Variant report

Variant	nsv1027152
Chromosome Location	chr7:112631140-112713972
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	ATF1	chr7:112695650-112695833	K562	blood:	n/a	n/a
2	ATF1	chr7:112644827-112645228	K562	blood:	n/a	n/a
3	ATF1	chr7:112642741-112642792	K562	blood:	n/a	n/a
4	ATF1	chr7:112711587-112711816	K562	blood:	n/a	n/a
5	ATF3	chr7:112711542-112711857	K562	blood:	n/a	n/a
6	ATF3	chr7:112711624-112711766	K562	blood:	n/a	n/a
7	BACH1	chr7:112673397-112673415	K562	blood:	n/a	n/a
8	BACH1	chr7:112699090-112699105	K562	blood:	n/a	n/a
9	BATF	chr7:112644796-112645017	GM12878	blood:	n/a	n/a
10	CBX3	chr7:112652949-112653261	K562	blood:	n/a	n/a
11	CCNT2	chr7:112644880-112645469	K562	blood:	n/a	chr7:112644888-112644908
12	CEBPB	chr7:112688243-112688439	H1-hESC	embryonic stem cell:	n/a	chr7:112688334-112688351 chr7:112688337-112688348
13	CEBPB	chr7:112702740-112703014	H1-hESC	embryonic stem cell:	n/a	n/a
14	CEBPB	chr7:112688276-112688417	HepG2	liver:	n/a	chr7:112688334-112688351 chr7:112688337-112688348
15	CEBPB	chr7:112711559-112711855	K562	blood:	n/a	chr7:112711603-112711615 chr7:112711589-112711600
16	CEBPB	chr7:112702742-112703040	IMR90	lung:	n/a	n/a
17	CEBPB	chr7:112711542-112711893	K562	blood:	n/a	chr7:112711603-112711615 chr7:112711589-112711600
18	CEBPB	chr7:112637886-112638200	H1-hESC	embryonic stem cell:	n/a	n/a
19	CEBPB	chr7:112711621-112711841	IMR90	lung:	n/a	n/a
20	CEBPB	chr7:112702691-112703014	K562	blood:	n/a	n/a
21	CEBPB	chr7:112688266-112688501	K562	blood:	n/a	chr7:112688334-112688351 chr7:112688337-112688348
22	CEBPB	chr7:112667890-112668090	A549	lung:	n/a	chr7:112668019-112668030 chr7:112667917-112667928
23	CEBPB	chr7:112637901-112638269	HepG2	liver:	n/a	n/a
24	CEBPB	chr7:112702672-112702919	K562	blood:	n/a	n/a
25	CEBPB	chr7:112711532-112711901	K562	blood:	n/a	chr7:112711603-112711615 chr7:112711589-112711600
26	CEBPB	chr7:112711672-112711713	H1-hESC	embryonic stem cell:	n/a	n/a
27	CEBPB	chr7:112667913-112668127	HepG2	liver:	n/a	chr7:112668019-112668030 chr7:112667917-112667928
28	CEBPB	chr7:112667877-112668159	K562	blood:	n/a	chr7:112668019-112668030 chr7:112667917-112667928
29	CEBPB	chr7:112702779-112702967	HepG2	liver:	n/a	n/a
30	CEBPB	chr7:112712275-112712502	HepG2	liver:	n/a	chr7:112712381-112712392 chr7:112712382-112712393
31	CEBPB	chr7:112712264-112712565	IMR90	lung:	n/a	chr7:112712381-112712392 chr7:112712382-112712393
32	CEBPB	chr7:112632132-112632144	HepG2	liver:	n/a	n/a
33	CEBPD	chr7:112644923-112645626	K562	blood:	n/a	n/a
34	CEBPD	chr7:112644963-112645558	K562	blood:	n/a	n/a
35	CTCF	chr7:112655240-112655390	GM12865	blood:	n/a	chr7:112655259-112655277 chr7:112655260-112655276 chr7:112655261-112655282 chr7:112655262-112655271
36	CTCF	chr7:112654781-112655719	SK-N-SH	brain:	n/a	chr7:112655259-112655277 chr7:112655260-112655276 chr7:112655261-112655282 chr7:112655262-112655271
37	CTCF	chr7:112694479-112694571	GM13976	blood:	n/a	n/a
38	CTCF	chr7:112694548-112694601	ProgFib	skin:	n/a	n/a
39	CTCF	chr7:112655180-112655330	HCT-116	colon:	n/a	chr7:112655259-112655277 chr7:112655260-112655276 chr7:112655261-112655282 chr7:112655262-112655271
40	CTCF	chr7:112655180-112655330	GM12870	blood:	n/a	chr7:112655259-112655277 chr7:112655260-112655276 chr7:112655261-112655282 chr7:112655262-112655271
41	CTCF	chr7:112655180-112655330	HMEC	breast:	n/a	chr7:112655259-112655277 chr7:112655260-112655276 chr7:112655261-112655282 chr7:112655262-112655271
42	CTCF	chr7:112655060-112655210	BE2_C	brain:	n/a	n/a
43	CTCF	chr7:112655092-112655492	MCF-7	breast:	n/a	chr7:112655259-112655277 chr7:112655260-112655276 chr7:112655261-112655282 chr7:112655262-112655271
44	CTCF	chr7:112694484-112694594	MCF-7	breast:	n/a	n/a
45	CTCF	chr7:112655180-112655330	Caco-2	colon:	n/a	chr7:112655259-112655277 chr7:112655260-112655276 chr7:112655261-112655282 chr7:112655262-112655271
46	CTCF	chr7:112655160-112655310	HMF	breast:	n/a	chr7:112655259-112655277 chr7:112655260-112655276 chr7:112655261-112655282 chr7:112655262-112655271
47	CTCF	chr7:112655160-112655310	HRE	kidney:	n/a	chr7:112655259-112655277 chr7:112655260-112655276 chr7:112655261-112655282 chr7:112655262-112655271
48	CTCF	chr7:112694520-112694670	K562	blood:	n/a	n/a
49	CTCF	chr7:112644220-112644370	GM12865	blood:	n/a	n/a
50	CTCF	chr7:112655180-112655330	AoAF	blood vessel:	n/a	chr7:112655259-112655277 chr7:112655260-112655276 chr7:112655261-112655282 chr7:112655262-112655271

No.	Distal block	Cell Line	Cell type
1	chr7:112654683..112655746-chr7:113061433..113062375,3	K562	blood:
2	chr7:112628593..112630399-chr7:112648519..112650654,2	K562	blood:
3	chr7:112680260..112683174-chr7:112683232..112685538,2	MCF-7	breast:
4	chr7:112687592..112689937-chr7:112698080..112700516,2	K562	blood:
5	chr7:112509083..112509822-chr7:112654779..112655292,2	MCF-7	breast:
6	chr7:112654800..112655464-chr7:112754097..112754722,2	MCF-7	breast:
7	chr7:112629828..112632349-chr7:112641858..112644644,2	K562	blood:
8	chr7:112654983..112656027-chr7:113061405..113062486,9	MCF-7	breast:
9	chr7:112676603..112678329-chr7:112682041..112684598,2	K562	blood:
10	chr7:112703408..112705692-chr7:112716673..112719279,2	K562	blood:
11	chr7:112654853..112656193-chr7:112753393..112754620,7	MCF-7	breast:
12	chr7:112695979..112699168-chr7:112699243..112702331,3	K562	blood:
13	chr7:112696520..112698200-chr7:112699916..112702852,2	MCF-7	breast:
14	chr7:112676603..112678329-chr7:112682041..112684598,2	K562	blood:
15	chr7:112653832..112655497-chr7:112753115..112754776,2	MCF-7	breast:
16	chr7:112654663..112655993-chr7:113338417..113339149,3	MCF-7	breast:
17	chr7:112655287..112655802-chr7:113061468..113062197,2	MCF-7	breast:
18	chr7:112682248..112683838-chr7:112894672..112896979,2	K562	blood:
19	chr7:112713707..112715518-chr7:112717712..112719924,2	K562	blood:
20	chr7:112629828..112632349-chr7:112641858..112644644,2	K562	blood:
21	chr7:112655258..112655792-chr7:112749920..112750861,2	MCF-7	breast:
22	chr7:112687592..112689937-chr7:112698080..112700516,2	K562	blood:
23	chr7:112655256..112655797-chr7:112929374..112930128,2	MCF-7	breast:
24	chr7:112695979..112699168-chr7:112699243..112702331,3	K562	blood:
25	chr7:112680260..112683174-chr7:112683232..112685538,2	MCF-7	breast:
26	chr7:112696520..112698200-chr7:112699916..112702852,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C7orf60-1	chr7:112635623-112635698	NONHSAT122803
2	lnc-C7orf60-1	chr7:112635623-112635698	NONHSAT122806
3	lnc-C7orf60-1	chr7:112635623-112635698	NR_110162
4	lnc-C7orf60-1	chr7:112635623-112635712	NONHSAT122810
5	lnc-C7orf60-1	chr7:112635623-112635689	ENSG00000234520
6	lnc-C7orf60-1	chr7:112635623-112635698	NONHSAT122805
7	lnc-C7orf60-1	chr7:112635623-112635682	ENSG00000234520

Variant related genes	Relation type
ENSG00000234520	TF binding region

Extended variants
information (count: 1275 )
Associated
traits (count: 85 )

Variant overlapped rSNPs/rCNVs (count:1275 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs576871608	chr7:112631151-112631152	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs530006766	chr7:112631161-112631162	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs185246932	chr7:112631241-112631242	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs562363150	chr7:112631254-112631255	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs189714322	chr7:112631362-112631363	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs182066937	chr7:112631431-112631432	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs548111978	chr7:112631552-112631553	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs560006148	chr7:112631568-112631569	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs527529072	chr7:112631589-112631590	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs116599352	chr7:112631608-112631609	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs570586263	chr7:112631626-112631627	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs371447871	chr7:112631631-112631632	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs1569277	chr7:112631636-112631637	Weak transcription Enhancers Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs540712106	chr7:112631650-112631651	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs550219936	chr7:112631662-112631663	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs188034667	chr7:112631664-112631665	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs535836171	chr7:112631705-112631706	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs1569276	chr7:112631713-112631714	Weak transcription Enhancers Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
19	rs565492271	chr7:112631722-112631723	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs74832356	chr7:112631759-112631760	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs540094217	chr7:112631775-112631776	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs558396972	chr7:112631794-112631795	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs529956096	chr7:112631802-112631803	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs145750916	chr7:112631825-112631826	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs556206071	chr7:112631850-112631851	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs35598304	chr7:112631885-112631886	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs546564030	chr7:112631886-112631887	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs1562750	chr7:112631906-112631907	Weak transcription Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs1017598	chr7:112631910-112631911	Weak transcription Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs539058999	chr7:112632019-112632020	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs1017599	chr7:112632035-112632036	Weak transcription Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs552381776	chr7:112632048-112632049	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs527588744	chr7:112632063-112632064	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs1017600	chr7:112632068-112632069	Weak transcription Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs564149202	chr7:112632084-112632085	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs531512409	chr7:112632196-112632197	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs114226359	chr7:112632201-112632202	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs547519550	chr7:112632204-112632205	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs117061552	chr7:112632238-112632239	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs73416725	chr7:112632261-112632262	Weak transcription Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs566042430	chr7:112632323-112632324	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs540156633	chr7:112632348-112632349	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs112135971	chr7:112632376-112632377	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs191306881	chr7:112632406-112632407	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs570185701	chr7:112632427-112632428	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs537641107	chr7:112632436-112632437	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs556031482	chr7:112632441-112632442	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs148200752	chr7:112632500-112632501	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs541482316	chr7:112632642-112632643	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs553368452	chr7:112632676-112632677	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:85)

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
Acute myeloid leukemia	16864856	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
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21785460	CNVD
Chronic myeloid leukemia	21384125	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	21364760	CNVD
lymphocytic leukemia	21291569	CNVD
Basal cell lymphoma	17053054	CNVD
Prostate cancer	16573809	CNVD
Medulloblastoma	16783165	CNVD
Myelofibrosis	22110671	CNVD
Squamous cell cancer	20885788	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Breast cancer	16397240	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
Autism	19401682	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	19546859	CNVD
Schizophrenia	19546859	CNVD
Tourette syndrome	19546859	CNVD
Melanoma	19188590	CNVD
small cell lung cancer	20016488	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:162 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:112625000-112631200	Enhancers	Fetal Heart	heart
2	chr7:112626800-112631400	Enhancers	NH-A	brain
3	chr7:112627200-112631400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
4	chr7:112627400-112631600	Enhancers	Muscle Satellite Cultured Cells	--
5	chr7:112627800-112635200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
6	chr7:112628000-112635200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
7	chr7:112628600-112634800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
8	chr7:112628600-112635200	Weak transcription	NHLF	lung
9	chr7:112628800-112634800	Weak transcription	HSMMtube	muscle
10	chr7:112629600-112631200	Enhancers	HMEC	breast
11	chr7:112629800-112631200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
12	chr7:112629800-112631400	Enhancers	Osteobl	bone
13	chr7:112629800-112634200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
14	chr7:112630200-112631200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
15	chr7:112630400-112631200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
16	chr7:112630400-112631200	Enhancers	Placenta Amnion	Placenta Amnion
17	chr7:112630400-112631200	Enhancers	NHEK	skin
18	chr7:112630600-112634600	Weak transcription	HSMM	muscle
19	chr7:112630600-112635800	Active TSS	Right Ventricle	heart
20	chr7:112631000-112632000	Weak transcription	Left Ventricle	heart
21	chr7:112631000-112634800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
22	chr7:112631000-112634800	Weak transcription	NHDF-Ad	bronchial
23	chr7:112631200-112631600	Weak transcription	Fetal Heart	heart
24	chr7:112631200-112634400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
25	chr7:112631200-112634400	Weak transcription	HMEC	breast
26	chr7:112631200-112634800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
27	chr7:112631200-112634800	Weak transcription	NHEK	skin
28	chr7:112631200-112635200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
29	chr7:112631200-112635200	Weak transcription	Placenta Amnion	Placenta Amnion
30	chr7:112631400-112634200	Weak transcription	Osteobl	bone
31	chr7:112631400-112634400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
32	chr7:112631400-112634600	Weak transcription	NH-A	brain
33	chr7:112631600-112631800	Enhancers	Fetal Heart	heart
34	chr7:112631600-112634400	Weak transcription	Muscle Satellite Cultured Cells	--
35	chr7:112631800-112633800	Weak transcription	Fetal Heart	heart
36	chr7:112632000-112634000	Active TSS	Left Ventricle	heart
37	chr7:112632200-112635800	Active TSS	Right Atrium	heart
38	chr7:112633600-112634200	Enhancers	Fetal Brain Male	brain
39	chr7:112633800-112634800	Enhancers	Fetal Heart	heart
40	chr7:112634000-112634800	Weak transcription	Left Ventricle	heart
41	chr7:112634200-112634600	Enhancers	Osteobl	bone
42	chr7:112634200-112636000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
43	chr7:112634200-112637400	Weak transcription	Fetal Brain Male	brain
44	chr7:112634400-112634600	Enhancers	Muscle Satellite Cultured Cells	--
45	chr7:112634400-112634800	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
46	chr7:112634400-112634800	Active TSS	HMEC	breast
47	chr7:112634400-112635800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
48	chr7:112634600-112634800	Enhancers	HSMM	muscle
49	chr7:112634600-112634800	Flanking Active TSS	Osteobl	bone
50	chr7:112634600-112635200	Enhancers	NH-A	brain

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