Variant report

Variant	esv1835599
Chromosome Location	chr6:131554291-131590766
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:223)
CpG islands
(count:122)
Chromatin interactive
region (count:5)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:223 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CEBPB	chr6:131582109-131582484	IMR90	lung:	n/a	chr6:131582286-131582297
2	CEBPB	chr6:131582178-131582378	Hela-S3	cervix:	n/a	chr6:131582286-131582297
3	CEBPB	chr6:131577143-131577459	MCF-7	breast:	n/a	n/a
4	CEBPB	chr6:131582205-131582493	A549	lung:	n/a	chr6:131582286-131582297
5	CEBPB	chr6:131582116-131582482	HepG2	liver:	n/a	chr6:131582286-131582297
6	CEBPB	chr6:131582226-131582427	ECC-1	luminal epithelium:	n/a	chr6:131582286-131582297
7	CEBPB	chr6:131582120-131582439	A549	lung:	n/a	chr6:131582286-131582297
8	CEBPB	chr6:131582186-131582336	HepG2	liver:	n/a	chr6:131582286-131582297
9	CEBPB	chr6:131577172-131577461	ECC-1	luminal epithelium:	n/a	n/a
10	CEBPB	chr6:131582113-131582490	K562	blood:	n/a	chr6:131582286-131582297
11	CEBPB	chr6:131576952-131576993	A549	lung:	n/a	chr6:131576977-131576988
12	CEBPB	chr6:131582217-131582449	A549	lung:	n/a	chr6:131582286-131582297
13	CEBPB	chr6:131582217-131582400	MCF-7	breast:	n/a	chr6:131582286-131582297
14	CEBPB	chr6:131577153-131577476	Hela-S3	cervix:	n/a	n/a
15	CEBPB	chr6:131582217-131582460	ECC-1	luminal epithelium:	n/a	chr6:131582286-131582297
16	CEBPB	chr6:131576865-131577396	IMR90	lung:	n/a	chr6:131576977-131576988
17	CEBPB	chr6:131576884-131577411	H1-hESC	embryonic stem cell:	n/a	chr6:131576977-131576988
18	CEBPB	chr6:131576868-131577048	HepG2	liver:	n/a	chr6:131576977-131576988
19	CEBPB	chr6:131582125-131582475	H1-hESC	embryonic stem cell:	n/a	chr6:131582286-131582297
20	CTCF	chr6:131583359-131583465	MCF-7	breast:	n/a	n/a
21	CTCF	chr6:131583340-131583490	AG04450	lung:	n/a	n/a
22	CTCF	chr6:131583340-131583490	HEK293	kidney:	n/a	n/a
23	CTCF	chr6:131583400-131583550	BJ	skin:	n/a	n/a
24	CTCF	chr6:131571260-131571410	AG10803	skin:	n/a	n/a
25	CTCF	chr6:131583340-131583490	HMF	breast:	n/a	n/a
26	CTCF	chr6:131583341-131583499	HepG2	liver:	n/a	n/a
27	CTCF	chr6:131583300-131583450	HPF	lung:	n/a	n/a
28	CTCF	chr6:131571260-131571410	SAEC	small airway:	n/a	n/a
29	CTCF	chr6:131583272-131583634	MCF-7	breast:	n/a	n/a
30	CTCF	chr6:131577200-131577350	HCPEpiC	choroid plexus:	n/a	n/a
31	CTCF	chr6:131571360-131571510	AG09319	gingival:	n/a	n/a
32	CTCF	chr6:131583320-131583470	SK-N-SH_RA	brain:	n/a	n/a
33	CTCF	chr6:131571440-131571590	RPTEC	kidney:	n/a	n/a
34	CTCF	chr6:131583356-131583492	A549	lung:	n/a	n/a
35	CTCF	chr6:131583373-131583466	NHEK	skin:	n/a	n/a
36	CTCF	chr6:131583400-131583550	MCF-7	breast:	n/a	n/a
37	CTCF	chr6:131583360-131583510	NHEK	skin:	n/a	n/a
38	CTCF	chr6:131583380-131583530	NB4	blood:	n/a	n/a
39	CTCF	chr6:131583320-131583470	HepG2	liver:	n/a	n/a
40	CTCF	chr6:131577236-131577282	MCF-7	breast:	n/a	n/a
41	CTCF	chr6:131571560-131571710	AG10803	skin:	n/a	n/a
42	CTCF	chr6:131571200-131571350	HMF	breast:	n/a	n/a
43	CTCF	chr6:131583271-131583497	HepG2	liver:	n/a	n/a
44	CTCF	chr6:131571260-131571410	HRPEpiC	eye:	n/a	n/a
45	CTCF	chr6:131583366-131583458	GM12892	blood:	n/a	n/a
46	CTCF	chr6:131583213-131583533	K562	blood:	n/a	n/a
47	CTCF	chr6:131583120-131583270	HVMF	connective:	n/a	n/a
48	CTCF	chr6:131583320-131583470	AG04449	skin:	n/a	n/a
49	CTCF	chr6:131583340-131583490	Caco-2	colon:	n/a	n/a
50	CTCF	chr6:131571500-131571650	HCM	heart:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:131571669-131571719	HNPCEpiC	eye:	n/a
2	chr6:131571669-131571719	H1-hESC	embryonic stem cell:	embryo
3	chr6:131571435-131571485	HNPCEpiC	eye:	n/a
4	chr6:131571435-131571485	HEK293	kidney:	embryo
5	chr6:131571669-131571719	T-47D	breast:	n/a
6	chr6:131571669-131571719	Hepatocyte	liver:	n/a
7	chr6:131571435-131571485	SAEC	small airway:	n/a
8	chr6:131571435-131571485	Jurkat	blood:	n/a
9	chr6:131571669-131571719	SK-N-MC	brain:	n/a
10	chr6:131571669-131571719	HIPEpiC	eye:	n/a
11	chr6:131571435-131571485	AG04449	skin:	fetal
12	chr6:131571669-131571719	HPAEpiC	pulmonary alveolar:	n/a
13	chr6:131571435-131571485	SK-N-SH	brain:	n/a
14	chr6:131571435-131571485	PrEC	prostate:	n/a
15	chr6:131571669-131571719	RPTEC	kidney:	n/a
16	chr6:131571435-131571485	HMEC	breast:	n/a
17	chr6:131571435-131571485	IMR90	lung:	fetal
18	chr6:131571435-131571485	HCM	heart:	n/a
19	chr6:131571669-131571719	GM12891	blood:	n/a
20	chr6:131571435-131571485	HCF	heart:	n/a
21	chr6:131571669-131571719	HRE	kidney:	n/a
22	chr6:131571669-131571719	CMK	blood:	n/a
23	chr6:131571435-131571485	HAEpiC	amniotic membrane:	n/a
24	chr6:131571435-131571485	NB4	blood:	n/a
25	chr6:131571669-131571719	HL-60	blood:	n/a
26	chr6:131571669-131571719	K562	blood:	n/a
27	chr6:131571669-131571719	SKMC	muscle:	n/a
28	chr6:131571435-131571485	AG09309	skin:	n/a
29	chr6:131571669-131571719	GM12878	blood:	n/a
30	chr6:131571435-131571485	Caco-2	colon:	n/a
31	chr6:131571669-131571719	NHDF-neo	bronchial:	n/a
32	chr6:131571435-131571485	CMK	blood:	n/a
33	chr6:131571435-131571485	SKMC	muscle:	n/a
34	chr6:131571669-131571719	PANC-1	pancreas:	n/a
35	chr6:131571669-131571719	PrEC	prostate:	n/a
36	chr6:131571435-131571485	AoSMC	blood vessel:	n/a
37	chr6:131571435-131571485	BJ	skin:	n/a
38	chr6:131571669-131571719	HRPEpiC	eye:	n/a
39	chr6:131571435-131571485	NHBE	bronchial:	n/a
40	chr6:131571669-131571719	IMR90	lung:	fetal
41	chr6:131571669-131571719	HUVEC	blood vessel:	n/a
42	chr6:131571669-131571719	AoSMC	blood vessel:	n/a
43	chr6:131571669-131571719	U87	brain:	n/a
44	chr6:131571669-131571719	NHBE	bronchial:	n/a
45	chr6:131571669-131571719	ovcar-3	ovarian:	n/a
46	chr6:131571669-131571719	HCPEpiC	choroid plexus:	n/a
47	chr6:131571669-131571719	Jurkat	blood:	n/a
48	chr6:131571435-131571485	HCPEpiC	choroid plexus:	n/a
49	chr6:131571669-131571719	HEK293	kidney:	embryo
50	chr6:131571669-131571719	AG09319	gingival:	n/a

(count:5 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:131562493..131564861-chr6:131566716..131568915,2	MCF-7	breast:
2	chr6:131562493..131564861-chr6:131566716..131568915,2	MCF-7	breast:
3	chr6:131574679..131577194-chr6:131577773..131580608,2	MCF-7	breast:
4	chr6:131520473..131521448-chr6:131582980..131583832,4	MCF-7	breast:
5	chr6:131574679..131577194-chr6:131577773..131580608,2	MCF-7	breast:

No data

Variant related genes	Relation type
AKAP7	TF binding region
AKAP7	CpG island
ENSG00000118507	chromatin interactions

Extended variants
information (count: 1288 )
Associated
traits (count: 80 )

Variant overlapped rSNPs/rCNVs (count:1288 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs368797088	chr6:131554291-131554292	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs9492870	chr6:131554349-131554350	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs114524014	chr6:131554384-131554385	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs79772772	chr6:131554435-131554436	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs373275317	chr6:131554442-131554443	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs192735595	chr6:131554443-131554444	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs561333362	chr6:131554454-131554455	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs528996457	chr6:131554457-131554458	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs547087664	chr6:131554467-131554468	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs34871354	chr6:131554492-131554493	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs559137926	chr6:131554504-131554505	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs527897829	chr6:131554521-131554522	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs4897505	chr6:131554553-131554554	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs76777822	chr6:131554562-131554563	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs77455584	chr6:131554568-131554569	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs550230598	chr6:131554640-131554641	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs540998129	chr6:131554674-131554675	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs568454149	chr6:131554675-131554676	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs376800627	chr6:131554679-131554680	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs535997222	chr6:131554714-131554715	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs115923017	chr6:131554744-131554745	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs540873403	chr6:131554887-131554888	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs9321279	chr6:131554909-131554910	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs557639215	chr6:131554911-131554912	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs182368493	chr6:131554939-131554940	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs543305141	chr6:131554949-131554950	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs554992425	chr6:131555041-131555042	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs17060127	chr6:131555302-131555303	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs1570348	chr6:131555391-131555392	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs559417988	chr6:131555416-131555417	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs532862547	chr6:131555420-131555421	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs546408011	chr6:131555421-131555422	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs544256821	chr6:131555499-131555500	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs532082368	chr6:131555535-131555536	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs550490618	chr6:131555563-131555564	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs149685069	chr6:131555573-131555574	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs187259344	chr6:131555600-131555601	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs34409673	chr6:131555623-131555624	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs145520736	chr6:131555634-131555635	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs148865525	chr6:131555646-131555647	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs142617794	chr6:131555659-131555660	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs1923620	chr6:131555673-131555674	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs372893678	chr6:131555691-131555692	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs191667795	chr6:131555747-131555748	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs184673236	chr6:131555774-131555775	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs9492871	chr6:131555850-131555851	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs555251742	chr6:131555869-131555870	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs573567299	chr6:131555880-131555881	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs9492872	chr6:131555944-131555945	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs189051200	chr6:131555946-131555947	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:80)

Disease	PMID	Source
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Biliary cancer	19435499	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	21448237	CNVD
Autism	22495311	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Neuroblastoma	18923191	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Melanoma	18172304	CNVD
Cancer	21637783	CNVD
Colorectal cancer	16272173	CNVD
Gastric cancer	17908304	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	19010834	CNVD
Non-small cell lung cancer	21044232	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	16608533	CNVD
Non-small cell lung cancer	21385341	CNVD
Prostate cancer	16705090	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Ependymoma	16718352	CNVD
High-proliferative meningiomas	17937814	CNVD
Intracranial tumor	16823260	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	16272173	CNVD
Prostate cancer	18632612	CNVD
Wilms tumour	21544195	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Glioma	21046410	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Zellweger syndrome	21572526	CNVD
Follicular lymphoma	20505157	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Malignant melanoma	18718029	CNVD
Lung adenocarcinoma	21935476	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21858162	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	17603634	CNVD
Chondromyxoid Fibroma	20696777	CNVD
Cancer	21183584	CNVD
Developmental delay	19490664	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	21785460	CNVD
Kartagener syndrome	16639409	CNVD
Breast cancer	17133270	CNVD
Follicular lymphoma	18703704	CNVD
Neurodevelopmental disorder	22521361	CNVD
small cell lung cancer	20016488	CNVD
Adenoid cystic carcinoma	18698036	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Leukemia	18688285	CNVD
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Renal cell carcinoma	18592004	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:694 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:131535200-131562200	Weak transcription	Primary hematopoietic stem cells	blood
2	chr6:131535400-131555200	Weak transcription	Brain Hippocampus Middle	brain
3	chr6:131543000-131571200	Weak transcription	Adipose Nuclei	Adipose
4	chr6:131546600-131554600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
5	chr6:131546600-131565400	Weak transcription	Primary T helper cells PMA-I stimulated	--
6	chr6:131546600-131565600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
7	chr6:131546600-131566000	Weak transcription	Primary T helper cells fromperipheralblood	blood
8	chr6:131547800-131554800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
9	chr6:131553400-131554400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
10	chr6:131553400-131555200	Weak transcription	HUES64 Cell Line	embryonic stem cell
11	chr6:131553600-131555000	Weak transcription	HUES48 Cell Line	embryonic stem cell
12	chr6:131553600-131555000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
13	chr6:131553600-131555200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr6:131554400-131554600	Enhancers	iPS-18 Cell Line	embryonic stem cell
15	chr6:131554400-131556000	Enhancers	Cortex derived primary cultured neurospheres	brain
16	chr6:131554600-131554800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
17	chr6:131554600-131555000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
18	chr6:131554800-131555800	Enhancers	iPS-15b Cell Line	embryonic stem cell
19	chr6:131555000-131555600	Enhancers	HUES48 Cell Line	embryonic stem cell
20	chr6:131555000-131555600	Enhancers	iPS-18 Cell Line	embryonic stem cell
21	chr6:131555000-131555600	Enhancers	iPS-20b Cell Line	embryonic stem cell
22	chr6:131555200-131555400	Enhancers	Brain Hippocampus Middle	brain
23	chr6:131555200-131555600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
24	chr6:131555200-131555600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
25	chr6:131555200-131555800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr6:131555200-131555800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
27	chr6:131555200-131555800	Enhancers	HUES6 Cell Line	embryonic stem cell
28	chr6:131555200-131555800	Enhancers	HUES64 Cell Line	embryonic stem cell
29	chr6:131555200-131555800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
30	chr6:131555200-131555800	Enhancers	Pancreatic Islets	Pancreatic Islet
31	chr6:131555400-131555600	Weak transcription	Brain Hippocampus Middle	brain
32	chr6:131559600-131565400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
33	chr6:131559800-131571200	Weak transcription	Liver	Liver
34	chr6:131561800-131562600	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
35	chr6:131561800-131562600	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
36	chr6:131561800-131564400	Weak transcription	Pancreas	Pancrea
37	chr6:131562000-131565400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
38	chr6:131562200-131562400	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
39	chr6:131562200-131562600	ZNF genes & repeats	Primary T cells from cord blood	blood
40	chr6:131562200-131562600	ZNF genes & repeats	Primary hematopoietic stem cells	blood
41	chr6:131562400-131563000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
42	chr6:131562600-131570800	Weak transcription	Primary T cells from cord blood	blood
43	chr6:131562600-131571200	Weak transcription	Primary hematopoietic stem cells	blood
44	chr6:131562600-131571400	Weak transcription	H9 Cell Line	embryonic stem cell
45	chr6:131563000-131580000	Weak transcription	Small Intestine	intestine
46	chr6:131563800-131564000	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
47	chr6:131563800-131564400	Enhancers	Psoas Muscle	Psoas
48	chr6:131564000-131564200	Enhancers	Primary T killer memory cells from peripheral blood	blood
49	chr6:131564000-131565600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
50	chr6:131564000-131565800	Enhancers	Fetal Heart	heart

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links