Variant report

Variant	esv2761140
Chromosome Location	chr7:5824725-5868561
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:988)
CpG islands
(count:1282)
Chromatin interactive
region (count:5)
LncRNA
region (count:10)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:988 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:5867592-5867694	HepG2	liver:	n/a	n/a
2	ARID3A	chr7:5837477-5837688	K562	blood:	n/a	n/a
3	ARID3A	chr7:5826122-5826510	K562	blood:	n/a	n/a
4	ARID3A	chr7:5862528-5862814	K562	blood:	n/a	n/a
5	ARID3A	chr7:5862273-5862605	HepG2	liver:	n/a	n/a
6	ARID3A	chr7:5867459-5867694	K562	blood:	n/a	n/a
7	ATF1	chr7:5837427-5837729	K562	blood:	n/a	n/a
8	ATF1	chr7:5862457-5862892	K562	blood:	n/a	n/a
9	ATF1	chr7:5826182-5826466	K562	blood:	n/a	n/a
10	ATF2	chr7:5862327-5862966	GM12878	blood:	n/a	n/a
11	ATF2	chr7:5862306-5862777	H1-hESC	embryonic stem cell:	n/a	n/a
12	ATF2	chr7:5862330-5862768	H1-hESC	embryonic stem cell:	n/a	n/a
13	ATF2	chr7:5862355-5862904	GM12878	blood:	n/a	n/a
14	ATF3	chr7:5862411-5862898	H1-hESC	embryonic stem cell:	n/a	n/a
15	ATF3	chr7:5862635-5862799	GM12878	blood:	n/a	n/a
16	ATF3	chr7:5862558-5862865	H1-hESC	embryonic stem cell:	n/a	n/a
17	ATF3	chr7:5862563-5862853	HepG2	liver:	n/a	n/a
18	ATF3	chr7:5862421-5862902	HepG2	liver:	n/a	n/a
19	ATF3	chr7:5826108-5826365	K562	blood:	n/a	n/a
20	ATF3	chr7:5862540-5862867	K562	blood:	n/a	n/a
21	ATF3	chr7:5826145-5826345	K562	blood:	n/a	n/a
22	ATF3	chr7:5862384-5862926	GM12878	blood:	n/a	n/a
23	BCLAF1	chr7:5862267-5862957	GM12878	blood:	n/a	n/a
24	BHLHE40	chr7:5862309-5862995	GM12878	blood:	n/a	n/a
25	BHLHE40	chr7:5862470-5862879	HepG2	liver:	n/a	n/a
26	BHLHE40	chr7:5826102-5826422	K562	blood:	n/a	n/a
27	BHLHE40	chr7:5862350-5862941	K562	blood:	n/a	n/a
28	BHLHE40	chr7:5830403-5830547	A549	lung:	n/a	n/a
29	BRCA1	chr7:5862392-5862880	Hela-S3	cervix:	n/a	n/a
30	CBX3	chr7:5862122-5862937	K562	blood:	n/a	n/a
31	CBX3	chr7:5825939-5826501	K562	blood:	n/a	n/a
32	CBX3	chr7:5862294-5862858	K562	blood:	n/a	n/a
33	CCNT2	chr7:5862562-5862965	K562	blood:	n/a	n/a
34	CEBPB	chr7:5826040-5826457	K562	blood:	n/a	n/a
35	CEBPB	chr7:5862300-5862905	Hela-S3	cervix:	n/a	n/a
36	CEBPB	chr7:5857273-5857447	K562	blood:	n/a	n/a
37	CEBPB	chr7:5862463-5862811	K562	blood:	n/a	n/a
38	CEBPB	chr7:5862485-5862785	H1-hESC	embryonic stem cell:	n/a	n/a
39	CEBPB	chr7:5826224-5826396	K562	blood:	n/a	n/a
40	CEBPB	chr7:5862485-5862789	HepG2	liver:	n/a	n/a
41	CEBPB	chr7:5826163-5826405	Hela-S3	cervix:	n/a	n/a
42	CHD1	chr7:5862335-5862830	GM12878	blood:	n/a	n/a
43	CHD2	chr7:5862568-5862938	K562	blood:	n/a	n/a
44	CHD2	chr7:5862510-5862960	Hela-S3	cervix:	n/a	n/a
45	CHD2	chr7:5862517-5862845	H1-hESC	embryonic stem cell:	n/a	n/a
46	CHD2	chr7:5862475-5862938	GM12878	blood:	n/a	n/a
47	CREB1	chr7:5862210-5863144	HepG2	liver:	n/a	n/a
48	CREB1	chr7:5862382-5863056	H1-hESC	embryonic stem cell:	n/a	n/a
49	CREB1	chr7:5862540-5862995	H1-hESC	embryonic stem cell:	n/a	n/a
50	CREB1	chr7:5862499-5862980	A549	lung:	n/a	n/a

(count:1282 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:5862839-5862889	HCPEpiC	choroid plexus:	n/a
2	chr7:5862839-5862889	HCPEpiC	choroid plexus:	n/a
3	chr7:5862449-5862499	HAEpiC	amniotic membrane:	n/a
4	chr7:5863510-5863560	Jurkat	blood:	n/a
5	chr7:5833275-5833325	Hela-S3	cervix:	n/a
6	chr7:5862754-5862804	NH-A	brain:	n/a
7	chr7:5862983-5863033	LNCaP	prostate:	n/a
8	chr7:5862839-5862889	HMEC	breast:	n/a
9	chr7:5834372-5834422	LNCaP	prostate:	n/a
10	chr7:5834292-5834342	PFSK-1	brain:	n/a
11	chr7:5862839-5862889	H1-hESC	embryonic stem cell:	embryo
12	chr7:5834372-5834422	NHBE	bronchial:	n/a
13	chr7:5862754-5862804	Hepatocyte	liver:	n/a
14	chr7:5834292-5834342	HL-60	blood:	n/a
15	chr7:5862754-5862804	HepG2	liver:	n/a
16	chr7:5865915-5865965	SAEC	small airway:	n/a
17	chr7:5833444-5833494	HPAEpiC	pulmonary alveolar:	n/a
18	chr7:5862754-5862804	GM12878	blood:	n/a
19	chr7:5865915-5865965	HCPEpiC	choroid plexus:	n/a
20	chr7:5862839-5862889	SK-N-SH_RA	brain:	n/a
21	chr7:5834425-5834475	SK-N-MC	brain:	n/a
22	chr7:5859245-5859295	HCM	heart:	n/a
23	chr7:5862983-5863033	AG04449	skin:	fetal
24	chr7:5833444-5833494	U87	brain:	n/a
25	chr7:5859245-5859295	SKMC	muscle:	n/a
26	chr7:5863510-5863560	HCT-116	colon:	n/a
27	chr7:5862661-5862711	ovcar-3	ovarian:	n/a
28	chr7:5862740-5862790	HL-60	blood:	n/a
29	chr7:5862839-5862889	NHDF-neo	bronchial:	n/a
30	chr7:5862996-5863046	HL-60	blood:	n/a
31	chr7:5833383-5833433	ECC-1	luminal epithelium:	n/a
32	chr7:5862451-5862501	AG09309	skin:	n/a
33	chr7:5833275-5833325	H1-hESC	embryonic stem cell:	embryo
34	chr7:5862839-5862889	IMR90	lung:	fetal
35	chr7:5862661-5862711	SK-N-SH_RA	brain:	n/a
36	chr7:5862658-5862708	ovcar-3	ovarian:	n/a
37	chr7:5862740-5862790	HRPEpiC	eye:	n/a
38	chr7:5862839-5862889	HRE	kidney:	n/a
39	chr7:5862839-5862889	MCF-7	breast:	n/a
40	chr7:5833444-5833494	AoSMC	blood vessel:	n/a
41	chr7:5862658-5862708	BE2_C	brain:	n/a
42	chr7:5863510-5863560	PrEC	prostate:	n/a
43	chr7:5862983-5863033	HCF	heart:	n/a
44	chr7:5862449-5862499	LNCaP	prostate:	n/a
45	chr7:5825437-5825487	HCF	heart:	n/a
46	chr7:5859245-5859295	HCF	heart:	n/a
47	chr7:5862839-5862889	HCM	heart:	n/a
48	chr7:5859245-5859295	HNPCEpiC	eye:	n/a
49	chr7:5834292-5834342	T-47D	breast:	n/a
50	chr7:5833383-5833433	ovcar-3	ovarian:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr7:5464152..5466960-chr7:5862123..5864390,2	MCF-7	breast:
2	chr7:5195253..5196797-chr7:5849975..5851503,2	MCF-7	breast:
3	chr7:5198471..5200829-chr7:5846767..5848341,2	MCF-7	breast:
4	chr7:5866466..5869217-chr7:5871734..5873608,2	MCF-7	breast:
5	chr3:107149613..107150322-chr7:5862636..5863385,2	NB4	blood:

(count:10 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-OCM-3	chr7:5862823-5863157	NONHSAT118944
2	lnc-OCM-1	chr7:5850594-5850617	XLOC_005976
3	lnc-OCM-3	chr7:5862820-5863157	NONHSAT118942
4	lnc-OCM-1	chr7:5850593-5850617	NONHSAT118937
5	lnc-OCM-1	chr7:5855828-5855979	NONHSAT118937
6	lnc-OCM-1	chr7:5834113-5834518	XLOC_005976
7	lnc-OCM-3	chr7:5862875-5863157	NONHSAT118948
8	lnc-OCM-1	chr7:5834113-5834518	XLOC_005976
9	lnc-OCM-1	chr7:5834112-5834518	NONHSAT118937
10	lnc-OCM-1	chr7:5855829-5855979	XLOC_005976

No data

Variant related genes	Relation type
RNF216	TF binding region
ZNF815P	TF binding region
RNF216	CpG island
ZNF815P	CpG island
ENSG00000182095	chromatin interactions
ENSG00000273125	chromatin interactions
ENSG00000272953	chromatin interactions
NR3C1	miRNA target sites

Extended variants
information (count: 2400 )
Associated
traits (count: 79 )

Variant overlapped rSNPs/rCNVs (count:2400 , 50 per page) page: 1 2 3 4 5 6 7 ... 48

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs535475892	chr7:5824735-5824736	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs192766129	chr7:5824746-5824747	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs548154997	chr7:5824749-5824750	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs140821511	chr7:5824767-5824768	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs184326832	chr7:5824808-5824809	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs376629713	chr7:5824822-5824823	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs549708879	chr7:5824856-5824857	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs369545329	chr7:5824872-5824873	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs568594245	chr7:5824875-5824876	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs535933433	chr7:5824887-5824888	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs569738426	chr7:5824892-5824893	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs55921139	chr7:5824912-5824913	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs547874948	chr7:5824916-5824917	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs66467570	chr7:5824949-5824950	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs539402918	chr7:5824962-5824963	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs558436030	chr7:5825109-5825110	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs189619273	chr7:5825112-5825113	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs543621052	chr7:5825124-5825125	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs78722803	chr7:5825147-5825148	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs144570342	chr7:5825164-5825165	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs541548086	chr7:5825180-5825181	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs559770326	chr7:5825181-5825182	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs572019350	chr7:5825192-5825193	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs374886746	chr7:5825197-5825198	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs60979660	chr7:5825220-5825221	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs35604390	chr7:5825238-5825239	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs57360471	chr7:5825259-5825260	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs61441466	chr7:5825269-5825270	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs540991192	chr7:5825300-5825301	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs559256395	chr7:5825319-5825320	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs550032584	chr7:5825345-5825346	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs13241044	chr7:5825365-5825366	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs111628473	chr7:5825381-5825382	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs77474987	chr7:5825387-5825388	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs565999160	chr7:5825412-5825413	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs533403921	chr7:5825437-5825438	Weak transcription	CpG island	1 gene(s)	Overlapped CNVs	n/a
37	rs530551619	chr7:5825513-5825514	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs570362771	chr7:5825545-5825546	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs181950319	chr7:5825551-5825552	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs568582809	chr7:5825561-5825562	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs28580503	chr7:5825588-5825589	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs534850590	chr7:5825646-5825647	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs60549775	chr7:5825653-5825654	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs572046544	chr7:5825693-5825694	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs545814469	chr7:5825701-5825702	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs71547792	chr7:5825713-5825714	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs35850997	chr7:5825727-5825728	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs186288784	chr7:5825737-5825738	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs557449995	chr7:5825802-5825803	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs4720644	chr7:5825807-5825808	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:79)

Disease	PMID	Source
Lynch syndrome	22585707	CNVD
Follicular lymphoma	20505157	CNVD
Breast cancer	16397240	CNVD
Raine Syndrome	17924334	CNVD
Diffuse large b-cell lymphoma	21266526	CNVD
Melanoma	18172304	CNVD
Sudden cardiac death	19188705	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	16573809	CNVD
Glioma	18556773	CNVD
Ovarian cancer	21720365	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Ovarian cancer	22174824	CNVD
Urothelial carcinoma	18382360	CNVD
Medulloblastoma	21979893	CNVD
Lynch syndrome	18415027	CNVD
Biliary cancer	19435499	CNVD
Cancer	16751803	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Wilms tumour	21544195	CNVD
Glioblastoma multiforme	17387387	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	18923191	CNVD
Glioma	21971842	CNVD
Glioblastoma multiforme	21080181	CNVD
Liposarcoma	21253554	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
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
Developmental delay	21147756	CNVD
Prostate cancer	18632612	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21364760	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Leukemia	23979775	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Urothelial carcinoma	21177765	CNVD
Bladder cancer	21909424	CNVD
Myelofibrosis	22110671	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	21045282	CNVD
Disorders of sex development	21048976	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Schizophrenia	21346763	CNVD
Acute myeloid leukemia	21251322	CNVD
Pancreatic cancer	17952125	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:573 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:5821600-5833000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr7:5821800-5826200	Weak transcription	Muscle Satellite Cultured Cells	--
3	chr7:5821800-5826200	Weak transcription	A549	lung
4	chr7:5821800-5826200	Weak transcription	Hela-S3	cervix
5	chr7:5821800-5826200	Weak transcription	K562	blood
6	chr7:5821800-5826400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
7	chr7:5821800-5826400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
8	chr7:5826200-5826600	Enhancers	Muscle Satellite Cultured Cells	--
9	chr7:5826200-5826600	Enhancers	A549	lung
10	chr7:5826200-5826600	Flanking Active TSS	K562	blood
11	chr7:5826200-5826800	Enhancers	Hela-S3	cervix
12	chr7:5826400-5826800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
13	chr7:5826400-5826800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
14	chr7:5826600-5826800	Enhancers	K562	blood
15	chr7:5826800-5831800	Weak transcription	K562	blood
16	chr7:5830800-5831200	Enhancers	Primary neutrophils fromperipheralblood	blood
17	chr7:5831800-5832200	Enhancers	K562	blood
18	chr7:5832200-5835400	Weak transcription	K562	blood
19	chr7:5833000-5833600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
20	chr7:5833600-5836400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
21	chr7:5835200-5836000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
22	chr7:5835400-5835800	Enhancers	ES-I3 Cell Line	embryonic stem cell
23	chr7:5835400-5835800	Enhancers	HUES48 Cell Line	embryonic stem cell
24	chr7:5835400-5835800	Enhancers	iPS-20b Cell Line	embryonic stem cell
25	chr7:5835400-5836000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
26	chr7:5835400-5836200	Enhancers	HepG2	liver
27	chr7:5835400-5838000	Enhancers	K562	blood
28	chr7:5836400-5836600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
29	chr7:5836400-5837600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
30	chr7:5836400-5837800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
31	chr7:5837200-5837800	Enhancers	Primary T cells fromperipheralblood	blood
32	chr7:5837200-5838000	Enhancers	Primary hematopoietic stem cells short term culture	blood
33	chr7:5837200-5838200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
34	chr7:5837400-5837800	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
35	chr7:5841400-5849800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
36	chr7:5842400-5843600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr7:5842600-5843200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
38	chr7:5843000-5844200	Enhancers	Cortex derived primary cultured neurospheres	brain
39	chr7:5843200-5843600	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
40	chr7:5843600-5844200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
41	chr7:5843600-5844600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr7:5844800-5845000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
43	chr7:5847800-5848200	Enhancers	HepG2	liver
44	chr7:5848200-5849200	Weak transcription	HepG2	liver
45	chr7:5849200-5850000	Enhancers	HepG2	liver
46	chr7:5849600-5850600	Enhancers	Brain Germinal Matrix	brain
47	chr7:5849800-5851200	Enhancers	Fetal Brain Male	brain
48	chr7:5850200-5850400	Enhancers	K562	blood
49	chr7:5850200-5851400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
50	chr7:5850400-5851000	Weak transcription	K562	blood

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