Variant report

Variant	nsv608343
Chromosome Location	chr7:124610346-124674022
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:472)
CpG islands
(count:122)
Chromatin interactive
region (count:18)
LncRNA
region (count:14)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:472 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:124656923-124656953	K562	blood:	n/a	n/a
2	ARID3A	chr7:124632397-124633404	K562	blood:	n/a	n/a
3	ARID3A	chr7:124637007-124637167	K562	blood:	n/a	n/a
4	ATF1	chr7:124632844-124633185	K562	blood:	n/a	n/a
5	ATF3	chr7:124632775-124633232	K562	blood:	n/a	n/a
6	BACH1	chr7:124632839-124633414	K562	blood:	n/a	n/a
7	BACH1	chr7:124632210-124632237	K562	blood:	n/a	n/a
8	BHLHE40	chr7:124644549-124644599	K562	blood:	n/a	n/a
9	BHLHE40	chr7:124632911-124633233	K562	blood:	n/a	n/a
10	CBX3	chr7:124632774-124633230	K562	blood:	n/a	n/a
11	CCNT2	chr7:124632875-124633179	K562	blood:	n/a	n/a
12	CEBPB	chr7:124632786-124633289	K562	blood:	n/a	n/a
13	CEBPB	chr7:124632741-124633509	Hela-S3	cervix:	n/a	n/a
14	CEBPB	chr7:124665488-124665855	HepG2	liver:	n/a	n/a
15	CEBPB	chr7:124632813-124633472	IMR90	lung:	n/a	n/a
16	CEBPB	chr7:124632731-124633255	MCF-7	breast:	n/a	n/a
17	CEBPB	chr7:124632938-124633193	K562	blood:	n/a	n/a
18	CEBPB	chr7:124641115-124641235	K562	blood:	n/a	n/a
19	CEBPB	chr7:124632893-124633288	K562	blood:	n/a	n/a
20	CEBPB	chr7:124663957-124664143	K562	blood:	n/a	n/a
21	CEBPB	chr7:124632819-124633342	MCF-7	breast:	n/a	n/a
22	CHD2	chr7:124632838-124633185	Hela-S3	cervix:	n/a	n/a
23	CTCF	chr7:124637040-124637190	GM12864	blood:	n/a	n/a
24	CTCF	chr7:124671020-124671170	GM12866	blood:	n/a	n/a
25	CTCF	chr7:124637040-124637190	GM12869	blood:	n/a	n/a
26	CTCF	chr7:124637102-124637112	GM13976	blood:	n/a	n/a
27	CTCF	chr7:124669020-124669170	AoAF	blood vessel:	n/a	n/a
28	CTCF	chr7:124669020-124669170	HPAF	blood vessel:	n/a	n/a
29	CTCF	chr7:124669020-124669170	HEK293	kidney:	n/a	n/a
30	CTCF	chr7:124637040-124637190	HA-sp	spinal cord:	n/a	n/a
31	CTCF	chr7:124673698-124673861	A549	lung:	n/a	n/a
32	CTCF	chr7:124673720-124673870	WERI-Rb-1	eye:	n/a	n/a
33	CTCF	chr7:124662680-124662830	GM12864	blood:	n/a	n/a
34	CTCF	chr7:124637020-124637170	GM12874	blood:	n/a	n/a
35	CTCF	chr7:124673720-124673881	GM12892	blood:	n/a	n/a
36	CTCF	chr7:124673713-124673867	K562	blood:	n/a	n/a
37	CTCF	chr7:124637060-124637210	GM12865	blood:	n/a	n/a
38	CTCF	chr7:124669000-124669150	GM12873	blood:	n/a	n/a
39	CTCF	chr7:124637200-124637350	HCM	heart:	n/a	n/a
40	CTCF	chr7:124637060-124637210	HPF	lung:	n/a	n/a
41	CTCF	chr7:124673700-124673850	SK-N-SH_RA	brain:	n/a	n/a
42	CTCF	chr7:124636887-124637242	MCF-7	breast:	n/a	n/a
43	CTCF	chr7:124668900-124669050	MCF-7	breast:	n/a	n/a
44	CTCF	chr7:124673706-124673889	LNCaP	prostate:	n/a	n/a
45	CTCF	chr7:124632873-124632894	Spleen_OC	spleen:	n/a	n/a
46	CTCF	chr7:124669040-124669129	MCF-7	breast:	n/a	n/a
47	CTCF	chr7:124637060-124637210	HCPEpiC	choroid plexus:	n/a	n/a
48	CTCF	chr7:124637060-124637210	SAEC	small airway:	n/a	n/a
49	CTCF	chr7:124637040-124637190	AoAF	blood vessel:	n/a	n/a
50	CTCF	chr7:124669120-124669270	HCM	heart:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:124633001-124633051	AoSMC	blood vessel:	n/a
2	chr7:124633001-124633051	PFSK-1	brain:	n/a
3	chr7:124633001-124633051	NT2-D1	testis:	n/a
4	chr7:124633001-124633051	AG09309	skin:	n/a
5	chr7:124633001-124633051	GM19239	blood:	n/a
6	chr7:124625362-124625412	HCM	heart:	n/a
7	chr7:124633001-124633051	AG09319	gingival:	n/a
8	chr7:124633001-124633051	AG04450	lung:	fetal
9	chr7:124625362-124625412	PANC-1	pancreas:	n/a
10	chr7:124625362-124625412	AG09309	skin:	n/a
11	chr7:124633001-124633051	Caco-2	colon:	n/a
12	chr7:124633001-124633051	ProgFib	skin:	n/a
13	chr7:124625362-124625412	ProgFib	skin:	n/a
14	chr7:124633001-124633051	HCF	heart:	n/a
15	chr7:124625362-124625412	RPTEC	kidney:	n/a
16	chr7:124633001-124633051	SK-N-MC	brain:	n/a
17	chr7:124633001-124633051	HAEpiC	amniotic membrane:	n/a
18	chr7:124633001-124633051	GM06990	blood:	n/a
19	chr7:124633001-124633051	SK-N-SH_RA	brain:	n/a
20	chr7:124625362-124625412	GM19239	blood:	n/a
21	chr7:124633001-124633051	K562	blood:	n/a
22	chr7:124625362-124625412	HCPEpiC	choroid plexus:	n/a
23	chr7:124625362-124625412	SK-N-SH_RA	brain:	n/a
24	chr7:124633001-124633051	HEEpiC	esophagus:	n/a
25	chr7:124633001-124633051	HNPCEpiC	eye:	n/a
26	chr7:124633001-124633051	Jurkat	blood:	n/a
27	chr7:124633001-124633051	AG10803	skin:	n/a
28	chr7:124633001-124633051	SKMC	muscle:	n/a
29	chr7:124625362-124625412	NHBE	bronchial:	n/a
30	chr7:124625362-124625412	PFSK-1	brain:	n/a
31	chr7:124625362-124625412	ovcar-3	ovarian:	n/a
32	chr7:124633001-124633051	HCT-116	colon:	n/a
33	chr7:124633001-124633051	GM12891	blood:	n/a
34	chr7:124633001-124633051	AG04449	skin:	fetal
35	chr7:124633001-124633051	NB4	blood:	n/a
36	chr7:124625362-124625412	Caco-2	colon:	n/a
37	chr7:124633001-124633051	SAEC	small airway:	n/a
38	chr7:124625362-124625412	HRPEpiC	eye:	n/a
39	chr7:124633001-124633051	T-47D	breast:	n/a
40	chr7:124633001-124633051	HCM	heart:	n/a
41	chr7:124633001-124633051	NHBE	bronchial:	n/a
42	chr7:124633001-124633051	HRE	kidney:	n/a
43	chr7:124633001-124633051	HRPEpiC	eye:	n/a
44	chr7:124625362-124625412	ECC-1	luminal epithelium:	n/a
45	chr7:124633001-124633051	CMK	blood:	n/a
46	chr7:124633001-124633051	Hepatocyte	liver:	n/a
47	chr7:124625362-124625412	MCF10A-Er-Src	breast:	n/a
48	chr7:124625362-124625412	SAEC	small airway:	n/a
49	chr7:124625362-124625412	MCF-7	breast:	n/a
50	chr7:124625362-124625412	H1-hESC	embryonic stem cell:	embryo

(count:18 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:124625632..124627676-chr7:124628734..124631039,2	MCF-7	breast:
2	chr7:124651129..124654102-chr7:124654805..124659375,5	K562	blood:
3	chr7:124625632..124627676-chr7:124628734..124631039,2	MCF-7	breast:
4	chr7:124651129..124654102-chr7:124654805..124659375,5	K562	blood:
5	chr7:124611698..124614462-chr7:124706318..124708451,2	K562	blood:
6	chr7:124652094..124654102-chr7:124655952..124659375,3	K562	blood:
7	chr7:124641428..124646399-chr7:124650390..124654210,4	K562	blood:
8	chr7:124656588..124658906-chr7:124962987..124965229,2	K562	blood:
9	chr7:124570010..124572071-chr7:124632097..124634842,3	MCF-7	breast:
10	chr7:124559307..124561381-chr7:124633111..124635066,2	MCF-7	breast:
11	chr7:124641428..124646399-chr7:124650390..124654210,4	K562	blood:
12	chr7:124568419..124570704-chr7:124629136..124631296,2	MCF-7	breast:
13	chr7:124610367..124612617-chr7:124646921..124649703,2	K562	blood:
14	chr7:124495485..124496005-chr7:124636684..124637532,2	MCF-7	breast:
15	chr7:124606875..124608614-chr7:124609059..124611420,2	MCF-7	breast:
16	chr7:124666403..124669373-chr7:124671418..124674369,2	MCF-7	breast:
17	chr7:124652094..124654102-chr7:124655952..124659375,3	K562	blood:
18	chr7:124610367..124612617-chr7:124646921..124649703,2	K562	blood:

(count:14 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SPAM1-4	chr7:124660387-124660467	ENSG00000224897
2	lnc-SPAM1-4	chr7:124638324-124638458	XLOC_006231
3	lnc-SPAM1-4	chr7:124640736-124641066	ENSG00000224897
4	lnc-SPAM1-4	chr7:124660387-124660467	ENSG00000224897
5	lnc-SPAM1-4	chr7:124660387-124660535	NONHSAT123092
6	lnc-SPAM1-4	chr7:124660387-124660467	ENSG00000224897
7	lnc-SPAM1-4	chr7:124660387-124660467	ENSG00000224897
8	lnc-SPAM1-4	chr7:124633062-124633253	ENSG00000224897
9	lnc-SPAM1-7	chr7:124631917-124632152	NONHSAT123095
10	lnc-SPAM1-7	chr7:124627790-124627842	NONHSAT123095
11	lnc-POT1-3	chr7:124673634-124673820	ucscGeneNc_uc010lky_1
12	lnc-SPAM1-4	chr7:124660387-124660467	ENSG00000224897
13	lnc-POT1-3	chr7:124656869-124658131	ucscGeneNc_uc010lky_1
14	lnc-SPAM1-4	chr7:124640736-124641124	XLOC_006231

No data

Variant related genes	Relation type
POT1-AS1	TF binding region
EEF1GP1	TF binding region
POT1-AS1	CpG island
EEF1GP1	CpG island
ENSG00000186676	chromatin interactions
ENSG00000128513	chromatin interactions
ENSG00000224897	chromatin interactions
SACM1L	miRNA target sites
CA2	miRNA target sites
SPRY2	miRNA target sites
FGL2	miRNA target sites
CKAP5	miRNA target sites
RRBP1	miRNA target sites
IMPA1	miRNA target sites

Extended variants
information (count: 841 )
Associated
traits (count: 86 )

Variant overlapped rSNPs/rCNVs (count:841 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs575167383	chr7:124612440-124612441	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs188947413	chr7:124612448-124612449	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs193072564	chr7:124612449-124612450	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs557222116	chr7:124612454-124612455	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs111413970	chr7:124612498-124612499	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs568196475	chr7:124612506-124612507	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs199954731	chr7:124612517-124612518	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs150291617	chr7:124612519-124612520	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs55830526	chr7:124612520-124612521	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs185274795	chr7:124612521-124612522	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs574309000	chr7:124612543-124612544	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs542830692	chr7:124612609-124612610	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs553502830	chr7:124612668-124612669	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs545616405	chr7:124612686-124612687	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs564187499	chr7:124612687-124612688	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs570308602	chr7:124612698-124612699	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs573373836	chr7:124612719-124612720	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs67652374	chr7:124612721-124612722	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs376003781	chr7:124612751-124612752	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs573094785	chr7:124612776-124612777	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs373203848	chr7:124612787-124612788	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs35361978	chr7:124627837-124627838	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
23	rs560677411	chr7:124629152-124629153	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs529623599	chr7:124629167-124629168	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs113160031	chr7:124629190-124629191	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs186826006	chr7:124629211-124629212	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs528731068	chr7:124629267-124629268	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs138835098	chr7:124629292-124629293	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs573117842	chr7:124629294-124629295	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs57238558	chr7:124629297-124629298	Inactive region	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs73225453	chr7:124629303-124629304	Inactive region	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs540111276	chr7:124629310-124629311	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs551082558	chr7:124629352-124629353	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs73432500	chr7:124629406-124629407	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs536765221	chr7:124629426-124629427	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs553046276	chr7:124629435-124629436	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs573199614	chr7:124629478-124629479	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs181080484	chr7:124629512-124629513	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs185877208	chr7:124629513-124629514	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs78968601	chr7:124629515-124629516	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs189807325	chr7:124629527-124629528	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs6954266	chr7:124629534-124629535	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs372759274	chr7:124629589-124629590	Inactive region	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs532180194	chr7:124629604-124629605	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs544035277	chr7:124629646-124629647	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs560760871	chr7:124629651-124629652	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs182984904	chr7:124629662-124629663	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs10274820	chr7:124629664-124629665	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
49	rs146379474	chr7:124629708-124629709	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs532181612	chr7:124629720-124629721	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:86)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Medulloblastoma	21979893	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
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Squamous cell cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Glioblastoma multiforme	17387387	CNVD
Low-grade fibromyxoid sarcoma	0	CNVD
Oligodendroglial tumors	17285580	CNVD
Endometrial cancer	22040021	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	21264507	CNVD
Shwachman-Diamond syndrome	22934832	CNVD
Colorectal cancer	19359472	CNVD
Cutaneous malignant melanoma	17690212	CNVD
Leukemia	17361228	CNVD
Breast cancer	16461572	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Malignant melanoma	17690212	CNVD
Renal cell carcinoma	18592004	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Multiple myeloma	17550852	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Neurodevelopmental disorder	22521361	CNVD
abortions and stillbirths	19751515	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
Lung cancer	18438408	CNVD
Metanephric adenoma	20802469	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
Myelodysplastic syndrome	21251322	CNVD
Chronic myeloid leukemia	21384125	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
lymphocytic leukemia	21291569	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	16573809	CNVD
Medulloblastoma	16783165	CNVD
Biliary cancer	19435499	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Prostate cancer	23792589	CNVD
Adenocarcinoma	21044232	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Non-small cell lung cancer	19889201	CNVD
Acute myeloid leukemia	18000384	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Metastatic melanoma	18483359	CNVD
Autism	18414403	CNVD
Autism	19401682	CNVD
Autism	19546859	CNVD
Schizophrenia	19546859	CNVD
Tourette syndrome	19546859	CNVD
Melanoma	19188590	CNVD
Hepatocellular carcinoma	16785998	CNVD
Glioblastoma multiforme	18628472	CNVD
Basal cell lymphoma	21115979	CNVD
Breast cancer	21509527	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
small cell lung cancer	20016488	CNVD
Epilepsy	21635232	CNVD
Squamous cell cancer	20885788	CNVD
Myelofibrosis	22110671	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
abnormal development	18461090	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:71 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:124612400-124612800	Enhancers	Cortex derived primary cultured neurospheres	brain
2	chr7:124629600-124632600	Weak transcription	Stomach Mucosa	stomach
3	chr7:124629800-124630400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr7:124630000-124630400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
5	chr7:124630200-124630400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
6	chr7:124630200-124630400	Enhancers	Hela-S3	cervix
7	chr7:124630200-124630600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
8	chr7:124630200-124630600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
9	chr7:124630200-124630600	Enhancers	NH-A	brain
10	chr7:124630400-124632800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
11	chr7:124630400-124633200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
12	chr7:124630600-124631000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
13	chr7:124630600-124631800	Weak transcription	Hela-S3	cervix
14	chr7:124630600-124632200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
15	chr7:124630600-124632400	Weak transcription	NH-A	brain
16	chr7:124631000-124631200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
17	chr7:124631000-124631200	Enhancers	Aorta	Aorta
18	chr7:124631200-124632800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
19	chr7:124631800-124632800	Enhancers	Hela-S3	cervix
20	chr7:124632200-124633200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
21	chr7:124632400-124632800	Enhancers	NH-A	brain
22	chr7:124632600-124633600	Enhancers	Stomach Mucosa	stomach
23	chr7:124632800-124633000	Flanking Active TSS	Hela-S3	cervix
24	chr7:124632800-124633000	Flanking Active TSS	K562	blood
25	chr7:124632800-124633000	Flanking Active TSS	NH-A	brain
26	chr7:124632800-124633200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
27	chr7:124632800-124633200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
28	chr7:124632800-124633200	Enhancers	Osteobl	bone
29	chr7:124632800-124633600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
30	chr7:124632800-124633800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
31	chr7:124632800-124633800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
32	chr7:124632800-124633800	Enhancers	HUVEC	blood vessel
33	chr7:124633000-124633200	Active TSS	K562	blood
34	chr7:124633000-124633400	Active TSS	Hela-S3	cervix
35	chr7:124633000-124633400	Active TSS	NH-A	brain
36	chr7:124633200-124633600	Flanking Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
37	chr7:124633200-124633600	Weak transcription	Aorta	Aorta
38	chr7:124633200-124633600	Flanking Active TSS	K562	blood
39	chr7:124633200-124633600	Active TSS	Osteobl	bone
40	chr7:124633200-124633800	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
41	chr7:124633200-124633800	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
42	chr7:124633200-124634000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
43	chr7:124633200-124634200	Enhancers	Placenta Amnion	Placenta Amnion
44	chr7:124633400-124634000	Flanking Active TSS	Hela-S3	cervix
45	chr7:124633400-124634000	Flanking Active TSS	NH-A	brain
46	chr7:124633600-124633800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
47	chr7:124633600-124633800	Flanking Active TSS	Aorta	Aorta
48	chr7:124633600-124633800	Enhancers	K562	blood
49	chr7:124633600-124634400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
50	chr7:124633800-124634000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow

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