Variant report

Variant	nsv611842
Chromosome Location	chr8:107076421-107115482
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:423)
CpG islands
(count:123)
Chromatin interactive
region (count:16)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:423 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:107093245-107093505	HepG2	liver:	n/a	n/a
2	ATF2	chr8:107107246-107107587	GM12878	blood:	n/a	n/a
3	ATF2	chr8:107098834-107099117	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF2	chr8:107102949-107103278	GM12878	blood:	n/a	n/a
5	BATF	chr8:107102928-107103230	GM12878	blood:	n/a	n/a
6	BATF	chr8:107094846-107095134	GM12878	blood:	n/a	n/a
7	BCL11A	chr8:107094774-107095179	GM12878	blood:	n/a	chr8:107095052-107095061
8	BHLHE40	chr8:107099305-107099506	GM12878	blood:	n/a	n/a
9	BHLHE40	chr8:107094120-107094132	GM12878	blood:	n/a	n/a
10	BHLHE40	chr8:107088754-107088803	K562	blood:	n/a	n/a
11	CBX3	chr8:107089487-107089864	HCT-116	colon:	n/a	n/a
12	CBX3	chr8:107089412-107089774	K562	blood:	n/a	n/a
13	CBX3	chr8:107089317-107089881	HCT-116	colon:	n/a	n/a
14	CBX3	chr8:107089452-107089755	K562	blood:	n/a	n/a
15	CEBPB	chr8:107105654-107105852	HepG2	liver:	n/a	chr8:107105806-107105817
16	CEBPB	chr8:107113805-107114117	HepG2	liver:	n/a	chr8:107113946-107113957
17	CEBPB	chr8:107113815-107114117	IMR90	lung:	n/a	chr8:107113946-107113957
18	CEBPB	chr8:107099477-107099929	HepG2	liver:	n/a	chr8:107099767-107099780
19	CEBPB	chr8:107098492-107098755	IMR90	lung:	n/a	n/a
20	CHD2	chr8:107099469-107099473	GM12878	blood:	n/a	n/a
21	CHD2	chr8:107105297-107105530	K562	blood:	n/a	n/a
22	CHD2	chr8:107094008-107094036	GM12878	blood:	n/a	n/a
23	CTCF	chr8:107093334-107093553	MCF-7	breast:	n/a	n/a
24	CTCF	chr8:107110160-107110310	HA-sp	spinal cord:	n/a	n/a
25	CTCF	chr8:107093340-107093490	GM12868	blood:	n/a	n/a
26	CTCF	chr8:107093340-107093490	GM12865	blood:	n/a	n/a
27	CTCF	chr8:107093380-107093530	GM12873	blood:	n/a	n/a
28	CTCF	chr8:107093369-107093496	GM13976	blood:	n/a	n/a
29	CTCF	chr8:107093340-107093490	GM12875	blood:	n/a	n/a
30	CTCF	chr8:107093020-107093170	GM12878	blood:	n/a	n/a
31	CTCF	chr8:107093300-107093450	GM12872	blood:	n/a	n/a
32	CTCF	chr8:107110100-107110250	HFF	foreskin:	n/a	n/a
33	CTCF	chr8:107093320-107093470	GM12878	blood:	n/a	n/a
34	CTCF	chr8:107093260-107093410	HAc	cerebellar:	n/a	n/a
35	CTCF	chr8:107093320-107093470	HCFaa	heart:	n/a	n/a
36	CTCF	chr8:107093380-107093530	A549	lung:	n/a	n/a
37	CTCF	chr8:107093326-107093514	SK-N-SH_RA	brain:	n/a	n/a
38	CTCF	chr8:107093246-107093551	H1-hESC	embryonic stem cell:	n/a	n/a
39	CTCF	chr8:107093228-107093649	MCF-7	breast:	n/a	n/a
40	CTCF	chr8:107093305-107093526	K562	blood:	n/a	n/a
41	CTCF	chr8:107093195-107093591	H1-hESC	embryonic stem cell:	n/a	n/a
42	CTCF	chr8:107093360-107093510	HFF	foreskin:	n/a	n/a
43	CTCF	chr8:107110120-107110270	AG10803	skin:	n/a	n/a
44	CTCF	chr8:107092974-107093673	HCT-116	colon:	n/a	n/a
45	CTCF	chr8:107093322-107093480	A549	lung:	n/a	n/a
46	CTCF	chr8:107093063-107093148	GM13977	blood:	n/a	n/a
47	CTCF	chr8:107093296-107093563	ProgFib	skin:	n/a	n/a
48	CTCF	chr8:107093300-107093450	HL-60	blood:	n/a	n/a
49	CTCF	chr8:107092680-107092830	GM06990	blood:	n/a	n/a
50	CTCF	chr8:107093071-107093732	MCF-7	breast:	n/a	n/a

(count:123 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:107108787-107108837	ECC-1	luminal epithelium:	n/a
2	chr8:107108787-107108837	ECC-1	luminal epithelium:	n/a
3	chr8:107095959-107096009	HCF	heart:	n/a
4	chr8:107095959-107096009	HRPEpiC	eye:	n/a
5	chr8:107108787-107108837	GM06990	blood:	n/a
6	chr8:107095959-107096009	SK-N-MC	brain:	n/a
7	chr8:107095959-107096009	NB4	blood:	n/a
8	chr8:107095959-107096009	NT2-D1	testis:	n/a
9	chr8:107095959-107096009	ovcar-3	ovarian:	n/a
10	chr8:107095959-107096009	AG04450	lung:	fetal
11	chr8:107095959-107096009	PFSK-1	brain:	n/a
12	chr8:107095959-107096009	HIPEpiC	eye:	n/a
13	chr8:107095959-107096009	GM12892	blood:	n/a
14	chr8:107108787-107108837	Jurkat	blood:	n/a
15	chr8:107108787-107108837	MCF10A-Er-Src	breast:	n/a
16	chr8:107108787-107108837	SK-N-MC	brain:	n/a
17	chr8:107108787-107108837	NHDF-neo	bronchial:	n/a
18	chr8:107095959-107096009	A549	lung:	n/a
19	chr8:107108787-107108837	T-47D	breast:	n/a
20	chr8:107095959-107096009	NH-A	brain:	n/a
21	chr8:107108787-107108837	U87	brain:	n/a
22	chr8:107095959-107096009	HEK293	kidney:	embryo
23	chr8:107108787-107108837	GM12892	blood:	n/a
24	chr8:107095959-107096009	RPTEC	kidney:	n/a
25	chr8:107108787-107108837	LNCaP	prostate:	n/a
26	chr8:107095959-107096009	NHBE	bronchial:	n/a
27	chr8:107095959-107096009	NHDF-neo	bronchial:	n/a
28	chr8:107108787-107108837	ProgFib	skin:	n/a
29	chr8:107108787-107108837	NB4	blood:	n/a
30	chr8:107095959-107096009	Jurkat	blood:	n/a
31	chr8:107095959-107096009	HL-60	blood:	n/a
32	chr8:107108787-107108837	AG09319	gingival:	n/a
33	chr8:107108787-107108837	HCM	heart:	n/a
34	chr8:107095959-107096009	HepG2	liver:	n/a
35	chr8:107095959-107096009	HPAEpiC	pulmonary alveolar:	n/a
36	chr8:107095959-107096009	PANC-1	pancreas:	n/a
37	chr8:107108787-107108837	HCT-116	colon:	n/a
38	chr8:107095959-107096009	HCPEpiC	choroid plexus:	n/a
39	chr8:107108787-107108837	AG09309	skin:	n/a
40	chr8:107108787-107108837	BJ	skin:	n/a
41	chr8:107108787-107108837	AG04450	lung:	fetal
42	chr8:107108787-107108837	H1-hESC	embryonic stem cell:	embryo
43	chr8:107095959-107096009	BJ	skin:	n/a
44	chr8:107095959-107096009	H1-hESC	embryonic stem cell:	embryo
45	chr8:107095959-107096009	Caco-2	colon:	n/a
46	chr8:107108787-107108837	GM12878	blood:	n/a
47	chr8:107108787-107108837	SKMC	muscle:	n/a
48	chr8:107095959-107096009	PrEC	prostate:	n/a
49	chr8:107108787-107108837	HepG2	liver:	n/a
50	chr8:107108787-107108837	HAEpiC	amniotic membrane:	n/a

(count:16 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:107071316..107072942-chr8:107075565..107078465,2	MCF-7	breast:
2	chr8:107085770..107087985-chr8:107092764..107094318,2	MCF-7	breast:
3	chr8:106952270..106952820-chr8:107091540..107092239,2	MCF-7	breast:
4	chr8:107092680..107095598-chr8:107097096..107099230,2	MCF-7	breast:
5	chr8:106951964..106952911-chr8:107092917..107093874,3	MCF-7	breast:
6	chr8:107092975..107093872-chr8:107282203..107282950,2	K562	blood:
7	chr8:107015900..107017263-chr8:107092920..107093525,5	MCF-7	breast:
8	chr8:106945007..106945989-chr8:107093330..107093872,2	K562	blood:
9	chr8:107085770..107087985-chr8:107092764..107094318,2	MCF-7	breast:
10	chr8:107071595..107074143-chr8:107092425..107094759,2	K562	blood:
11	chr8:107059219..107060866-chr8:107093801..107095788,2	K562	blood:
12	chr8:107016577..107017130-chr8:107109768..107110481,2	MCF-7	breast:
13	chr8:107065574..107067380-chr8:107096296..107097895,2	K562	blood:
14	chr8:107071254..107072899-chr8:107075666..107077404,2	K562	blood:
15	chr8:107092680..107095598-chr8:107097096..107099230,2	MCF-7	breast:
16	chr8:106918347..106919345-chr8:107093305..107094021,2	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000251003	TF binding region
ENSG00000251003	CpG island
ENSG00000254615	chromatin interactions
ENSG00000251003	chromatin interactions
ENSG00000164830	chromatin interactions

Extended variants
information (count: 1169 )
Associated
traits (count: 95 )

Variant overlapped rSNPs/rCNVs (count:1169 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs727419	chr8:107076421-107076422	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs200830118	chr8:107076430-107076431	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs564010892	chr8:107076436-107076437	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs570225735	chr8:107076451-107076452	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs537355962	chr8:107076465-107076466	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs184080269	chr8:107076475-107076476	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs534983773	chr8:107076477-107076478	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs373121675	chr8:107076532-107076533	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs576696422	chr8:107076544-107076545	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs553389274	chr8:107076555-107076556	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs578164200	chr8:107076560-107076561	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs545515608	chr8:107076561-107076562	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs376439603	chr8:107076580-107076581	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs201987207	chr8:107076644-107076645	Weak transcription	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs375812641	chr8:107076645-107076646	Weak transcription	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs575354916	chr8:107076651-107076652	Weak transcription	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs142900629	chr8:107076653-107076654	Weak transcription	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs536098919	chr8:107076666-107076667	Weak transcription	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs561207387	chr8:107076746-107076747	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs546480902	chr8:107076754-107076755	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs147428134	chr8:107076768-107076769	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs114482691	chr8:107076832-107076833	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs532119671	chr8:107076935-107076936	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs550249745	chr8:107076980-107076981	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs570160975	chr8:107076994-107076995	Weak transcription	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs137954306	chr8:107076998-107076999	Weak transcription	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs549429339	chr8:107077032-107077033	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs35659250	chr8:107077037-107077038	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs373900989	chr8:107077073-107077074	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs567985221	chr8:107077198-107077199	Weak transcription	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs535315438	chr8:107077202-107077203	Weak transcription Enhancers	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs553452569	chr8:107077217-107077218	Weak transcription Enhancers	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs578063383	chr8:107077218-107077219	Weak transcription Enhancers	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs200174055	chr8:107077241-107077242	Weak transcription Enhancers	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs539145668	chr8:107077282-107077283	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs34958885	chr8:107077288-107077289	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs368046497	chr8:107077300-107077301	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs76080567	chr8:107077302-107077303	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs575370604	chr8:107077344-107077345	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs542770990	chr8:107077363-107077364	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs560005879	chr8:107077383-107077384	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs528660120	chr8:107077384-107077385	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs143970269	chr8:107077395-107077396	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs35330955	chr8:107077412-107077413	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs2082066	chr8:107077454-107077455	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs531936895	chr8:107077458-107077459	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs530850474	chr8:107077472-107077473	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs543999761	chr8:107077524-107077525	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs562571891	chr8:107077572-107077573	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs529739475	chr8:107077586-107077587	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:95)

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
Thoracic aortic aneurysm	21092924	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
small cell lung cancer	20016488	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
Breast cancer	21364760	CNVD
Gastric cancer	22539939	CNVD
Non-small cell lung cancer	19010865	CNVD

Chromatin state (count:331 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:107073600-107078000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr8:107077200-107077600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr8:107077400-107077600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr8:107079200-107082000	Weak transcription	Fetal Heart	heart
5	chr8:107084000-107084400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr8:107084000-107084600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
7	chr8:107089800-107090600	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
8	chr8:107089800-107091600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr8:107090200-107090400	ZNF genes & repeats	Pancreatic Islets	Pancreatic Islet
10	chr8:107090400-107095000	Weak transcription	Pancreatic Islets	Pancreatic Islet
11	chr8:107090600-107099000	Weak transcription	Esophagus	oesophagus
12	chr8:107091400-107091600	Enhancers	NHLF	lung
13	chr8:107091400-107092800	Enhancers	Aorta	Aorta
14	chr8:107091600-107092200	Weak transcription	NHLF	lung
15	chr8:107091800-107092000	Enhancers	Adipose Nuclei	Adipose
16	chr8:107091800-107092600	Enhancers	Brain Anterior Caudate	brain
17	chr8:107091800-107092800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
18	chr8:107091800-107093400	Enhancers	Brain Hippocampus Middle	brain
19	chr8:107092000-107092800	Weak transcription	Adipose Nuclei	Adipose
20	chr8:107092000-107092800	Enhancers	HUVEC	blood vessel
21	chr8:107092200-107092800	Enhancers	Duodenum Smooth Muscle	Duodenum
22	chr8:107092200-107092800	Enhancers	NHLF	lung
23	chr8:107092400-107093000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
24	chr8:107092400-107093000	Enhancers	Ovary	ovary
25	chr8:107092400-107093600	Enhancers	Stomach Smooth Muscle	stomach
26	chr8:107092400-107094800	Enhancers	NH-A	brain
27	chr8:107092400-107095400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
28	chr8:107092400-107096200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
29	chr8:107092400-107096200	Enhancers	Osteobl	bone
30	chr8:107092600-107092800	Enhancers	Duodenum Mucosa	Duodenum
31	chr8:107092600-107093000	Enhancers	Brain Cingulate Gyrus	brain
32	chr8:107092600-107093000	Enhancers	Skeletal Muscle Male	skeletal muscle
33	chr8:107092600-107094200	Weak transcription	Brain Anterior Caudate	brain
34	chr8:107092800-107093000	Flanking Active TSS	HUVEC	blood vessel
35	chr8:107092800-107093200	Weak transcription	Duodenum Smooth Muscle	Duodenum
36	chr8:107092800-107093400	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
37	chr8:107092800-107093400	Weak transcription	Aorta	Aorta
38	chr8:107092800-107094200	Weak transcription	NHLF	lung
39	chr8:107092800-107094400	Enhancers	Muscle Satellite Cultured Cells	--
40	chr8:107092800-107096400	Enhancers	Adipose Nuclei	Adipose
41	chr8:107093000-107093200	Enhancers	HUES48 Cell Line	embryonic stem cell
42	chr8:107093000-107093200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
43	chr8:107093000-107093400	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
44	chr8:107093000-107093400	Weak transcription	Brain Cingulate Gyrus	brain
45	chr8:107093000-107093400	Weak transcription	Ovary	ovary
46	chr8:107093000-107093400	Weak transcription	Skeletal Muscle Male	skeletal muscle
47	chr8:107093000-107093400	Active TSS	HUVEC	blood vessel
48	chr8:107093000-107093400	Enhancers	NHEK	skin
49	chr8:107093000-107095200	Enhancers	Dnd41	blood
50	chr8:107093200-107093400	Weak transcription	Duodenum Mucosa	Duodenum

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