Variant report

Variant	nsv1020285
Chromosome Location	chr7:50229750-50258911
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	chr7:50245007-50245261	K562	blood:	n/a	n/a
2	ARID3A	chr7:50250508-50250519	K562	blood:	n/a	n/a
3	ARID3A	chr7:50236511-50236602	HepG2	liver:	n/a	n/a
4	ARID3A	chr7:50237144-50237408	K562	blood:	n/a	n/a
5	ATF1	chr7:50241704-50242076	K562	blood:	n/a	n/a
6	ATF2	chr7:50237110-50237589	GM12878	blood:	n/a	n/a
7	ATF2	chr7:50250139-50250535	GM12878	blood:	n/a	n/a
8	ATF3	chr7:50237160-50237501	K562	blood:	n/a	n/a
9	ATF3	chr7:50237120-50237561	K562	blood:	n/a	n/a
10	BACH1	chr7:50237215-50237530	K562	blood:	n/a	chr7:50237467-50237481 chr7:50237325-50237339
11	BACH1	chr7:50237114-50237590	H1-hESC	embryonic stem cell:	n/a	chr7:50237467-50237481 chr7:50237325-50237339
12	BACH1	chr7:50246369-50246525	K562	blood:	n/a	n/a
13	BATF	chr7:50247990-50248263	GM12878	blood:	n/a	chr7:50248177-50248187
14	BATF	chr7:50250229-50250485	GM12878	blood:	n/a	n/a
15	BATF	chr7:50250134-50250493	GM12878	blood:	n/a	n/a
16	BATF	chr7:50237167-50237511	GM12878	blood:	n/a	chr7:50237325-50237335 chr7:50237324-50237335
17	BCL11A	chr7:50250179-50250483	GM12878	blood:	n/a	n/a
18	BCL3	chr7:50250122-50250638	GM12878	blood:	n/a	n/a
19	BHLHE40	chr7:50250390-50250605	K562	blood:	n/a	n/a
20	BHLHE40	chr7:50236989-50237575	K562	blood:	n/a	chr7:50237392-50237408
21	BHLHE40	chr7:50245033-50245251	K562	blood:	n/a	n/a
22	BHLHE40	chr7:50245003-50245298	GM12878	blood:	n/a	n/a
23	BHLHE40	chr7:50237244-50237521	GM12878	blood:	n/a	chr7:50237392-50237408
24	BHLHE40	chr7:50241801-50241956	K562	blood:	n/a	n/a
25	BHLHE40	chr7:50239596-50239662	K562	blood:	n/a	n/a
26	BHLHE40	chr7:50246352-50246569	K562	blood:	n/a	n/a
27	BHLHE40	chr7:50241649-50241821	HepG2	liver:	n/a	n/a
28	BHLHE40	chr7:50237247-50237499	HepG2	liver:	n/a	chr7:50237392-50237408
29	BHLHE40	chr7:50254284-50254484	K562	blood:	n/a	n/a
30	CBX3	chr7:50250265-50250618	K562	blood:	n/a	n/a
31	CBX3	chr7:50237006-50237723	HCT-116	colon:	n/a	n/a
32	CBX3	chr7:50237140-50237554	K562	blood:	n/a	n/a
33	CCNT2	chr7:50237162-50237565	K562	blood:	n/a	n/a
34	CCNT2	chr7:50254419-50254582	K562	blood:	n/a	n/a
35	CEBPB	chr7:50250331-50250478	K562	blood:	n/a	n/a
36	CEBPB	chr7:50241914-50242209	K562	blood:	n/a	chr7:50242069-50242080
37	CEBPB	chr7:50244951-50245197	K562	blood:	n/a	n/a
38	CEBPB	chr7:50244908-50245290	H1-hESC	embryonic stem cell:	n/a	n/a
39	CEBPB	chr7:50241927-50242234	HepG2	liver:	n/a	chr7:50242069-50242080
40	CEBPD	chr7:50254363-50254766	K562	blood:	n/a	n/a
41	CHD2	chr7:50253013-50253187	GM12878	blood:	n/a	n/a
42	CHD2	chr7:50245032-50245283	GM12878	blood:	n/a	n/a
43	CHD2	chr7:50237252-50237486	GM12878	blood:	n/a	n/a
44	CREB1	chr7:50241631-50241997	HepG2	liver:	n/a	n/a
45	CTCF	chr7:50252387-50252436	GM13977	blood:	n/a	chr7:50252398-50252416 chr7:50252401-50252410
46	CTCF	chr7:50244832-50245425	K562	blood:	n/a	chr7:50245110-50245128 chr7:50245115-50245125 chr7:50245113-50245126 chr7:50245112-50245133 chr7:50245111-50245127
47	CTCF	chr7:50245020-50245170	SK-N-SH_RA	brain:	n/a	chr7:50245110-50245128 chr7:50245115-50245125 chr7:50245113-50245126 chr7:50245112-50245133 chr7:50245111-50245127
48	CTCF	chr7:50252645-50252649	GM12891	blood:	n/a	n/a
49	CTCF	chr7:50252340-50252490	GM12873	blood:	n/a	chr7:50252398-50252416 chr7:50252401-50252410
50	CTCF	chr7:50245000-50245150	HFF-Myc	foreskin:	n/a	chr7:50245110-50245128 chr7:50245115-50245125 chr7:50245113-50245126 chr7:50245112-50245133 chr7:50245111-50245127

No.	Distal block	Cell Line	Cell type
1	chr7:50244603..50245562-chr7:50436820..50437380,2	MCF-7	breast:
2	chr7:50252064..50252875-chr7:50343781..50344565,2	NB4	blood:
3	chr7:50238172..50240655-chr7:50240839..50242748,2	K562	blood:
4	chr7:50257452..50260269-chr7:50267276..50269826,2	K562	blood:
5	chr7:50244998..50245577-chr7:50424453..50425223,2	K562	blood:
6	chr7:50235390..50237787-chr7:50242570..50244249,2	K562	blood:
7	chr7:50235390..50238226-chr7:50241670..50244249,2	K562	blood:
8	chr7:50253030..50255568-chr7:50314396..50316828,2	K562	blood:
9	chr7:50246034..50246838-chr7:50436681..50437592,4	K562	blood:
10	chr7:50241107..50243167-chr7:50244986..50246835,3	K562	blood:
11	chr7:50237645..50240143-chr7:50344951..50346541,2	K562	blood:
12	chr7:50225790..50228475-chr7:50229691..50231386,2	K562	blood:
13	chr7:50251815..50254720-chr7:50262082..50263652,2	K562	blood:
14	chr7:50244742..50245855-chr7:50436595..50438226,13	K562	blood:
15	chr7:50244683..50245796-chr7:50436572..50437838,9	MCF-7	breast:
16	chr7:50253301..50255732-chr7:50349910..50352191,2	K562	blood:
17	chr7:50243616..50247294-chr7:50434768..50437607,4	K562	blood:
18	chr7:50241573..50244782-chr7:50244911..50249106,3	K562	blood:
19	chr7:50244573..50245590-chr7:50485442..50486430,7	MCF-7	breast:
20	chr7:50249185..50251985-chr7:50254623..50256647,2	K562	blood:
21	chr7:50244500..50246080-chr7:50485390..50486198,6	K562	blood:
22	chr7:50250013..50252117-chr7:50353490..50355323,2	K562	blood:
23	chr7:50244968..50246588-chr7:50352625..50355039,2	K562	blood:
24	chr7:50247609..50248195-chr7:50485491..50486034,2	K562	blood:
25	chr7:50249185..50251985-chr7:50254623..50256647,2	K562	blood:
26	chr7:50241107..50243167-chr7:50244986..50246835,3	K562	blood:
27	chr7:50238172..50240655-chr7:50240839..50242748,2	K562	blood:
28	chr7:50245054..50247899-chr7:50345747..50347380,2	K562	blood:
29	chr7:50244665..50245593-chr7:50485405..50486013,4	MCF-7	breast:
30	chr7:50226331..50229120-chr7:50229691..50231704,3	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZPBP-2	chr7:50241835-50242586	XLOC_006438
2	lnc-ZPBP-2	chr7:50243859-50243914	XLOC_006438

Variant related genes	Relation type
ENSG00000231681	TF binding region
ENSG00000235620	chromatin interactions
ENSG00000231681	chromatin interactions
ENSG00000185811	chromatin interactions

Extended variants
information (count: 1189 )
Associated
traits (count: 127 )

Variant overlapped rSNPs/rCNVs (count:1189 , 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	rs10261932	chr7:50229750-50229751	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs142005696	chr7:50229752-50229753	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs143028161	chr7:50229790-50229791	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs187432074	chr7:50229812-50229813	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs190505330	chr7:50229854-50229855	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs377185931	chr7:50229877-50229878	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs529821365	chr7:50229878-50229879	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs528185013	chr7:50229879-50229880	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs148155810	chr7:50229894-50229895	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs183110965	chr7:50229906-50229907	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs530497481	chr7:50229925-50229926	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs551005959	chr7:50229933-50229934	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs141106101	chr7:50230008-50230009	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs115320593	chr7:50230037-50230038	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs187083513	chr7:50230072-50230073	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs549561859	chr7:50230073-50230074	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs190379866	chr7:50230074-50230075	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs535537161	chr7:50230095-50230096	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs555366754	chr7:50230121-50230122	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs150237971	chr7:50230194-50230195	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs534400319	chr7:50230202-50230203	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs556982072	chr7:50230206-50230207	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs117625197	chr7:50230237-50230238	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs546060864	chr7:50230239-50230240	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs555710791	chr7:50230265-50230266	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs553189736	chr7:50230292-50230293	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs138977716	chr7:50230297-50230298	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs182789499	chr7:50230309-50230310	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs561787542	chr7:50230381-50230382	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs541416899	chr7:50230427-50230428	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs550429132	chr7:50230469-50230470	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs530433004	chr7:50230498-50230499	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs571882826	chr7:50230500-50230501	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs544148286	chr7:50230538-50230539	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs142025048	chr7:50230573-50230574	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs533665620	chr7:50230590-50230591	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs546823018	chr7:50230618-50230619	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs538989616	chr7:50230662-50230663	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs187767480	chr7:50230682-50230683	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs74611647	chr7:50230700-50230701	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs569290265	chr7:50230711-50230712	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs537902055	chr7:50230733-50230734	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs551743927	chr7:50230758-50230759	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs570689017	chr7:50230779-50230780	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs146344997	chr7:50230870-50230871	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs12669965	chr7:50230886-50230887	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs138212431	chr7:50230922-50230923	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs572161007	chr7:50230954-50230955	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs535602772	chr7:50231056-50231057	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs546099680	chr7:50231060-50231061	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:127)

Disease	PMID	Source
Glioblastoma multiforme	17387387	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Biliary cancer	19435499	CNVD
Wilms tumour	21544195	CNVD
Neuroblastoma	18923191	CNVD
Glioma	21971842	CNVD
Glioblastoma multiforme	21080181	CNVD
Liposarcoma	21253554	CNVD
Medulloblastoma	21979893	CNVD
Oligodendroglial tumors	17285580	CNVD
Oral cancer	21386901	CNVD
colon cancer	17210682	CNVD
Lung adenocarcinoma	21810691	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Colorectal cancer	19359472	CNVD
Hypothalamic hamartomas	18252217	CNVD
Human rectal carcinomas	16397240	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Medulloblastoma	18056178	CNVD
Basal cell lymphoma	17170743	CNVD
Ewing''s sarcoma	21437220	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
T-cell lymphomas	19863542	CNVD
Malaria	21533027	CNVD
Melanoma	18172304	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Lung cancer	18438408	CNVD
lymphocytic leukemia	21291569	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Cancer	21637783	CNVD
Squamous cell cancer	20885788	CNVD
Breast cancer	16397240	CNVD
Non-small cell lung cancer	21829676	CNVD
Glioblastoma multiforme	17002787	CNVD
Autism	22495311	CNVD
Glioblastoma multiforme	18628472	CNVD
Cancer	21183584	CNVD
Breast cancer	21785460	CNVD
Follicular lymphoma	20505157	CNVD
Williams-beuren syndrome	22470819	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	21364760	CNVD
Acute myeloid leukemia	21251322	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Multiple myeloma	16461302	CNVD
Glioblastoma multiforme	21750150	CNVD
Hepatocellular carcinoma	16750200	CNVD
Acute myeloid leukemia	17237825	CNVD
Gastric cancer	24379144	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Esophageal cancer	21851588	CNVD
Non-small cell lung cancer	17643093	CNVD
Ovarian cancer	18182111	CNVD
Colorectal cancer	16272173	CNVD
Glioblastoma multiforme	17369134	CNVD
Barrett''s esophagus	18559552	CNVD
head and neck squamous cell carcinoma	16943533	CNVD
Anaplastic thyroid cancer	17079354	CNVD
Basal-like breast cancer	17875215	CNVD
Colorectal cancer	16882699	CNVD
Colorectal cancer	18794099	CNVD
Gastrointestinal stromal cancer	17643098	CNVD
Lung cancer	18381415	CNVD
Metastatic colorectal cancer	17664472	CNVD
Non-small cell lung cancer	19255323	CNVD
Non-small cell lung cancer	17673923	CNVD
Non-small cell lung cancer	17975165	CNVD
Non-small cell lung cancer	19622585	CNVD
Ovarian cancer	16607561	CNVD
Squamous cell cancer	19670535	CNVD
head and neck squamous cell carcinoma	16818711	CNVD
small cell lung cancer	18829487	CNVD
Breast cancer	17661082	CNVD
Adenocarcinoma	19260752	CNVD
Esophageal cancer	16575012	CNVD
Lung adenocarcinoma	19138956	CNVD
Lung adenocarcinoma	18379350	CNVD
Lung adenocarcinoma	18258923	CNVD
Lung cancer	19138956	CNVD
Lung cancer	18379350	CNVD
Lung cancer	18258923	CNVD
Non-small cell lung cancer	18304967	CNVD
Non-small cell lung cancer	19451690	CNVD
Non-small cell lung cancer	19260752	CNVD
Non-small cell lung cancer	17079354	CNVD
Non-small cell lung cancer	18559607	CNVD
Rectal cancer	19506820	CNVD
Triple-negative breast cancer	18950515	CNVD
head and neck squamous cell carcinoma	18813952	CNVD
Non-small cell lung cancer	17504988	CNVD
Non-small cell lung cancer	16943533	CNVD
Non-small cell lung cancer	18509184	CNVD
head and neck squamous cell carcinoma	17538160	CNVD
Colorectal cancer	19712476	CNVD
Lung adenocarcinoma	19525976	CNVD
Lung cancer	19525976	CNVD
Lung cancer	19671679	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
small cell lung cancer	20016488	CNVD
Lissencephaly	21572526	CNVD
Breast cancer	17603634	CNVD
Acute myeloid leukemia	16864856	CNVD
Acute lymphoblastic leukemia	18768390	CNVD
Multiple myeloma	16616336	CNVD
Hirschsprung''s Disease	21712996	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Pancreatic cancer	17952125	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
early-passage human iPS cells	21368824	CNVD

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:50228800-50230600	Enhancers	Adipose Nuclei	Adipose
2	chr7:50230000-50230400	Enhancers	Right Atrium	heart
3	chr7:50230600-50239000	Weak transcription	Adipose Nuclei	Adipose
4	chr7:50231200-50231800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
5	chr7:50232800-50233000	Bivalent Enhancer	K562	blood
6	chr7:50234200-50234400	Enhancers	Fetal Thymus	thymus
7	chr7:50234400-50235800	Weak transcription	Fetal Thymus	thymus
8	chr7:50235000-50235800	Enhancers	Fetal Stomach	stomach
9	chr7:50235800-50236200	Weak transcription	Fetal Stomach	stomach
10	chr7:50235800-50240200	Enhancers	Fetal Thymus	thymus
11	chr7:50236000-50236800	Enhancers	HepG2	liver
12	chr7:50236000-50237600	Enhancers	K562	blood
13	chr7:50236200-50237000	Enhancers	Fetal Stomach	stomach
14	chr7:50236200-50237400	Enhancers	Thymus	Thymus
15	chr7:50236200-50238200	Enhancers	Primary T helper cells PMA-I stimulated	--
16	chr7:50236400-50237200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
17	chr7:50236600-50237200	Enhancers	ES-I3 Cell Line	embryonic stem cell
18	chr7:50236600-50237200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
19	chr7:50236600-50237400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
20	chr7:50236800-50237000	Enhancers	Lung	lung
21	chr7:50236800-50237000	Flanking Active TSS	HepG2	liver
22	chr7:50236800-50237200	Enhancers	Fetal Intestine Small	intestine
23	chr7:50236800-50237400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
24	chr7:50236800-50237400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
25	chr7:50236800-50237400	Enhancers	HUES6 Cell Line	embryonic stem cell
26	chr7:50236800-50237600	Enhancers	GM12878-XiMat	blood
27	chr7:50236800-50237800	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
28	chr7:50237000-50237400	Enhancers	Placenta	Placenta
29	chr7:50237000-50237600	Enhancers	H1 Cell Line	embryonic stem cell
30	chr7:50237000-50237600	Enhancers	HUES48 Cell Line	embryonic stem cell
31	chr7:50237000-50237600	Enhancers	HUES64 Cell Line	embryonic stem cell
32	chr7:50237000-50237600	Enhancers	iPS-15b Cell Line	embryonic stem cell
33	chr7:50237000-50237600	Enhancers	iPS-18 Cell Line	embryonic stem cell
34	chr7:50237000-50237800	Enhancers	HepG2	liver
35	chr7:50237200-50244000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
36	chr7:50237400-50237600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
37	chr7:50237400-50240600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
38	chr7:50237400-50241600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
39	chr7:50237400-50241800	Weak transcription	Thymus	Thymus
40	chr7:50237600-50238800	Weak transcription	GM12878-XiMat	blood
41	chr7:50237600-50239000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
42	chr7:50237600-50239400	Weak transcription	K562	blood
43	chr7:50237800-50241200	Weak transcription	HepG2	liver
44	chr7:50238200-50243200	Weak transcription	Primary T helper cells PMA-I stimulated	--
45	chr7:50238800-50239400	Enhancers	GM12878-XiMat	blood
46	chr7:50239000-50240000	Enhancers	Adipose Nuclei	Adipose
47	chr7:50239000-50240400	Enhancers	Primary hematopoietic stem cells short term culture	blood
48	chr7:50239000-50240800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
49	chr7:50239200-50240200	Enhancers	Monocytes-CD14+_RO01746	blood
50	chr7:50239200-50240400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--

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