Variant report

Variant	esv3324923
Chromosome Location	chr8:110370872-110377960
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	chr8:110377303-110377464	K562	blood:	n/a	n/a
2	ATF3	chr8:110374993-110375321	K562	blood:	n/a	n/a
3	BACH1	chr8:110374153-110374307	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr8:110374595-110374769	H1-hESC	embryonic stem cell:	n/a	n/a
5	BHLHE40	chr8:110374962-110375367	K562	blood:	n/a	n/a
6	CCNT2	chr8:110375105-110375623	K562	blood:	n/a	n/a
7	CEBPB	chr8:110374973-110375321	HepG2	liver:	n/a	chr8:110375144-110375157 chr8:110375145-110375156
8	CEBPB	chr8:110374978-110375480	K562	blood:	n/a	chr8:110375144-110375157 chr8:110375145-110375156
9	CEBPB	chr8:110374963-110375338	K562	blood:	n/a	chr8:110375144-110375157 chr8:110375145-110375156
10	CEBPD	chr8:110375104-110375574	K562	blood:	n/a	n/a
11	CEBPD	chr8:110375098-110375677	K562	blood:	n/a	n/a
12	CHD2	chr8:110374375-110374590	H1-hESC	embryonic stem cell:	n/a	n/a
13	CHD2	chr8:110374559-110374681	HepG2	liver:	n/a	n/a
14	CTBP2	chr8:110374005-110375078	H1-hESC	embryonic stem cell:	n/a	n/a
15	CTCF	chr8:110374649-110374682	Lung_OC	lung:	n/a	n/a
16	CTCF	chr8:110374600-110374750	Caco-2	colon:	n/a	chr8:110374672-110374685 chr8:110374669-110374687
17	CTCF	chr8:110374620-110374770	HBMEC	blood vessel:	n/a	chr8:110374672-110374685 chr8:110374669-110374687
18	CTCF	chr8:110374622-110374689	H1-hESC	embryonic stem cell:	n/a	chr8:110374672-110374685 chr8:110374669-110374687
19	CTCF	chr8:110374644-110374735	Pancreas_OC	pancreas:	n/a	chr8:110374672-110374685 chr8:110374669-110374687
20	CTCF	chr8:110374560-110374710	HRPEpiC	eye:	n/a	chr8:110374672-110374685 chr8:110374669-110374687
21	CTCF	chr8:110374639-110374709	MCF-7	breast:	n/a	chr8:110374672-110374685 chr8:110374669-110374687
22	CTCF	chr8:110374520-110374670	BJ	skin:	n/a	n/a
23	CTCF	chr8:110372273-110372326	MCF-7	breast:	n/a	n/a
24	CTCF	chr8:110374520-110374670	HRE	kidney:	n/a	n/a
25	CTCF	chr8:110374600-110374750	HA-sp	spinal cord:	n/a	chr8:110374672-110374685 chr8:110374669-110374687
26	CTCF	chr8:110374695-110374697	H1-hESC	embryonic stem cell:	n/a	n/a
27	CTCF	chr8:110374540-110374690	HRPEpiC	eye:	n/a	chr8:110374672-110374685 chr8:110374669-110374687
28	CTCF	chr8:110374655-110374699	MCF-7	breast:	n/a	chr8:110374672-110374685 chr8:110374669-110374687
29	CTCF	chr8:110374560-110374710	RPTEC	kidney:	n/a	chr8:110374672-110374685 chr8:110374669-110374687
30	CTCF	chr8:110374560-110374710	SAEC	small airway:	n/a	chr8:110374672-110374685 chr8:110374669-110374687
31	CTCF	chr8:110374440-110374590	Caco-2	colon:	n/a	n/a
32	CTCF	chr8:110374560-110374710	HA-sp	spinal cord:	n/a	chr8:110374672-110374685 chr8:110374669-110374687
33	CTCF	chr8:110374520-110374770	HUVEC	blood vessel:	n/a	chr8:110374672-110374685 chr8:110374669-110374687
34	CTCF	chr8:110374640-110374790	HRE	kidney:	n/a	chr8:110374672-110374685 chr8:110374669-110374687
35	CTCF	chr8:110374540-110374690	SAEC	small airway:	n/a	chr8:110374672-110374685 chr8:110374669-110374687
36	CTCF	chr8:110374620-110374770	AG09309	skin:	n/a	chr8:110374672-110374685 chr8:110374669-110374687
37	CTCF	chr8:110374580-110374730	HUVEC	blood vessel:	n/a	chr8:110374672-110374685 chr8:110374669-110374687
38	CTCF	chr8:110374586-110374768	MCF-7	breast:	n/a	chr8:110374672-110374685 chr8:110374669-110374687
39	CTCF	chr8:110374613-110374746	MCF-7	breast:	n/a	chr8:110374672-110374685 chr8:110374669-110374687
40	CTCF	chr8:110374560-110374710	WERI-Rb-1	eye:	n/a	chr8:110374672-110374685 chr8:110374669-110374687
41	CTCF	chr8:110374578-110374760	MCF-7	breast:	n/a	chr8:110374672-110374685 chr8:110374669-110374687
42	CTCF	chr8:110372264-110372286	K562	blood:	n/a	n/a
43	CTCF	chr8:110374580-110374730	WERI-Rb-1	eye:	n/a	chr8:110374672-110374685 chr8:110374669-110374687
44	CUX1	chr8:110375037-110375618	K562	blood:	n/a	n/a
45	CUX1	chr8:110376095-110376438	K562	blood:	n/a	n/a
46	EGR1	chr8:110372687-110372922	K562	blood:	n/a	chr8:110372836-110372847
47	EP300	chr8:110375905-110375971	K562	blood:	n/a	n/a
48	EP300	chr8:110372714-110372849	K562	blood:	n/a	n/a
49	EP300	chr8:110375081-110375638	K562	blood:	n/a	chr8:110375142-110375156
50	FOS	chr8:110371390-110371655	MCF10A-Er-Src	breast:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:110374374-110374424	ProgFib	skin:	n/a
2	chr8:110374675-110374725	AG04450	lung:	fetal
3	chr8:110374583-110374633	LNCaP	prostate:	n/a
4	chr8:110373460-110373510	SAEC	small airway:	n/a
5	chr8:110373460-110373510	GM12878	blood:	n/a
6	chr8:110374294-110374344	SK-N-SH_RA	brain:	n/a
7	chr8:110374374-110374424	HepG2	liver:	n/a
8	chr8:110374294-110374344	AG04450	lung:	fetal
9	chr8:110374585-110374635	GM19239	blood:	n/a
10	chr8:110374792-110374842	ovcar-3	ovarian:	n/a
11	chr8:110374583-110374633	HMEC	breast:	n/a
12	chr8:110374675-110374725	NH-A	brain:	n/a
13	chr8:110374294-110374344	NH-A	brain:	n/a
14	chr8:110373460-110373510	ECC-1	luminal epithelium:	n/a
15	chr8:110374563-110374613	GM19239	blood:	n/a
16	chr8:110373460-110373510	AG10803	skin:	n/a
17	chr8:110374866-110374916	NHBE	bronchial:	n/a
18	chr8:110374792-110374842	SK-N-SH_RA	brain:	n/a
19	chr8:110374585-110374635	HPAEpiC	pulmonary alveolar:	n/a
20	chr8:110373460-110373510	U87	brain:	n/a
21	chr8:110374374-110374424	Jurkat	blood:	n/a
22	chr8:110374792-110374842	PANC-1	pancreas:	n/a
23	chr8:110374294-110374344	Jurkat	blood:	n/a
24	chr8:110374563-110374613	HIPEpiC	eye:	n/a
25	chr8:110374585-110374635	HRE	kidney:	n/a
26	chr8:110374583-110374633	NT2-D1	testis:	n/a
27	chr8:110374294-110374344	T-47D	breast:	n/a
28	chr8:110374294-110374344	HEEpiC	esophagus:	n/a
29	chr8:110374563-110374613	HPAEpiC	pulmonary alveolar:	n/a
30	chr8:110374792-110374842	H1-hESC	embryonic stem cell:	embryo
31	chr8:110374792-110374842	K562	blood:	n/a
32	chr8:110374563-110374613	AG10803	skin:	n/a
33	chr8:110374585-110374635	GM06990	blood:	n/a
34	chr8:110374866-110374916	HEEpiC	esophagus:	n/a
35	chr8:110374585-110374635	HRCEpiC	kidney:	n/a
36	chr8:110374563-110374613	NHBE	bronchial:	n/a
37	chr8:110374563-110374613	NB4	blood:	n/a
38	chr8:110374792-110374842	ECC-1	luminal epithelium:	n/a
39	chr8:110374563-110374613	HCM	heart:	n/a
40	chr8:110374675-110374725	HEEpiC	esophagus:	n/a
41	chr8:110374585-110374635	ProgFib	skin:	n/a
42	chr8:110373460-110373510	HEEpiC	esophagus:	n/a
43	chr8:110374675-110374725	GM06990	blood:	n/a
44	chr8:110374563-110374613	Caco-2	colon:	n/a
45	chr8:110374585-110374635	SAEC	small airway:	n/a
46	chr8:110373460-110373510	HPAEpiC	pulmonary alveolar:	n/a
47	chr8:110374294-110374344	GM06990	blood:	n/a
48	chr8:110374792-110374842	SAEC	small airway:	n/a
49	chr8:110374563-110374613	GM12891	blood:	n/a
50	chr8:110374294-110374344	GM12892	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr8:110372108..110374370-chr8:110379678..110381794,2	K562	blood:
2	chr8:110369620..110372095-chr8:110373747..110377477,3	K562	blood:
3	chr8:110376237..110378577-chr8:110400092..110402254,2	K562	blood:
4	chr8:110373158..110374661-chr8:110392938..110394946,2	MCF-7	breast:
5	chr8:110365000..110368622-chr8:110368906..110372128,4	K562	blood:
6	chr8:110374980..110376608-chr8:110402670..110404308,2	K562	blood:
7	chr8:110375572..110377365-chr8:110452939..110455019,2	MCF-7	breast:
8	chr8:110371146..110373102-chr8:110382024..110383577,2	K562	blood:
9	chr8:110371418..110373000-chr8:110550789..110552367,2	K562	blood:
10	chr8:110367088..110368622-chr8:110370242..110371743,2	K562	blood:

Variant related genes	Relation type
PKHD1L1	TF binding region
PKHD1L1	CpG island
ENSG00000205038	chromatin interactions
ENSG00000147654	chromatin interactions

Extended variants
information (count: 244 )
Associated
traits (count: 101 )

Variant overlapped rSNPs/rCNVs (count:244 , 50 per page) page: 1 2 3 4 5

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs571512785	chr8:110370878-110370879	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs147052022	chr8:110370887-110370888	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs182553111	chr8:110370915-110370916	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs557251080	chr8:110370945-110370946	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs138406009	chr8:110371060-110371061	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs77991666	chr8:110371066-110371067	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs552948991	chr8:110371116-110371117	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs572839468	chr8:110371165-110371166	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs545119351	chr8:110371198-110371199	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs565136349	chr8:110371248-110371249	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs187335670	chr8:110371353-110371354	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs544403024	chr8:110371356-110371357	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs143806421	chr8:110371358-110371359	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs192219196	chr8:110371359-110371360	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs540245584	chr8:110371364-110371365	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs146427410	chr8:110371374-110371375	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs532496971	chr8:110371375-110371376	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs185501843	chr8:110371382-110371383	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs367858514	chr8:110371385-110371386	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs371254223	chr8:110371386-110371387	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs397700014	chr8:110371395-110371396	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs190500715	chr8:110371417-110371418	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs35629125	chr8:110371433-110371434	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs7835131	chr8:110371435-110371436	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
25	rs112875423	chr8:110371439-110371440	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs35890138	chr8:110371443-110371444	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs34980434	chr8:110371454-110371455	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs550817139	chr8:110371467-110371468	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs555517095	chr8:110371581-110371582	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs535864145	chr8:110371601-110371602	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs536583998	chr8:110371606-110371607	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs116397780	chr8:110371625-110371626	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs566511016	chr8:110371641-110371642	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs538347827	chr8:110371684-110371685	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs193124192	chr8:110371694-110371695	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs556160951	chr8:110371760-110371761	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs75557300	chr8:110371768-110371769	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs544534692	chr8:110371771-110371772	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs75894600	chr8:110371796-110371797	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs557906533	chr8:110371806-110371807	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs1458920	chr8:110371809-110371810	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
42	rs369429057	chr8:110371813-110371814	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs184272404	chr8:110371877-110371878	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs575804967	chr8:110371966-110371967	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs188329150	chr8:110372016-110372017	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs560277200	chr8:110372017-110372018	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs111674492	chr8:110372052-110372053	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs532495946	chr8:110372063-110372064	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs181253669	chr8:110372070-110372071	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs543368339	chr8:110372072-110372073	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:101)

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
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Seminomas	18059402	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Pancreatic cancer	21811587	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	21080181	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
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
Colorectal cancer	16774939	CNVD
Autosomal-dominant progressive external ophthalmoplegia	19664747	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Multiple myeloma	16461302	CNVD
Sezary syndrome	18413736	CNVD
Breast cancer	21611746	CNVD
Developmental delay	21147756	CNVD
Congenital diaphragmatic hernia	21525063	CNVD
Gastric cancer	22539939	CNVD
Non-small cell lung cancer	19010865	CNVD
small cell lung cancer	20016488	CNVD
Oral squamous cell carcinoma	21853135	CNVD
Chronic myeloid leukemia	21384125	CNVD
Breast cancer	21364760	CNVD
Colorectal cancer	21645411	CNVD
Pancreatic cancer	17952125	CNVD
T-cell lymphomas	22341440	CNVD
Breast cancer	22522925	CNVD
Prostate cancer	22341455	CNVD

Chromatin state (count:230 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:110364800-110374800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr8:110367400-110372600	Weak transcription	K562	blood
3	chr8:110371200-110374400	Weak transcription	Right Atrium	heart
4	chr8:110372200-110372400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr8:110372400-110374200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
6	chr8:110372600-110373000	Enhancers	K562	blood
7	chr8:110373000-110374000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr8:110373000-110374000	Weak transcription	K562	blood
9	chr8:110374000-110374200	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
10	chr8:110374000-110374200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
11	chr8:110374000-110374200	Enhancers	Brain Germinal Matrix	brain
12	chr8:110374000-110374200	Enhancers	HepG2	liver
13	chr8:110374000-110374400	Bivalent Enhancer	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
14	chr8:110374000-110374400	Flanking Bivalent TSS/Enh	iPS-20b Cell Line	embryonic stem cell
15	chr8:110374000-110374400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
16	chr8:110374000-110375200	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
17	chr8:110374000-110375200	Enhancers	K562	blood
18	chr8:110374000-110375400	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
19	chr8:110374000-110375600	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
20	chr8:110374200-110374400	Flanking Bivalent TSS/Enh	H1 Cell Line	embryonic stem cell
21	chr8:110374200-110374400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
22	chr8:110374200-110374400	Flanking Bivalent TSS/Enh	HUES48 Cell Line	embryonic stem cell
23	chr8:110374200-110374400	Bivalent Enhancer	iPS DF 19.11 Cell Line	embryonic stem cell
24	chr8:110374200-110374400	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
25	chr8:110374200-110374400	Bivalent Enhancer	Cortex derived primary cultured neurospheres	brain
26	chr8:110374200-110374400	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
27	chr8:110374200-110374400	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
28	chr8:110374200-110374400	Enhancers	Adipose Nuclei	Adipose
29	chr8:110374200-110374400	Flanking Active TSS	Brain Germinal Matrix	brain
30	chr8:110374200-110374400	Flanking Bivalent TSS/Enh	Fetal Intestine Small	intestine
31	chr8:110374200-110374400	Enhancers	Pancreas	Pancrea
32	chr8:110374200-110374400	Enhancers	Right Ventricle	heart
33	chr8:110374200-110374400	Flanking Bivalent TSS/Enh	Stomach Mucosa	stomach
34	chr8:110374200-110374400	Bivalent Enhancer	HepG2	liver
35	chr8:110374200-110374400	Enhancers	HUVEC	blood vessel
36	chr8:110374200-110374600	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
37	chr8:110374200-110374600	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
38	chr8:110374200-110374600	Active TSS	Brain Hippocampus Middle	brain
39	chr8:110374200-110374600	Bivalent Enhancer	Left Ventricle	heart
40	chr8:110374200-110374800	Active TSS	Muscle Satellite Cultured Cells	--
41	chr8:110374200-110374800	Active TSS	Duodenum Smooth Muscle	Duodenum
42	chr8:110374200-110374800	Bivalent Enhancer	Fetal Lung	lung
43	chr8:110374200-110374800	Active TSS	NH-A	brain
44	chr8:110374200-110375000	Active TSS	Colon Smooth Muscle	Colon
45	chr8:110374200-110375000	Bivalent Enhancer	Fetal Brain Male	brain
46	chr8:110374200-110375200	Active TSS	H9 Cell Line	embryonic stem cell
47	chr8:110374200-110375200	Flanking Bivalent TSS/Enh	Fetal Stomach	stomach
48	chr8:110374200-110375400	Flanking Bivalent TSS/Enh	HUES6 Cell Line	embryonic stem cell
49	chr8:110374200-110375400	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
50	chr8:110374200-110375600	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell

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