Variant report

Variant	nsv432612
Chromosome Location	chr4:74723372-74774372
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	chr4:74770214-74770556	K562	blood:	n/a	n/a
2	ARID3A	chr4:74768180-74768191	K562	blood:	n/a	n/a
3	ARID3A	chr4:74751438-74751693	K562	blood:	n/a	n/a
4	ARID3A	chr4:74730276-74730476	K562	blood:	n/a	n/a
5	ARID3A	chr4:74766759-74766935	K562	blood:	n/a	n/a
6	ARID3A	chr4:74734009-74734059	K562	blood:	n/a	n/a
7	ATF1	chr4:74731559-74731693	K562	blood:	n/a	n/a
8	BACH1	chr4:74734856-74734993	H1-hESC	embryonic stem cell:	n/a	n/a
9	BHLHE40	chr4:74770149-74770443	K562	blood:	n/a	n/a
10	BHLHE40	chr4:74766662-74767013	K562	blood:	n/a	n/a
11	BHLHE40	chr4:74735148-74735239	K562	blood:	n/a	n/a
12	BRCA1	chr4:74751592-74752069	Hela-S3	cervix:	n/a	n/a
13	CBX3	chr4:74730039-74730365	K562	blood:	n/a	n/a
14	CCNT2	chr4:74770213-74770535	K562	blood:	n/a	n/a
15	CEBPB	chr4:74762160-74762429	IMR90	lung:	n/a	n/a
16	CEBPB	chr4:74736106-74736228	HepG2	liver:	n/a	chr4:74736180-74736193 chr4:74736180-74736191 chr4:74736181-74736192 chr4:74736180-74736193 chr4:74736182-74736191
17	CEBPB	chr4:74757657-74758055	IMR90	lung:	n/a	n/a
18	CEBPB	chr4:74766935-74767258	K562	blood:	n/a	chr4:74767079-74767088 chr4:74767078-74767089
19	CEBPB	chr4:74766916-74767226	K562	blood:	n/a	chr4:74767079-74767088 chr4:74767078-74767089
20	CEBPB	chr4:74770375-74770569	IMR90	lung:	n/a	chr4:74770486-74770499
21	CEBPB	chr4:74757791-74757829	HepG2	liver:	n/a	n/a
22	CEBPB	chr4:74736004-74736364	HepG2	liver:	n/a	chr4:74736180-74736193 chr4:74736180-74736191 chr4:74736181-74736192 chr4:74736180-74736193 chr4:74736182-74736191
23	CEBPB	chr4:74736042-74736299	MCF-7	breast:	n/a	chr4:74736180-74736193 chr4:74736180-74736191 chr4:74736181-74736192 chr4:74736180-74736193 chr4:74736182-74736191
24	CEBPB	chr4:74730781-74730898	K562	blood:	n/a	n/a
25	CEBPB	chr4:74767028-74767140	H1-hESC	embryonic stem cell:	n/a	chr4:74767079-74767088 chr4:74767078-74767089
26	CEBPB	chr4:74736082-74736243	K562	blood:	n/a	chr4:74736180-74736193 chr4:74736180-74736191 chr4:74736181-74736192 chr4:74736180-74736193 chr4:74736182-74736191
27	CEBPB	chr4:74766934-74767225	HepG2	liver:	n/a	chr4:74767079-74767088 chr4:74767078-74767089
28	CEBPB	chr4:74757611-74758040	A549	lung:	n/a	n/a
29	CEBPB	chr4:74736035-74736342	Hela-S3	cervix:	n/a	chr4:74736180-74736193 chr4:74736180-74736191 chr4:74736181-74736192 chr4:74736180-74736193 chr4:74736182-74736191
30	CEBPB	chr4:74770279-74770608	K562	blood:	n/a	chr4:74770486-74770499 chr4:74770354-74770365
31	CEBPB	chr4:74766974-74767139	A549	lung:	n/a	chr4:74767079-74767088 chr4:74767078-74767089
32	CEBPB	chr4:74757649-74758026	Hela-S3	cervix:	n/a	n/a
33	CEBPB	chr4:74751588-74751948	Hela-S3	cervix:	n/a	n/a
34	CEBPB	chr4:74770238-74770583	K562	blood:	n/a	chr4:74770486-74770499 chr4:74770354-74770365
35	CEBPB	chr4:74730266-74730313	Hela-S3	cervix:	n/a	n/a
36	CEBPB	chr4:74770354-74770576	A549	lung:	n/a	chr4:74770486-74770499 chr4:74770354-74770365
37	CEBPB	chr4:74736012-74736326	ECC-1	luminal epithelium:	n/a	chr4:74736180-74736193 chr4:74736180-74736191 chr4:74736181-74736192 chr4:74736180-74736193 chr4:74736182-74736191
38	CEBPB	chr4:74736021-74736362	IMR90	lung:	n/a	chr4:74736180-74736193 chr4:74736180-74736191 chr4:74736181-74736192 chr4:74736180-74736193 chr4:74736182-74736191
39	CEBPB	chr4:74736012-74736378	K562	blood:	n/a	chr4:74736180-74736193 chr4:74736180-74736191 chr4:74736181-74736192 chr4:74736180-74736193 chr4:74736182-74736191
40	CEBPB	chr4:74735973-74736321	ECC-1	luminal epithelium:	n/a	chr4:74736180-74736193 chr4:74736180-74736191 chr4:74736181-74736192 chr4:74736180-74736193 chr4:74736182-74736191
41	CEBPB	chr4:74770358-74770582	K562	blood:	n/a	chr4:74770486-74770499
42	CEBPB	chr4:74766914-74767213	IMR90	lung:	n/a	chr4:74767079-74767088 chr4:74767078-74767089
43	CEBPB	chr4:74735955-74736311	A549	lung:	n/a	chr4:74736180-74736193 chr4:74736180-74736191 chr4:74736181-74736192 chr4:74736180-74736193 chr4:74736182-74736191
44	CEBPB	chr4:74757651-74757991	A549	lung:	n/a	n/a
45	CEBPB	chr4:74736000-74736362	H1-hESC	embryonic stem cell:	n/a	chr4:74736180-74736193 chr4:74736180-74736191 chr4:74736181-74736192 chr4:74736180-74736193 chr4:74736182-74736191
46	CEBPB	chr4:74766310-74766422	HepG2	liver:	n/a	n/a
47	CEBPB	chr4:74757515-74758136	A549	lung:	n/a	n/a
48	CEBPB	chr4:74736002-74736373	A549	lung:	n/a	chr4:74736180-74736193 chr4:74736180-74736191 chr4:74736181-74736192 chr4:74736180-74736193 chr4:74736182-74736191
49	CEBPB	chr4:74735981-74736334	K562	blood:	n/a	chr4:74736180-74736193 chr4:74736180-74736191 chr4:74736181-74736192 chr4:74736180-74736193 chr4:74736182-74736191
50	CEBPB	chr4:74735918-74736474	A549	lung:	n/a	chr4:74736180-74736193 chr4:74736180-74736191 chr4:74736181-74736192 chr4:74736180-74736193 chr4:74736182-74736191

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:74735924-74735974	GM19239	blood:	n/a
2	chr4:74734924-74734974	BE2_C	brain:	n/a
3	chr4:74734924-74734974	ProgFib	skin:	n/a
4	chr4:74738902-74738952	HL-60	blood:	n/a
5	chr4:74731300-74731350	NT2-D1	testis:	n/a
6	chr4:74734874-74734924	IMR90	lung:	fetal
7	chr4:74734919-74734969	PFSK-1	brain:	n/a
8	chr4:74734762-74734812	AoSMC	blood vessel:	n/a
9	chr4:74734762-74734812	BE2_C	brain:	n/a
10	chr4:74734874-74734924	GM12892	blood:	n/a
11	chr4:74734919-74734969	HIPEpiC	eye:	n/a
12	chr4:74735092-74735142	HRCEpiC	kidney:	n/a
13	chr4:74735149-74735199	Hela-S3	cervix:	n/a
14	chr4:74735149-74735199	HL-60	blood:	n/a
15	chr4:74734762-74734812	ProgFib	skin:	n/a
16	chr4:74759644-74759694	HUVEC	blood vessel:	n/a
17	chr4:74735092-74735142	AG04450	lung:	fetal
18	chr4:74735468-74735518	Hela-S3	cervix:	n/a
19	chr4:74735149-74735199	HepG2	liver:	n/a
20	chr4:74734874-74734924	NHBE	bronchial:	n/a
21	chr4:74759644-74759694	HRE	kidney:	n/a
22	chr4:74735101-74735151	SK-N-MC	brain:	n/a
23	chr4:74735149-74735199	AG09319	gingival:	n/a
24	chr4:74738902-74738952	BE2_C	brain:	n/a
25	chr4:74735924-74735974	NB4	blood:	n/a
26	chr4:74735468-74735518	HRE	kidney:	n/a
27	chr4:74735056-74735106	ECC-1	luminal epithelium:	n/a
28	chr4:74734762-74734812	SK-N-SH	brain:	n/a
29	chr4:74731300-74731350	Jurkat	blood:	n/a
30	chr4:74738902-74738952	HPAEpiC	pulmonary alveolar:	n/a
31	chr4:74735092-74735142	Hepatocyte	liver:	n/a
32	chr4:74735468-74735518	IMR90	lung:	fetal
33	chr4:74735924-74735974	SKMC	muscle:	n/a
34	chr4:74759644-74759694	MCF-7	breast:	n/a
35	chr4:74735149-74735199	NHBE	bronchial:	n/a
36	chr4:74735030-74735080	HCT-116	colon:	n/a
37	chr4:74735924-74735974	MCF10A-Er-Src	breast:	n/a
38	chr4:74731300-74731350	NH-A	brain:	n/a
39	chr4:74738902-74738952	Jurkat	blood:	n/a
40	chr4:74734714-74734764	HMEC	breast:	n/a
41	chr4:74738902-74738952	K562	blood:	n/a
42	chr4:74735030-74735080	MCF10A-Er-Src	breast:	n/a
43	chr4:74734762-74734812	HUVEC	blood vessel:	n/a
44	chr4:74735924-74735974	MCF-7	breast:	n/a
45	chr4:74734714-74734764	SK-N-SH	brain:	n/a
46	chr4:74759644-74759694	BJ	skin:	n/a
47	chr4:74734919-74734969	NHBE	bronchial:	n/a
48	chr4:74731300-74731350	IMR90	lung:	fetal
49	chr4:74734919-74734969	SK-N-MC	brain:	n/a
50	chr4:74735101-74735151	HRPEpiC	eye:	n/a

No.	Distal block	Cell Line	Cell type
1	chr4:74746413..74748003-chr4:74754360..74756735,2	K562	blood:
2	chr4:74726785..74728878-chr4:74730799..74732638,2	MCF-7	breast:
3	chr4:74758611..74762453-chr4:74763527..74766152,5	K562	blood:
4	chr4:74528321..74529495-chr4:74729762..74730750,4	MCF-7	breast:
5	chr4:74717554..74719920-chr4:74738464..74740646,2	K562	blood:
6	chr4:74710377..74712305-chr4:74732116..74734240,2	K562	blood:
7	chr4:74759338..74760983-chr4:74763696..74765672,2	K562	blood:
8	chr4:74718960..74724397-chr4:74728393..74732828,5	K562	blood:
9	chr4:74746413..74748003-chr4:74754360..74756735,2	K562	blood:
10	chr4:74726785..74728878-chr4:74730799..74732638,2	MCF-7	breast:
11	chr4:74733068..74735254-chr4:74743747..74745654,2	K562	blood:
12	chr4:74759338..74760983-chr4:74763696..74765672,2	K562	blood:
13	chr4:74748840..74751609-chr4:74903470..74906256,2	K562	blood:
14	chr4:74736057..74738818-chr4:74920006..74922107,2	MCF-7	breast:
15	chr4:74724927..74730400-chr4:74731637..74736149,6	K562	blood:
16	chr4:74766463..74768421-chr4:74779822..74782631,2	K562	blood:
17	chr4:74528297..74529106-chr4:74730060..74730707,3	K562	blood:
18	chr4:74710805..74713801-chr4:74732116..74734607,2	K562	blood:
19	chr4:74762185..74764051-chr4:74784801..74787079,2	K562	blood:
20	chr4:74528090..74529212-chr4:74729841..74730672,4	MCF-7	breast:
21	chr4:74746733..74749613-chr4:74751019..74753569,2	K562	blood:
22	chr4:74764548..74766659-chr4:74904527..74906987,2	K562	blood:
23	chr4:74718960..74724397-chr4:74728393..74732828,5	K562	blood:
24	chr4:74719674..74726110-chr4:74728599..74734688,9	K562	blood:
25	chr4:74719674..74726110-chr4:74728599..74734688,9	K562	blood:
26	chr4:74758611..74762453-chr4:74763527..74766152,5	K562	blood:
27	chr4:74746733..74749613-chr4:74751019..74753569,2	K562	blood:

Variant related genes	Relation type
CXCL1	TF binding region
CXCL1	CpG island
ENSG00000163734	chromatin interactions
ENSG00000248848	chromatin interactions
ENSG00000163739	chromatin interactions
ENSG00000109272	chromatin interactions
ENSG00000250550	chromatin interactions

Extended variants
information (count: 2123 )
Associated
traits (count: 81 )

Variant overlapped rSNPs/rCNVs (count:2123 , 50 per page) page: 1 2 3 4 5 6 7 ... 43

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7688774	chr4:74723372-74723373	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs561075047	chr4:74723387-74723388	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs115478956	chr4:74723398-74723399	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs540438637	chr4:74723409-74723410	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs371521371	chr4:74723418-74723419	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs548486573	chr4:74723429-74723430	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs144318247	chr4:74723455-74723456	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs116009736	chr4:74723474-74723475	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs72853848	chr4:74723491-74723492	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs183509141	chr4:74723500-74723501	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs148768806	chr4:74723533-74723534	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs567872575	chr4:74723589-74723590	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs534840301	chr4:74723631-74723632	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs546810962	chr4:74723684-74723685	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs143951963	chr4:74723696-74723697	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs62312421	chr4:74723723-74723724	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs78974320	chr4:74723736-74723737	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs189314495	chr4:74723737-74723738	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs535910268	chr4:74723774-74723775	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs4392479	chr4:74723787-74723788	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
21	rs573179580	chr4:74723809-74723810	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
22	rs540402063	chr4:74723834-74723835	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
23	rs565095265	chr4:74723877-74723878	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
24	rs577145528	chr4:74723909-74723910	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
25	rs146872520	chr4:74723927-74723928	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
26	rs563669647	chr4:74723933-74723934	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
27	rs557860283	chr4:74723988-74723989	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
28	rs530891896	chr4:74723989-74723990	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
29	rs139552402	chr4:74724007-74724008	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
30	rs16850099	chr4:74724008-74724009	Weak transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs144185014	chr4:74724044-74724045	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
32	rs543052348	chr4:74724100-74724101	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
33	rs151069101	chr4:74724120-74724121	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
34	rs114056896	chr4:74724181-74724182	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
35	rs538892112	chr4:74724216-74724217	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs550641811	chr4:74724344-74724345	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs371242448	chr4:74724345-74724346	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs529507131	chr4:74724347-74724348	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs7695276	chr4:74724385-74724386	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs559664170	chr4:74724395-74724396	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs566740485	chr4:74724407-74724408	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs140965901	chr4:74724463-74724464	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs150216622	chr4:74724485-74724486	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs565821193	chr4:74724497-74724498	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs577099887	chr4:74724501-74724502	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs544083543	chr4:74724518-74724519	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs10155486	chr4:74724524-74724525	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs528713974	chr4:74724546-74724547	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs554834249	chr4:74724569-74724570	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs7695652	chr4:74724582-74724583	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:81)

Disease	PMID	Source
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Medulloblastoma	21979893	CNVD
Neuroblastoma	18923191	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21858162	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
lymphocytic leukemia	21291569	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Non-small cell lung cancer	21829676	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	17603634	CNVD
Glioblastoma multiforme	21922591	CNVD
Parkinson disease	21956041	CNVD
Mental retardation	20522426	CNVD
delayed speech	20522426	CNVD
growth disorder	20522426	CNVD
Hepatocellular carcinoma	16750200	CNVD
Myxofibrosarcoma	16751306	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Parkinson disease	18923514	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Cancer	21183584	CNVD
Breast cancer	16272173	CNVD
Colorectal cancer	19359472	CNVD
Malignant mesothelioma	18160781	CNVD
Medulloblastoma	18056178	CNVD
Multiple myeloma	17077331	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Oral squamous cell carcinoma	17134496	CNVD
4q-syndrome	17576883	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Muscular dystrophy	21149563	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Cervical cancer	21062161	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	16608533	CNVD
Colorectal cancer	16272173	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Lung cancer	19208797	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21785460	CNVD
Prostate cancer	16573809	CNVD
Osteoporosis	18992858	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Myelodysplastic syndrome	21251322	CNVD
Multiple myeloma	17550852	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Myelofibrosis	22110671	CNVD
Abnormal phenotypes	18644119	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Cancer	22429812	CNVD
Intracranial aneurysm	16715129	CNVD
Multiple myeloma	16616336	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ovarian cancer	21720365	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	20932292	CNVD
Pancreatic cancer	17952125	CNVD
Renal cell carcinoma	20952505	CNVD

Chromatin state (count:721 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:74719400-74727800	Weak transcription	NHLF	lung
2	chr4:74719400-74733600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
3	chr4:74719600-74724800	Weak transcription	Right Atrium	heart
4	chr4:74719800-74723400	Weak transcription	Pancreas	Pancrea
5	chr4:74721400-74726000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
6	chr4:74721400-74729200	Weak transcription	Primary neutrophils fromperipheralblood	blood
7	chr4:74722200-74725000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
8	chr4:74722600-74724200	ZNF genes & repeats	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
9	chr4:74722800-74723800	ZNF genes & repeats	Muscle Satellite Cultured Cells	--
10	chr4:74722800-74724800	Weak transcription	Osteobl	bone
11	chr4:74723000-74728000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
12	chr4:74723200-74723600	Enhancers	Monocytes-CD14+_RO01746	blood
13	chr4:74723200-74723800	Enhancers	Fetal Kidney	kidney
14	chr4:74723200-74725200	Weak transcription	Liver	Liver
15	chr4:74723400-74723600	Enhancers	Primary monocytes fromperipheralblood	blood
16	chr4:74723400-74723600	Enhancers	Pancreas	Pancrea
17	chr4:74723800-74724400	Weak transcription	Fetal Kidney	kidney
18	chr4:74723800-74725200	Weak transcription	Muscle Satellite Cultured Cells	--
19	chr4:74724200-74730600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
20	chr4:74724400-74726600	Enhancers	Fetal Kidney	kidney
21	chr4:74724600-74725400	Enhancers	Dnd41	blood
22	chr4:74724600-74725800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
23	chr4:74724600-74726200	Enhancers	Fetal Lung	lung
24	chr4:74724800-74725000	Enhancers	Right Atrium	heart
25	chr4:74724800-74725600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
26	chr4:74724800-74725600	Enhancers	Fetal Stomach	stomach
27	chr4:74724800-74726000	Enhancers	NH-A	brain
28	chr4:74724800-74726800	Enhancers	Osteobl	bone
29	chr4:74724800-74727000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
30	chr4:74725000-74725400	Enhancers	Primary hematopoietic stem cells short term culture	blood
31	chr4:74725000-74726000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
32	chr4:74725200-74725800	Enhancers	Liver	Liver
33	chr4:74725200-74726000	Enhancers	Muscle Satellite Cultured Cells	--
34	chr4:74725600-74726000	Enhancers	HSMM	muscle
35	chr4:74725600-74726200	Enhancers	Rectal Mucosa Donor 31	rectum
36	chr4:74725800-74726200	Enhancers	Fetal Brain Female	brain
37	chr4:74726000-74726200	Enhancers	NHDF-Ad	bronchial
38	chr4:74726000-74726400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
39	chr4:74726000-74726400	Enhancers	Pancreatic Islets	Pancreatic Islet
40	chr4:74726000-74727800	Weak transcription	Muscle Satellite Cultured Cells	--
41	chr4:74726000-74728000	Weak transcription	NH-A	brain
42	chr4:74726000-74734200	Weak transcription	HSMM	muscle
43	chr4:74726200-74733600	Weak transcription	NHDF-Ad	bronchial
44	chr4:74726400-74727800	Weak transcription	Pancreatic Islets	Pancreatic Islet
45	chr4:74726400-74733800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
46	chr4:74726800-74727800	Weak transcription	Osteobl	bone
47	chr4:74727000-74728000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
48	chr4:74727800-74728000	Enhancers	Pancreatic Islets	Pancreatic Islet
49	chr4:74727800-74728200	Enhancers	NHLF	lung
50	chr4:74727800-74728400	Enhancers	Osteobl	bone

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