Variant report

Variant	nsv522535
Chromosome Location	chr8:130804293-130844400
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:738)
CpG islands
(count:305)
Chromatin interactive
region (count:12)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:738 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:130838550-130838860	HepG2	liver:	n/a	n/a
2	ATF1	chr8:130837611-130837969	K562	blood:	n/a	n/a
3	ATF2	chr8:130838376-130838826	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF2	chr8:130838408-130838788	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr8:130830587-130830844	H1-hESC	embryonic stem cell:	n/a	n/a
6	BCLAF1	chr8:130838456-130838808	GM12878	blood:	n/a	n/a
7	BHLHE40	chr8:130832512-130832647	K562	blood:	n/a	n/a
8	BHLHE40	chr8:130838466-130838746	GM12878	blood:	n/a	n/a
9	CBX3	chr8:130843864-130844189	K562	blood:	n/a	n/a
10	CBX3	chr8:130810676-130810995	K562	blood:	n/a	n/a
11	CBX3	chr8:130838282-130838834	K562	blood:	n/a	n/a
12	CBX3	chr8:130807988-130808275	K562	blood:	n/a	n/a
13	CBX3	chr8:130807970-130808279	K562	blood:	n/a	n/a
14	CBX3	chr8:130832074-130832738	K562	blood:	n/a	n/a
15	CBX3	chr8:130810532-130811031	K562	blood:	n/a	n/a
16	CEBPB	chr8:130838449-130838794	K562	blood:	n/a	n/a
17	CEBPB	chr8:130838283-130838865	MCF-7	breast:	n/a	n/a
18	CEBPB	chr8:130825818-130825995	H1-hESC	embryonic stem cell:	n/a	n/a
19	CEBPB	chr8:130838452-130838802	A549	lung:	n/a	n/a
20	CEBPB	chr8:130837443-130837748	HepG2	liver:	n/a	chr8:130837558-130837569
21	CEBPB	chr8:130838483-130838766	H1-hESC	embryonic stem cell:	n/a	n/a
22	CEBPB	chr8:130838440-130838827	Hela-S3	cervix:	n/a	n/a
23	CEBPB	chr8:130825839-130826606	IMR90	lung:	n/a	n/a
24	CEBPB	chr8:130830863-130831078	K562	blood:	n/a	chr8:130830981-130830992 chr8:130830983-130830992 chr8:130830981-130830994 chr8:130830981-130830994
25	CREB1	chr8:130838391-130838701	A549	lung:	n/a	n/a
26	CTCF	chr8:130837586-130837845	K562	blood:	n/a	n/a
27	CTCF	chr8:130838176-130839123	HCT-116	colon:	n/a	chr8:130838536-130838549
28	CTCF	chr8:130828051-130828194	Hela-S3	cervix:	n/a	n/a
29	CTCF	chr8:130832460-130832610	Hela-S3	cervix:	n/a	chr8:130832517-130832535 chr8:130832519-130832540 chr8:130832518-130832534
30	CTCF	chr8:130838560-130838710	HFF	foreskin:	n/a	n/a
31	CTCF	chr8:130833360-130833510	GM12878	blood:	n/a	n/a
32	CTCF	chr8:130832420-130832570	HBMEC	blood vessel:	n/a	chr8:130832517-130832535 chr8:130832519-130832540 chr8:130832518-130832534
33	CTCF	chr8:130832359-130832749	H1-hESC	embryonic stem cell:	n/a	chr8:130832517-130832535 chr8:130832519-130832540 chr8:130832518-130832534
34	CTCF	chr8:130832398-130832710	K562	blood:	n/a	chr8:130832517-130832535 chr8:130832519-130832540 chr8:130832518-130832534
35	CTCF	chr8:130828080-130828230	HFF-Myc	foreskin:	n/a	n/a
36	CTCF	chr8:130832016-130832941	SK-N-SH	brain:	n/a	chr8:130832517-130832535 chr8:130832519-130832540 chr8:130832518-130832534 chr8:130832330-130832343
37	CTCF	chr8:130838580-130838730	GM12872	blood:	n/a	n/a
38	CTCF	chr8:130838560-130838710	GM12875	blood:	n/a	n/a
39	CTCF	chr8:130832440-130832590	GM06990	blood:	n/a	chr8:130832517-130832535 chr8:130832519-130832540 chr8:130832518-130832534
40	CTCF	chr8:130838453-130838758	K562	blood:	n/a	chr8:130838536-130838549
41	CTCF	chr8:130828060-130828210	WERI-Rb-1	eye:	n/a	n/a
42	CTCF	chr8:130828000-130828150	HVMF	connective:	n/a	n/a
43	CTCF	chr8:130832440-130832590	BJ	skin:	n/a	chr8:130832517-130832535 chr8:130832519-130832540 chr8:130832518-130832534
44	CTCF	chr8:130838540-130838690	MCF-7	breast:	n/a	n/a
45	CTCF	chr8:130832428-130832652	A549	lung:	n/a	chr8:130832517-130832535 chr8:130832519-130832540 chr8:130832518-130832534
46	CTCF	chr8:130828000-130828150	Hela-S3	cervix:	n/a	n/a
47	CTCF	chr8:130838540-130838690	HPAF	blood vessel:	n/a	n/a
48	CTCF	chr8:130827980-130828130	SAEC	small airway:	n/a	n/a
49	CTCF	chr8:130832186-130832248	GM12878	blood:	n/a	n/a
50	CTCF	chr8:130838540-130838690	HFF-Myc	foreskin:	n/a	n/a

(count:305 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:130838629-130838679	HPAEpiC	pulmonary alveolar:	n/a
2	chr8:130838513-130838563	HL-60	blood:	n/a
3	chr8:130832237-130832287	HPAEpiC	pulmonary alveolar:	n/a
4	chr8:130832237-130832287	Hepatocyte	liver:	n/a
5	chr8:130838432-130838482	HEEpiC	esophagus:	n/a
6	chr8:130838883-130838933	AoSMC	blood vessel:	n/a
7	chr8:130838629-130838679	H1-hESC	embryonic stem cell:	embryo
8	chr8:130832237-130832287	H1-hESC	embryonic stem cell:	embryo
9	chr8:130838432-130838482	SK-N-MC	brain:	n/a
10	chr8:130838513-130838563	CMK	blood:	n/a
11	chr8:130832237-130832287	HepG2	liver:	n/a
12	chr8:130838883-130838933	Jurkat	blood:	n/a
13	chr8:130832237-130832287	LNCaP	prostate:	n/a
14	chr8:130838432-130838482	A549	lung:	n/a
15	chr8:130832237-130832287	ECC-1	luminal epithelium:	n/a
16	chr8:130832237-130832287	T-47D	breast:	n/a
17	chr8:130832237-130832287	PrEC	prostate:	n/a
18	chr8:130832237-130832287	HRCEpiC	kidney:	n/a
19	chr8:130838629-130838679	HEK293	kidney:	embryo
20	chr8:130838432-130838482	HCPEpiC	choroid plexus:	n/a
21	chr8:130832237-130832287	SK-N-MC	brain:	n/a
22	chr8:130838883-130838933	HPAEpiC	pulmonary alveolar:	n/a
23	chr8:130838513-130838563	GM12892	blood:	n/a
24	chr8:130832237-130832287	AG09319	gingival:	n/a
25	chr8:130832237-130832287	SAEC	small airway:	n/a
26	chr8:130838629-130838679	HEEpiC	esophagus:	n/a
27	chr8:130838513-130838563	NH-A	brain:	n/a
28	chr8:130838629-130838679	AoSMC	blood vessel:	n/a
29	chr8:130838883-130838933	AG09319	gingival:	n/a
30	chr8:130838513-130838563	PANC-1	pancreas:	n/a
31	chr8:130838883-130838933	GM19239	blood:	n/a
32	chr8:130838432-130838482	NB4	blood:	n/a
33	chr8:130838432-130838482	MCF-7	breast:	n/a
34	chr8:130838883-130838933	K562	blood:	n/a
35	chr8:130838513-130838563	BJ	skin:	n/a
36	chr8:130838513-130838563	AG04449	skin:	fetal
37	chr8:130838513-130838563	HAEpiC	amniotic membrane:	n/a
38	chr8:130838629-130838679	GM12878	blood:	n/a
39	chr8:130838513-130838563	HCPEpiC	choroid plexus:	n/a
40	chr8:130838629-130838679	SK-N-SH_RA	brain:	n/a
41	chr8:130838629-130838679	CMK	blood:	n/a
42	chr8:130838513-130838563	SAEC	small airway:	n/a
43	chr8:130838513-130838563	AG09309	skin:	n/a
44	chr8:130838883-130838933	AG04449	skin:	fetal
45	chr8:130832237-130832287	AG04449	skin:	fetal
46	chr8:130832237-130832287	HEEpiC	esophagus:	n/a
47	chr8:130832237-130832287	HUVEC	blood vessel:	n/a
48	chr8:130838629-130838679	HepG2	liver:	n/a
49	chr8:130838629-130838679	GM12892	blood:	n/a
50	chr8:130838432-130838482	T-47D	breast:	n/a

(count:12 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:130838576..130840911-chr8:130898985..130901514,2	K562	blood:
2	chr8:130760414..130761002-chr8:130838183..130839066,2	MCF-7	breast:
3	chr8:130831390..130833613-chr8:131027128..131030013,2	K562	blood:
4	chr8:130832873..130834634-chr8:130872875..130874898,2	K562	blood:
5	chr8:130812388..130815875-chr8:130817210..130819491,3	MCF-7	breast:
6	chr8:130838375..130838938-chr8:130903507..130904182,2	MCF-7	breast:
7	chr8:130830092..130833014-chr8:130837793..130842091,3	K562	blood:
8	chr8:130830092..130833014-chr8:130837793..130842091,3	K562	blood:
9	chr8:130830602..130833613-chr8:131027054..131030013,3	K562	blood:
10	chr8:130812388..130815875-chr8:130817210..130819491,3	MCF-7	breast:
11	chr8:130838362..130839036-chr8:130903623..130904767,5	MCF-7	breast:
12	chr7:132179184..132180204-chr8:130838562..130839258,3	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000254317	TF binding region
ENSG00000254317	CpG island
ENSG00000153310	chromatin interactions

Extended variants
information (count: 1609 )
Associated
traits (count: 159 )

Variant overlapped rSNPs/rCNVs (count:1609 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4260864	chr8:130804293-130804294	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs538886379	chr8:130804298-130804299	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs192726909	chr8:130804315-130804316	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs185136210	chr8:130804316-130804317	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs540466068	chr8:130804348-130804349	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs554931325	chr8:130804394-130804395	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs529908154	chr8:130804403-130804404	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs532658993	chr8:130804431-130804432	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs190063956	chr8:130804474-130804475	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs202031401	chr8:130804477-130804478	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs193229402	chr8:130804490-130804491	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs559105105	chr8:130804510-130804511	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs375526340	chr8:130804511-130804512	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs577409721	chr8:130804513-130804514	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs544923951	chr8:130804535-130804536	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs13269983	chr8:130804545-130804546	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs574170098	chr8:130804552-130804553	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs200950440	chr8:130804557-130804558	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs386729986	chr8:130804564-130804565	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs13268387	chr8:130804586-130804587	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs569303950	chr8:130804601-130804602	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs3957254	chr8:130804611-130804612	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs530581735	chr8:130804643-130804644	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs201983829	chr8:130804654-130804655	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs185046407	chr8:130804703-130804704	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs560822816	chr8:130804704-130804705	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs13268232	chr8:130804762-130804763	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs188248201	chr8:130804805-130804806	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs546172780	chr8:130804886-130804887	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs566614170	chr8:130804932-130804933	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs571037474	chr8:130804978-130804979	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs373324553	chr8:130805070-130805071	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs369819206	chr8:130805071-130805072	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs527673478	chr8:130805072-130805073	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs76976591	chr8:130805089-130805090	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs181060910	chr8:130805125-130805126	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs370263245	chr8:130805260-130805261	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs569442937	chr8:130805274-130805275	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs200328957	chr8:130805278-130805279	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs536397648	chr8:130805344-130805345	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs555264585	chr8:130805350-130805351	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs374338997	chr8:130805374-130805375	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs80277867	chr8:130805385-130805386	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs60366798	chr8:130805444-130805445	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs185328943	chr8:130805447-130805448	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs558652310	chr8:130805448-130805449	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs189693835	chr8:130805451-130805452	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs575419977	chr8:130805455-130805456	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs10098559	chr8:130805456-130805457	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs76818163	chr8:130805567-130805568	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:159)

Disease	PMID	Source
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
Testicular cancer	18059402	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21509527	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21248843	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	17603634	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
Acute myeloid leukemia	20729466	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
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
Endometrioid adenocarcinoma	16974079	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
Papillary thyroid cancer	17515504	CNVD
Basal cell lymphoma	17053054	CNVD
Gastric cancer	21528007	CNVD
Breast cancer	22532251	CNVD
Cervical cancer	21062161	CNVD
Cancer	21129771	CNVD
benign familial neonatal convulsions	18472482	CNVD
Breast cancer	16417655	CNVD
Astrocytoma	17387387	CNVD
Cancer	21183584	CNVD
Follicular lymphoma	20505157	CNVD
T-cell lymphomas	19863542	CNVD
Colorectal cancer	20709793	CNVD
Medulloblastoma	20607354	CNVD
Breast cancer	20814816	CNVD
Colorectal cancer	22486879	CNVD
Breast cancer	17908964	CNVD
Colorectal cancer	20031965	CNVD
Hepatocellular carcinoma	16750200	CNVD
Ovarian cancer	17908964	CNVD
Ovarian cancer	20031965	CNVD
Prostate cancer	20031965	CNVD
Non-small cell lung cancer	17643093	CNVD
Prostate cancer	19242612	CNVD
Colorectal cancer	16774939	CNVD
Malignant melanoma	17260012	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Acute myeloid leukemia	17268525	CNVD
Acute myeloid leukemia	18379011	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Sezary syndrome	18413736	CNVD
Breast cancer	22048815	CNVD
Colorectal cancer	16912164	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Lung adenocarcinoma	21148746	CNVD
Lung cancer	21911935	CNVD
Breast cancer	20459607	CNVD
Medulloblastoma	19270706	CNVD
Acute myeloid leukemia	19651601	CNVD
Colorectal cancer	21645411	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Colorectal cancer	19455253	CNVD
Glioblastoma multiforme	22286061	CNVD
Colorectal cancer	22860045	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Lung cancer	17925434	CNVD
Non-small cell lung cancer	21829676	CNVD
Prostate cancer	17217626	CNVD
Cancer	17160897	CNVD
Breast cancer	16497871	CNVD
Colorectal cancer	16882699	CNVD
Cystic fibrosis	19273617	CNVD
Chronic stroke	19622162	CNVD
Chordoma	18071362	CNVD
Breast cancer	17850661	CNVD
head and neck squamous cell carcinoma	16740747	CNVD
Gastric cancer	22539939	CNVD
Breast cancer	16272173	CNVD
Uveal melanoma	20484589	CNVD
Ovarian cancer	20844748	CNVD
Multiple myeloma	16616336	CNVD
Breast cancer	16620391	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Breast cancer	21364760	CNVD
Breast cancer	21611746	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Schizophrenia	23813976	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Cancer	20164919	CNVD
Gastric cancer	22014070	CNVD
T-cell lymphomas	22341440	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:288 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:130801000-130809400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
2	chr8:130801800-130809400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr8:130808400-130808600	ZNF genes & repeats	Primary neutrophils fromperipheralblood	blood
4	chr8:130808400-130809800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
5	chr8:130808400-130811200	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr8:130809200-130810000	Enhancers	NHEK	skin
7	chr8:130809400-130809800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr8:130809400-130810000	Enhancers	HMEC	breast
9	chr8:130809400-130810200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
10	chr8:130809600-130809800	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
11	chr8:130809800-130810000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
12	chr8:130810000-130811200	ZNF genes & repeats	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
13	chr8:130810200-130811400	ZNF genes & repeats	Foreskin Keratinocyte Primary Cells skin03	Skin
14	chr8:130810400-130811200	ZNF genes & repeats	Foreskin Keratinocyte Primary Cells skin02	Skin
15	chr8:130810600-130811200	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
16	chr8:130810800-130811600	ZNF genes & repeats	Monocytes-CD14+_RO01746	blood
17	chr8:130811200-130812000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
18	chr8:130811200-130812200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
19	chr8:130811400-130812000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
20	chr8:130811600-130815200	Weak transcription	Monocytes-CD14+_RO01746	blood
21	chr8:130812000-130812400	Enhancers	NHEK	skin
22	chr8:130812000-130812800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
23	chr8:130812000-130812800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
24	chr8:130812200-130813600	Enhancers	Esophagus	oesophagus
25	chr8:130812200-130813800	Enhancers	HMEC	breast
26	chr8:130812200-130814400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
27	chr8:130812400-130813600	Flanking Active TSS	NHEK	skin
28	chr8:130812600-130813800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
29	chr8:130812600-130814200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
30	chr8:130812600-130814400	Enhancers	Adipose Nuclei	Adipose
31	chr8:130812800-130813200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
32	chr8:130812800-130813200	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
33	chr8:130812800-130813400	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
34	chr8:130813000-130813800	Enhancers	Right Atrium	heart
35	chr8:130813200-130813600	Enhancers	Left Ventricle	heart
36	chr8:130813200-130813800	Enhancers	Right Ventricle	heart
37	chr8:130813200-130814200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
38	chr8:130813400-130814600	Enhancers	Fetal Heart	heart
39	chr8:130813400-130816000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
40	chr8:130813600-130814600	Enhancers	NHEK	skin
41	chr8:130813600-130814800	Weak transcription	Left Ventricle	heart
42	chr8:130813600-130815200	Weak transcription	Esophagus	oesophagus
43	chr8:130813800-130814200	Enhancers	Colon Smooth Muscle	Colon
44	chr8:130813800-130814800	Weak transcription	Right Atrium	heart
45	chr8:130813800-130814800	Weak transcription	Right Ventricle	heart
46	chr8:130814000-130814200	Enhancers	Stomach Smooth Muscle	stomach
47	chr8:130814200-130815200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
48	chr8:130814200-130815200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
49	chr8:130814400-130815200	Weak transcription	Adipose Nuclei	Adipose
50	chr8:130814400-130820800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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