Variant report

Variant	nsv1019021
Chromosome Location	chr7:12310445-12375516
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:656)
CpG islands
(count:122)
Chromatin interactive
region (count:32)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:656 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:12361970-12362233	K562	blood:	n/a	n/a
2	ARID3A	chr7:12361928-12362236	HepG2	liver:	n/a	n/a
3	ATF1	chr7:12360907-12361152	K562	blood:	n/a	n/a
4	BATF	chr7:12362529-12362819	GM12878	blood:	n/a	chr7:12362724-12362735
5	BATF	chr7:12362561-12362908	GM12878	blood:	n/a	chr7:12362724-12362735
6	BCL11A	chr7:12362562-12362789	GM12878	blood:	n/a	n/a
7	BCL11A	chr7:12362543-12362825	GM12878	blood:	n/a	n/a
8	BCL3	chr7:12370808-12371350	K562	blood:	n/a	n/a
9	BHLHE40	chr7:12361210-12361233	K562	blood:	n/a	n/a
10	BHLHE40	chr7:12371392-12371475	A549	lung:	n/a	n/a
11	BHLHE40	chr7:12362651-12362754	GM12878	blood:	n/a	n/a
12	BRCA1	chr7:12310930-12310977	GM12878	blood:	n/a	n/a
13	BRCA1	chr7:12363238-12363314	GM12878	blood:	n/a	n/a
14	CBX3	chr7:12330934-12331289	K562	blood:	n/a	n/a
15	CBX3	chr7:12338999-12339376	K562	blood:	n/a	n/a
16	CCNT2	chr7:12360909-12361396	K562	blood:	n/a	n/a
17	CEBPB	chr7:12357353-12357682	K562	blood:	n/a	chr7:12357510-12357521
18	CEBPB	chr7:12345750-12345982	A549	lung:	n/a	n/a
19	CEBPB	chr7:12365869-12365957	K562	blood:	n/a	chr7:12365903-12365914 chr7:12365903-12365916 chr7:12365903-12365916 chr7:12365903-12365916
20	CEBPB	chr7:12337404-12337716	MCF-7	breast:	n/a	n/a
21	CEBPB	chr7:12357363-12357592	IMR90	lung:	n/a	chr7:12357510-12357521
22	CEBPB	chr7:12360899-12361157	Hela-S3	cervix:	n/a	n/a
23	CEBPB	chr7:12357399-12357607	A549	lung:	n/a	chr7:12357510-12357521
24	CEBPB	chr7:12357429-12357629	HepG2	liver:	n/a	chr7:12357510-12357521
25	CEBPB	chr7:12360962-12361174	K562	blood:	n/a	n/a
26	CEBPB	chr7:12365884-12365914	H1-hESC	embryonic stem cell:	n/a	chr7:12365903-12365914
27	CEBPB	chr7:12341270-12341440	K562	blood:	n/a	n/a
28	CEBPB	chr7:12368645-12369574	H1-hESC	embryonic stem cell:	n/a	n/a
29	CHD2	chr7:12363065-12363428	GM12878	blood:	n/a	n/a
30	CHD2	chr7:12363089-12363397	HepG2	liver:	n/a	n/a
31	CHD2	chr7:12363091-12363608	H1-hESC	embryonic stem cell:	n/a	n/a
32	CTCF	chr7:12331560-12331710	HRPEpiC	eye:	n/a	n/a
33	CTCF	chr7:12331577-12331839	K562	blood:	n/a	n/a
34	CTCF	chr7:12362040-12362190	HFF-Myc	foreskin:	n/a	chr7:12362097-12362118 chr7:12362102-12362120
35	CTCF	chr7:12362100-12362117	A549	lung:	n/a	n/a
36	CTCF	chr7:12362060-12362210	HPF	lung:	n/a	chr7:12362097-12362118 chr7:12362102-12362120
37	CTCF	chr7:12362040-12362190	HPAF	blood vessel:	n/a	chr7:12362097-12362118 chr7:12362102-12362120
38	CTCF	chr7:12361841-12362390	HCT-116	colon:	n/a	chr7:12362097-12362118 chr7:12362102-12362120
39	CTCF	chr7:12331620-12331770	HA-sp	spinal cord:	n/a	n/a
40	CTCF	chr7:12362080-12362230	GM12864	blood:	n/a	chr7:12362097-12362118 chr7:12362102-12362120
41	CTCF	chr7:12331580-12331730	AG10803	skin:	n/a	n/a
42	CTCF	chr7:12331631-12331780	NHEK	skin:	n/a	n/a
43	CTCF	chr7:12331621-12331795	GM10266	blood:	n/a	n/a
44	CTCF	chr7:12331572-12331803	A549	lung:	n/a	n/a
45	CTCF	chr7:12331620-12331770	HPF	lung:	n/a	n/a
46	CTCF	chr7:12362051-12362192	GM13976	blood:	n/a	chr7:12362097-12362118 chr7:12362102-12362120
47	CTCF	chr7:12331551-12331838	H1-hESC	embryonic stem cell:	n/a	n/a
48	CTCF	chr7:12331669-12331778	LNCaP	prostate:	n/a	n/a
49	CTCF	chr7:12331560-12331710	GM12874	blood:	n/a	n/a
50	CTCF	chr7:12331600-12331750	HMEC	breast:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:12363490-12363540	HRCEpiC	kidney:	n/a
2	chr7:12370351-12370401	HPAEpiC	pulmonary alveolar:	n/a
3	chr7:12363490-12363540	SK-N-SH	brain:	n/a
4	chr7:12363490-12363540	A549	lung:	n/a
5	chr7:12370351-12370401	ovcar-3	ovarian:	n/a
6	chr7:12370351-12370401	ProgFib	skin:	n/a
7	chr7:12363490-12363540	ovcar-3	ovarian:	n/a
8	chr7:12363490-12363540	NB4	blood:	n/a
9	chr7:12370351-12370401	Jurkat	blood:	n/a
10	chr7:12370351-12370401	K562	blood:	n/a
11	chr7:12370351-12370401	HRPEpiC	eye:	n/a
12	chr7:12363490-12363540	GM12891	blood:	n/a
13	chr7:12363490-12363540	ProgFib	skin:	n/a
14	chr7:12370351-12370401	SKMC	muscle:	n/a
15	chr7:12363490-12363540	T-47D	breast:	n/a
16	chr7:12363490-12363540	HCT-116	colon:	n/a
17	chr7:12370351-12370401	HEK293	kidney:	embryo
18	chr7:12363490-12363540	HEK293	kidney:	embryo
19	chr7:12363490-12363540	SK-N-MC	brain:	n/a
20	chr7:12370351-12370401	NHDF-neo	bronchial:	n/a
21	chr7:12370351-12370401	AG09309	skin:	n/a
22	chr7:12363490-12363540	SKMC	muscle:	n/a
23	chr7:12370351-12370401	NH-A	brain:	n/a
24	chr7:12363490-12363540	Hela-S3	cervix:	n/a
25	chr7:12363490-12363540	GM19239	blood:	n/a
26	chr7:12363490-12363540	GM06990	blood:	n/a
27	chr7:12363490-12363540	AG09319	gingival:	n/a
28	chr7:12370351-12370401	Hela-S3	cervix:	n/a
29	chr7:12370351-12370401	HCT-116	colon:	n/a
30	chr7:12363490-12363540	HEEpiC	esophagus:	n/a
31	chr7:12363490-12363540	MCF-7	breast:	n/a
32	chr7:12363490-12363540	AG10803	skin:	n/a
33	chr7:12370351-12370401	T-47D	breast:	n/a
34	chr7:12363490-12363540	SK-N-SH_RA	brain:	n/a
35	chr7:12370351-12370401	IMR90	lung:	fetal
36	chr7:12370351-12370401	HCF	heart:	n/a
37	chr7:12363490-12363540	AoSMC	blood vessel:	n/a
38	chr7:12370351-12370401	HL-60	blood:	n/a
39	chr7:12370351-12370401	NHBE	bronchial:	n/a
40	chr7:12370351-12370401	A549	lung:	n/a
41	chr7:12370351-12370401	NB4	blood:	n/a
42	chr7:12370351-12370401	GM06990	blood:	n/a
43	chr7:12363490-12363540	HIPEpiC	eye:	n/a
44	chr7:12370351-12370401	NT2-D1	testis:	n/a
45	chr7:12370351-12370401	HUVEC	blood vessel:	n/a
46	chr7:12370351-12370401	MCF-7	breast:	n/a
47	chr7:12370351-12370401	SK-N-MC	brain:	n/a
48	chr7:12363490-12363540	IMR90	lung:	fetal
49	chr7:12370351-12370401	MCF10A-Er-Src	breast:	n/a
50	chr7:12363490-12363540	ECC-1	luminal epithelium:	n/a

(count:32 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:12333884..12336168-chr7:12337724..12340459,4	K562	blood:
2	chr7:12311161..12313996-chr7:12317609..12319933,2	K562	blood:
3	chr7:12248340..12250610-chr7:12341759..12344659,2	K562	blood:
4	chr7:12249110..12251929-chr7:12341759..12344024,2	K562	blood:
5	chr7:12326033..12327864-chr7:12530775..12532531,2	K562	blood:
6	chr7:12353391..12355072-chr7:12357011..12359494,3	K562	blood:
7	chr7:12353391..12355072-chr7:12357011..12359494,3	K562	blood:
8	chr7:12362078..12365720-chr7:12370304..12373327,3	K562	blood:
9	chr7:12359587..12361942-chr7:12364993..12366787,2	K562	blood:
10	chr7:12362049..12364322-chr7:12365857..12368217,3	K562	blood:
11	chr7:12351255..12355072-chr7:12355211..12359779,5	K562	blood:
12	chr7:12249722..12251364-chr7:12307905..12310601,2	MCF-7	breast:
13	chr7:12362078..12365720-chr7:12370304..12373327,3	K562	blood:
14	chr7:12359587..12361942-chr7:12364993..12366787,2	K562	blood:
15	chr7:12251087..12251775-chr7:12361635..12362202,4	MCF-7	breast:
16	chr7:12359785..12361369-chr7:12363361..12365480,2	K562	blood:
17	chr7:12106833..12107747-chr7:12331137..12332178,5	MCF-7	breast:
18	chr7:12319256..12322046-chr7:12323185..12326325,3	K562	blood:
19	chr7:12359785..12361369-chr7:12363361..12365480,2	K562	blood:
20	chr7:12106923..12107696-chr7:12361667..12362587,3	MCF-7	breast:
21	chr7:12351255..12355072-chr7:12355211..12359779,5	K562	blood:
22	chr7:12365317..12367228-chr7:12375967..12378342,2	K562	blood:
23	chr7:12252737..12254776-chr7:12374517..12377204,2	K562	blood:
24	chr7:12237104..12239270-chr7:12329420..12331412,2	K562	blood:
25	chr7:12311161..12313996-chr7:12317609..12319933,2	K562	blood:
26	chr7:12363684..12366465-chr7:12393124..12396040,2	K562	blood:
27	chr7:12333884..12336168-chr7:12337724..12340459,4	K562	blood:
28	chr7:12319256..12322046-chr7:12323185..12326325,3	K562	blood:
29	chr7:12249029..12251264-chr7:12355308..12358122,2	MCF-7	breast:
30	chr7:12362049..12364322-chr7:12365857..12368217,3	K562	blood:
31	chr7:12356830..12359604-chr7:12404989..12406571,2	K562	blood:
32	chr7:12354059..12356452-chr7:12416852..12418898,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-THSD7A-4	chr7:12370513-12370823	NONHSAT119227
2	lnc-THSD7A-4	chr7:12373091-12373352	NONHSAT119227
3	lnc-VWDE-5	chr7:12360180-12360643	expReg_chr7_1116_-

No data

Variant related genes	Relation type
VWDE	TF binding region
VWDE	CpG island
ENSG00000106460	chromatin interactions

Extended variants
information (count: 2877 )
Associated
traits (count: 92 )

Variant overlapped rSNPs/rCNVs (count:2877 , 50 per page) page: 1 2 3 4 5 6 7 ... 58

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6460910	chr7:12310445-12310446	Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs535831710	chr7:12310450-12310451	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs144216345	chr7:12310473-12310474	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs574653609	chr7:12310485-12310486	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs540416418	chr7:12310496-12310497	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs35044818	chr7:12310497-12310498	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs200369467	chr7:12310543-12310544	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs558635719	chr7:12317809-12317810	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs57964223	chr7:12317817-12317818	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs57694022	chr7:12317836-12317837	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs563569327	chr7:12317857-12317858	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs61054154	chr7:12317859-12317860	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs77559161	chr7:12317863-12317864	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs77553437	chr7:12317867-12317868	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs148593612	chr7:12317871-12317872	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs72584561	chr7:12317890-12317891	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs142974639	chr7:12317900-12317901	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs530525759	chr7:12317915-12317916	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs551020308	chr7:12317941-12317942	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs191868687	chr7:12317956-12317957	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs72584562	chr7:12317972-12317973	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs546765781	chr7:12317981-12317982	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs566630530	chr7:12317989-12317990	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs72584563	chr7:12318004-12318005	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs72584564	chr7:12318023-12318024	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs575594511	chr7:12318038-12318039	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs66601708	chr7:12318039-12318040	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs141356433	chr7:12318043-12318044	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs143752674	chr7:12318044-12318045	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs72584567	chr7:12318094-12318095	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs34091152	chr7:12318098-12318099	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs397977423	chr7:12318102-12318103	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs12674356	chr7:12318115-12318116	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
34	rs572902582	chr7:12318166-12318167	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs72584570	chr7:12318204-12318205	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs564973179	chr7:12318253-12318254	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs530458907	chr7:12318258-12318259	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs34022592	chr7:12318281-12318282	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs549954586	chr7:12318289-12318290	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs550517456	chr7:12318328-12318329	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs561268559	chr7:12318339-12318340	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs67593601	chr7:12318361-12318362	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs113259789	chr7:12318396-12318397	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs546802603	chr7:12318405-12318406	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs12155268	chr7:12318427-12318428	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
46	rs539221137	chr7:12318431-12318432	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs552416646	chr7:12318467-12318468	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs73677581	chr7:12318500-12318501	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs72584572	chr7:12318513-12318514	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs554971192	chr7:12318521-12318522	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:92)

Disease	PMID	Source
Melanoma	18172304	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
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21364760	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Leukemia	23979775	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Autism	22495311	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	16573809	CNVD
Acute myeloid leukemia	21251322	CNVD
Melanoma	17363583	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	16272173	CNVD
Hirschsprung''s Disease	21712996	CNVD
Glioblastoma multiforme	22286061	CNVD
Non-small cell lung cancer	21829676	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Kartagener syndrome	16639409	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Medulloblastoma	17653508	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	19242612	CNVD
Autism	18414403	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	21858162	CNVD
Renal cell carcinoma	18194544	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Autism	22495309	CNVD
Cancer	21637783	CNVD
Squamous cell cancer	20885788	CNVD
Breast cancer	16397240	CNVD
Glioblastoma multiforme	17002787	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Multiple myeloma	17550852	CNVD
Bipolar disorder	19114987	CNVD
Schizophrenia	23813976	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Colorectal cancer	21645411	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:182 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:12308400-12310600	Enhancers	Fetal Intestine Large	intestine
2	chr7:12317800-12318000	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr7:12317800-12318200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
4	chr7:12317800-12318400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr7:12317800-12329400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr7:12323600-12324000	Enhancers	iPS-18 Cell Line	embryonic stem cell
7	chr7:12326800-12327800	Enhancers	Brain Germinal Matrix	brain
8	chr7:12327800-12328600	Weak transcription	Brain Germinal Matrix	brain
9	chr7:12328600-12328800	Enhancers	Brain Germinal Matrix	brain
10	chr7:12329000-12329200	Enhancers	H9 Cell Line	embryonic stem cell
11	chr7:12329200-12330400	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
12	chr7:12329400-12330000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr7:12330200-12330600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
14	chr7:12330400-12331000	Weak transcription	H9 Cell Line	embryonic stem cell
15	chr7:12331000-12331200	ZNF genes & repeats	H9 Cell Line	embryonic stem cell
16	chr7:12331200-12331400	Weak transcription	H9 Cell Line	embryonic stem cell
17	chr7:12331400-12332400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
18	chr7:12334000-12335000	Enhancers	Primary B cells from peripheral blood	blood
19	chr7:12334400-12335000	Enhancers	Primary monocytes fromperipheralblood	blood
20	chr7:12335200-12336200	Enhancers	Breast Myoepithelial Primary Cells	Breast
21	chr7:12335200-12336200	Enhancers	Esophagus	oesophagus
22	chr7:12335200-12338400	Enhancers	Placenta	Placenta
23	chr7:12335600-12336200	Enhancers	NHEK	skin
24	chr7:12335800-12336200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
25	chr7:12335800-12336200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
26	chr7:12335800-12336200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
27	chr7:12335800-12336200	Enhancers	HMEC	breast
28	chr7:12335800-12336400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
29	chr7:12336200-12336400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
30	chr7:12336200-12337200	Weak transcription	NHEK	skin
31	chr7:12336200-12338000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
32	chr7:12336200-12342400	Weak transcription	HMEC	breast
33	chr7:12336400-12337000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
34	chr7:12336400-12337600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
35	chr7:12337000-12337600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
36	chr7:12337000-12337600	Enhancers	Fetal Kidney	kidney
37	chr7:12337000-12338400	Enhancers	iPS-18 Cell Line	embryonic stem cell
38	chr7:12337200-12337600	Enhancers	iPS-20b Cell Line	embryonic stem cell
39	chr7:12337200-12338000	Enhancers	NHEK	skin
40	chr7:12337400-12337800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
41	chr7:12337400-12338600	Enhancers	H1 Cell Line	embryonic stem cell
42	chr7:12337600-12342400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
43	chr7:12337800-12338200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
44	chr7:12338000-12338400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
45	chr7:12338000-12338600	Enhancers	Placenta Amnion	Placenta Amnion
46	chr7:12338000-12342200	Weak transcription	NHEK	skin
47	chr7:12338200-12338400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
48	chr7:12338200-12338800	Enhancers	Adipose Nuclei	Adipose
49	chr7:12338400-12359200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
50	chr7:12339600-12360000	Weak transcription	ES-I3 Cell Line	embryonic stem cell

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