427	K562	blood:	n/a	n/a
17	CCNT2	chr8:39550530-39550861	K562	blood:	n/a	n/a
18	CEBPB	chr8:39458127-39458460	HepG2	liver:	n/a	chr8:39458289-39458300
19	CEBPB	chr8:39562615-39562959	IMR90	lung:	n/a	n/a
20	CEBPB	chr8:39550934-39551155	IMR90	lung:	n/a	chr8:39551018-39551029
21	CEBPB	chr8:39550893-39551144	K562	blood:	n/a	chr8:39551018-39551029
22	CEBPB	chr8:39562606-39562938	HepG2	liver:	n/a	n/a
23	CEBPB	chr8:39444289-39444489	IMR90	lung:	n/a	chr8:39444383-39444394 chr8:39444381-39444394
24	CEBPB	chr8:39444323-39444503	A549	lung:	n/a	chr8:39444383-39444394 chr8:39444381-39444394
25	CEBPB	chr8:39562647-39562945	A549	lung:	n/a	n/a
26	CEBPB	chr8:39458160-39458460	A549	lung:	n/a	chr8:39458289-39458300
27	CEBPB	chr8:39584624-39585155	H1-hESC	embryonic stem cell:	n/a	n/a
28	CEBPB	chr8:39536157-39536372	HepG2	liver:	n/a	chr8:39536260-39536272
29	CEBPB	chr8:39545791-39545917	A549	lung:	n/a	n/a
30	CEBPB	chr8:39562626-39562905	H1-hESC	embryonic stem cell:	n/a	n/a
31	CEBPB	chr8:39550875-39551134	HepG2	liver:	n/a	chr8:39551018-39551029
32	CHD1	chr8:39544449-39544453	GM12878	blood:	n/a	n/a
33	CHD1	chr8:39543635-39543758	GM12878	blood:	n/a	n/a
34	CHD1	chr8:39542597-39542843	GM12878	blood:	n/a	n/a
35	CHD2	chr8:39511704-39511832	K562	blood:	n/a	n/a
36	CHD2	chr8:39541932-39543050	GM12878	blood:	n/a	n/a
37	CHD2	chr8:39458585-39458752	K562	blood:	n/a	n/a
38	CTCF	chr8:39564300-39564450	BE2_C	brain:	n/a	n/a
39	CTCF	chr8:39530060-39530210	BE2_C	brain:	n/a	n/a
40	CTCF	chr8:39484841-39484900	GM20000	blood:	n/a	n/a
41	CTCF	chr8:39470080-39470230	HepG2	liver:	n/a	n/a
42	CTCF	chr8:39470040-39470190	GM12869	blood:	n/a	n/a
43	CTCF	chr8:39470040-39470190	A549	lung:	n/a	n/a
44	CTCF	chr8:39470020-39470170	GM12864	blood:	n/a	n/a
45	CTCF	chr8:39545941-39545950	GM10248	blood:	n/a	n/a
46	CTCF	chr8:39470000-39470150	GM12872	blood:	n/a	n/a
47	CTCF	chr8:39501960-39502110	GM12868	blood:	n/a	n/a
48	CTCF	chr8:39470060-39470210	GM12873	blood:	n/a	n/a
49	CTCF	chr8:39470060-39470210	GM12864	blood:	n/a	n/a
50	CTCF	chr8:39531405-39531462	GM13976	blood:	n/a	n/a

(count:429 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:39442347-39442397	GM06990	blood:	n/a
2	chr8:39441473-39441523	HL-60	blood:	n/a
3	chr8:39442347-39442397	GM06990	blood:	n/a
4	chr8:39441473-39441523	HL-60	blood:	n/a
5	chr8:39442347-39442397	HPAEpiC	pulmonary alveolar:	n/a
6	chr8:39441968-39442018	SK-N-MC	brain:	n/a
7	chr8:39442078-39442128	ProgFib	skin:	n/a
8	chr8:39441473-39441523	GM12878	blood:	n/a
9	chr8:39442089-39442139	SAEC	small airway:	n/a
10	chr8:39442089-39442139	Jurkat	blood:	n/a
11	chr8:39442347-39442397	HEEpiC	esophagus:	n/a
12	chr8:39442089-39442139	U87	brain:	n/a
13	chr8:39441968-39442018	Hepatocyte	liver:	n/a
14	chr8:39441473-39441523	HCM	heart:	n/a
15	chr8:39442080-39442130	PFSK-1	brain:	n/a
16	chr8:39441975-39442025	NHBE	bronchial:	n/a
17	chr8:39441473-39441523	HCT-116	colon:	n/a
18	chr8:39441975-39442025	GM12891	blood:	n/a
19	chr8:39442078-39442128	HEK293	kidney:	embryo
20	chr8:39442089-39442139	Hela-S3	cervix:	n/a
21	chr8:39441968-39442018	BJ	skin:	n/a
22	chr8:39441473-39441523	HAEpiC	amniotic membrane:	n/a
23	chr8:39441473-39441523	HPAEpiC	pulmonary alveolar:	n/a
24	chr8:39441975-39442025	PANC-1	pancreas:	n/a
25	chr8:39442347-39442397	ProgFib	skin:	n/a
26	chr8:39442080-39442130	NT2-D1	testis:	n/a
27	chr8:39442089-39442139	GM12891	blood:	n/a
28	chr8:39441975-39442025	AoSMC	blood vessel:	n/a
29	chr8:39441473-39441523	GM12892	blood:	n/a
30	chr8:39442347-39442397	MCF10A-Er-Src	breast:	n/a
31	chr8:39442347-39442397	ECC-1	luminal epithelium:	n/a
32	chr8:39442089-39442139	PANC-1	pancreas:	n/a
33	chr8:39441968-39442018	NB4	blood:	n/a
34	chr8:39442080-39442130	U87	brain:	n/a
35	chr8:39442078-39442128	HPAEpiC	pulmonary alveolar:	n/a
36	chr8:39442080-39442130	GM12878	blood:	n/a
37	chr8:39441968-39442018	HPAEpiC	pulmonary alveolar:	n/a
38	chr8:39441975-39442025	RPTEC	kidney:	n/a
39	chr8:39441968-39442018	AG09309	skin:	n/a
40	chr8:39441473-39441523	BE2_C	brain:	n/a
41	chr8:39442078-39442128	AG09319	gingival:	n/a
42	chr8:39442080-39442130	HRCEpiC	kidney:	n/a
43	chr8:39442089-39442139	PrEC	prostate:	n/a
44	chr8:39441975-39442025	HAEpiC	amniotic membrane:	n/a
45	chr8:39441968-39442018	GM12892	blood:	n/a
46	chr8:39441473-39441523	K562	blood:	n/a
47	chr8:39441473-39441523	GM12891	blood:	n/a
48	chr8:39442080-39442130	HNPCEpiC	eye:	n/a
49	chr8:39441975-39442025	HL-60	blood:	n/a
50	chr8:39441473-39441523	MCF10A-Er-Src	breast:	n/a

(count:8 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:39202201..39204201-chr8:39430573..39432669,2	K562	blood:
2	chr8:39502547..39504602-chr8:39509034..39511259,2	K562	blood:
3	chr8:39502547..39504602-chr8:39509034..39511259,2	K562	blood:
4	chr8:39578570..39581049-chr8:39586519..39588228,2	MCF-7	breast:
5	chr8:39454127..39456246-chr8:39457674..39459630,2	K562	blood:
6	chr8:39436752..39438273-chr8:39442880..39445329,2	MCF-7	breast:
7	chr8:39436752..39438273-chr8:39442880..39445329,2	MCF-7	breast:
8	chr8:39454127..39456246-chr8:39457674..39459630,2	K562	blood:

(count:30 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ADAM18-1	chr8:39430763-39430927	NONHSAT126174
2	lnc-IDO1-4	chr8:39468048-39468263	NONHSAT126178
3	lnc-IDO1-2	chr8:39549919-39550084	l_3583_chr8:39549918-39556807_testes
4	lnc-IDO1-3	chr8:39564309-39564423	NONHSAT126179
5	lnc-ADAM18-1	chr8:39437484-39437653	NONHSAT126175
6	lnc-IDO1-2	chr8:39556641-39556699	l_3583_chr8:39549918-39556807_testes
7	lnc-ADAM18-1	chr8:39435933-39435990	NONHSAT126175
8	lnc-ADAM18-1	chr8:39437484-39437653	ENSG00000254082
9	lnc-IDO1-3	chr8:39550119-39550199	NONHSAT126179
10	lnc-IDO1-4	chr8:39463826-39463881	NONHSAT126178
11	lnc-ADAM18-1	chr8:39437484-39437653	ENSG00000254082
12	lnc-IDO1-3	chr8:39542693-39542931	NONHSAT126180
13	lnc-IDO1-4	chr8:39467004-39467080	NONHSAT126178
14	lnc-ADAM18-1	chr8:39433113-39433157	ENSG00000254082
15	lnc-IDO1-3	chr8:39550119-39550199	NONHSAT126180
16	lnc-ADAM18-1	chr8:39435933-39435990	ENSG00000254082
17	lnc-ADAM18-1	chr8:39430763-39430927	ENSG00000254082
18	lnc-IDO1-4	chr8:39462146-39462255	NONHSAT126178
19	lnc-IDO1-3	chr8:39581267-39581477	NONHSAT126180
20	lnc-IDO1-4	chr8:39466561-39466639	NONHSAT126178
21	lnc-IDO1-3	chr8:39581267-39581426	NONHSAT126179
22	lnc-ADAM18-1	chr8:39437484-39437653	NONHSAT126174
23	lnc-ADAM18-1	chr8:39430763-39430927	NONHSAT126175
24	lnc-ADAM18-1	chr8:39433100-39433157	NONHSAT126174
25	lnc-IDO1-2	chr8:39556704-39556807	l_3583_chr8:39549918-39556807_testes
26	lnc-ADAM18-1	chr8:39433100-39433157	ENSG00000254082
27	lnc-ADAM18-1	chr8:39433100-39433160	NONHSAT126175
28	lnc-IDO1-3	chr8:39542649-39542931	NONHSAT126179
29	lnc-IDO1-2	chr8:39552257-39552314	l_3583_chr8:39549918-39556807_testes
30	lnc-IDO1-3	chr8:39564309-39564423	NONHSAT126180

No data

Variant related genes	Relation type
ADAM18	TF binding region
ENSG00000254082	TF binding region
ADAM18	CpG island
ENSG00000254082	CpG island

Extended variants
information (count: 3240 )
Associated
traits (count: 117 )

Variant overlapped rSNPs/rCNVs (count:3240 , 50 per page) page: 1 2 3 4 5 6 7 ... 65

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7830114	chr8:39429071-39429072	Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs537820379	chr8:39429171-39429172	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs6474158	chr8:39429219-39429220	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs139223693	chr8:39429225-39429226	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs528598082	chr8:39429306-39429307	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs191969842	chr8:39429331-39429332	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs370957497	chr8:39429338-39429339	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs79102524	chr8:39429350-39429351	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs546668098	chr8:39429415-39429416	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs373507465	chr8:39429416-39429417	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs76274533	chr8:39429427-39429428	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs375667824	chr8:39429480-39429481	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs574264235	chr8:39429512-39429513	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs149533056	chr8:39429552-39429553	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs538639844	chr8:39429574-39429575	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs9657180	chr8:39429581-39429582	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs73603927	chr8:39429597-39429598	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs564099582	chr8:39429630-39429631	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs62510549	chr8:39429658-39429659	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs546265455	chr8:39429685-39429686	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs145948789	chr8:39429769-39429770	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs529018834	chr8:39429871-39429872	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs536461664	chr8:39429908-39429909	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs184383138	chr8:39429924-39429925	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs112969867	chr8:39429929-39429930	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs538249971	chr8:39429938-39429939	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs551527572	chr8:39429946-39429947	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs36094519	chr8:39429982-39429983	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs574679021	chr8:39429993-39429994	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs534316947	chr8:39430028-39430029	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs189157762	chr8:39430047-39430048	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs367650626	chr8:39430059-39430060	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs139825638	chr8:39430060-39430061	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs536814645	chr8:39430116-39430117	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs143130700	chr8:39430208-39430209	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs57955982	chr8:39430254-39430255	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs146216443	chr8:39430357-39430358	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs181883673	chr8:39430358-39430359	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs148416915	chr8:39430378-39430379	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs9298569	chr8:39430415-39430416	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs62510559	chr8:39430435-39430436	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs539952681	chr8:39430436-39430437	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs559786607	chr8:39430466-39430467	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs140031664	chr8:39430558-39430559	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs529054678	chr8:39430569-39430570	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs78806414	chr8:39430599-39430600	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs7010313	chr8:39430627-39430628	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs74859251	chr8:39430676-39430677	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs201148670	chr8:39430679-39430680	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs551634133	chr8:39430750-39430751	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:117)

Disease	PMID	Source
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Medulloblastoma	21979893	CNVD
Prostate cancer	16573809	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
Hepatocellular carcinoma	22174799	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
Melanoma	18172304	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
Thoracic aortic aneurysm	21092924	CNVD
Acute myeloid leukemia	20729466	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Seminomas	18059402	CNVD
Lung cancer	18438408	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
Endometrioid adenocarcinoma	16974079	CNVD
Pancreatic cancer	21811587	CNVD
Multiple myeloma	16461302	CNVD
Developmental delay	21373258	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	17603634	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Disorders of sex development	21048976	CNVD
Testicular cancer	18059402	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Hepatocellular carcinoma	16750200	CNVD
Bladder cancer	19088036	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Breast cancer	17001308	CNVD
Breast cancer	17157792	CNVD
Cancer	17001308	CNVD
Cancer	18840272	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Chordoma	18071362	CNVD
Salivary gland tumor	18059337	CNVD
Breast cancer	17133270	CNVD
Breast cancer	16608533	CNVD
Breast cancer	21509527	CNVD
Breast cancer	21785460	CNVD
abnormal development	18461090	CNVD
Breast cancer	16620391	CNVD
Rhabdomyosarcoma	16790082	CNVD
Prostate cancer	18632612	CNVD
Glioblastoma multiforme	21138945	CNVD
Prader-willi syndrome	20588305	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21858162	CNVD
Cancer	20164920	CNVD
Breast cancer	20932292	CNVD
Schizophrenia	20967226	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
early-passage human iPS cells	21368824	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Glioma	20126413	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Medulloblastoma	21163964	CNVD
Cancer	21249187	CNVD
Autism	19287141	CNVD
Rett syndrome	21593744	CNVD
Recurrent pregnancy loss	19789632	CNVD
Cancer	21272361	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Bladder cancer	21909424	CNVD
Breast cancer	22522925	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:181 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:39426000-39434200	Weak transcription	Placenta	Placenta
2	chr8:39428000-39434000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr8:39434000-39434400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr8:39434000-39435800	Enhancers	Placenta Amnion	Placenta Amnion
5	chr8:39434200-39434800	Enhancers	Placenta	Placenta
6	chr8:39434400-39435600	Enhancers	iPS-15b Cell Line	embryonic stem cell
7	chr8:39434400-39437800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
8	chr8:39434600-39435800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
9	chr8:39434800-39435200	Enhancers	iPS-20b Cell Line	embryonic stem cell
10	chr8:39434800-39435400	Weak transcription	Placenta	Placenta
11	chr8:39435000-39435600	Enhancers	HUES64 Cell Line	embryonic stem cell
12	chr8:39435200-39435400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
13	chr8:39435200-39435400	Enhancers	HepG2	liver
14	chr8:39435400-39436200	Weak transcription	HepG2	liver
15	chr8:39435400-39436400	Enhancers	Placenta	Placenta
16	chr8:39435400-39438200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
17	chr8:39435600-39436400	Enhancers	Primary hematopoietic stem cells	blood
18	chr8:39435800-39436800	Weak transcription	Placenta Amnion	Placenta Amnion
19	chr8:39436200-39437000	Enhancers	HepG2	liver
20	chr8:39436400-39437600	Weak transcription	Placenta	Placenta
21	chr8:39436800-39438200	Enhancers	Fetal Heart	heart
22	chr8:39436800-39438200	Enhancers	Placenta Amnion	Placenta Amnion
23	chr8:39437000-39438400	Weak transcription	HepG2	liver
24	chr8:39437000-39439200	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
25	chr8:39437600-39439600	Enhancers	Placenta	Placenta
26	chr8:39437800-39439000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
27	chr8:39438200-39438600	ZNF genes & repeats	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
28	chr8:39438200-39438600	Active TSS	Fetal Heart	heart
29	chr8:39438200-39439000	Weak transcription	Placenta Amnion	Placenta Amnion
30	chr8:39438600-39439200	Flanking Active TSS	Fetal Heart	heart
31	chr8:39438600-39439400	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
32	chr8:39438800-39439200	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
33	chr8:39438800-39440800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
34	chr8:39439000-39439200	Enhancers	Placenta Amnion	Placenta Amnion
35	chr8:39439000-39440200	Enhancers	Fetal Intestine Large	intestine
36	chr8:39439000-39442000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
37	chr8:39439200-39439400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
38	chr8:39439200-39439400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
39	chr8:39439200-39439800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
40	chr8:39439200-39439800	Weak transcription	Placenta Amnion	Placenta Amnion
41	chr8:39439200-39440800	Enhancers	Fetal Intestine Small	intestine
42	chr8:39439200-39441200	Enhancers	Fetal Heart	heart
43	chr8:39439400-39439600	Enhancers	ES-I3 Cell Line	embryonic stem cell
44	chr8:39439400-39439600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
45	chr8:39439400-39439600	Enhancers	HepG2	liver
46	chr8:39439400-39439800	Enhancers	Cortex derived primary cultured neurospheres	brain
47	chr8:39439400-39440600	Weak transcription	HUES6 Cell Line	embryonic stem cell
48	chr8:39439600-39440000	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
49	chr8:39439800-39440000	Enhancers	Placenta Amnion	Placenta Amnion
50	chr8:39440000-39440200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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