Variant report

Variant	nsv1019962
Chromosome Location	chr7:12683139-12699056
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:362)
CpG islands
(count:0)
Chromatin interactive
region (count:15)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:362 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:12687061-12687778	K562	blood:	n/a	n/a
2	ARID3A	chr7:12687054-12687777	HepG2	liver:	n/a	n/a
3	ATF1	chr7:12683358-12683669	K562	blood:	n/a	n/a
4	ATF1	chr7:12687293-12687728	K562	blood:	n/a	n/a
5	ATF3	chr7:12687338-12687753	A549	lung:	n/a	n/a
6	ATF3	chr7:12687336-12687782	K562	blood:	n/a	n/a
7	ATF3	chr7:12687438-12687677	K562	blood:	n/a	n/a
8	BACH1	chr7:12687352-12687760	K562	blood:	n/a	n/a
9	BACH1	chr7:12687423-12687657	H1-hESC	embryonic stem cell:	n/a	n/a
10	BCL3	chr7:12687250-12687685	A549	lung:	n/a	n/a
11	BCL3	chr7:12687152-12687769	A549	lung:	n/a	n/a
12	BHLHE40	chr7:12687416-12687697	A549	lung:	n/a	n/a
13	BHLHE40	chr7:12687372-12687752	HepG2	liver:	n/a	n/a
14	BHLHE40	chr7:12686990-12687821	K562	blood:	n/a	n/a
15	BRCA1	chr7:12687006-12687739	Hela-S3	cervix:	n/a	n/a
16	BRCA1	chr7:12692766-12693706	Hela-S3	cervix:	n/a	n/a
17	CBX3	chr7:12686923-12687798	K562	blood:	n/a	n/a
18	CBX3	chr7:12687038-12687889	HCT-116	colon:	n/a	n/a
19	CBX3	chr7:12687310-12687747	K562	blood:	n/a	n/a
20	CCNT2	chr7:12688708-12688875	K562	blood:	n/a	n/a
21	CCNT2	chr7:12687269-12687708	K562	blood:	n/a	n/a
22	CEBPB	chr7:12687265-12687745	A549	lung:	n/a	n/a
23	CEBPB	chr7:12692671-12692763	H1-hESC	embryonic stem cell:	n/a	n/a
24	CEBPB	chr7:12687309-12687798	MCF-7	breast:	n/a	n/a
25	CEBPB	chr7:12692559-12692800	K562	blood:	n/a	n/a
26	CEBPB	chr7:12687258-12687694	K562	blood:	n/a	n/a
27	CEBPB	chr7:12692243-12693738	Hela-S3	cervix:	n/a	n/a
28	CEBPB	chr7:12692664-12692858	A549	lung:	n/a	n/a
29	CEBPB	chr7:12692578-12692932	MCF-7	breast:	n/a	n/a
30	CEBPB	chr7:12687005-12687783	Hela-S3	cervix:	n/a	n/a
31	CEBPB	chr7:12687371-12687672	MCF-7	breast:	n/a	n/a
32	CEBPD	chr7:12687203-12687609	K562	blood:	n/a	n/a
33	CEBPD	chr7:12687008-12687789	K562	blood:	n/a	n/a
34	CHD2	chr7:12687117-12687807	Hela-S3	cervix:	n/a	n/a
35	CTCF	chr7:12696480-12696526	Fibrobl	skin:	n/a	n/a
36	E2F4	chr7:12692927-12693135	MCF10A-Er-Src	breast:	n/a	n/a
37	E2F6	chr7:12687471-12687640	K562	blood:	n/a	n/a
38	E2F6	chr7:12685818-12686295	H1-hESC	embryonic stem cell:	n/a	n/a
39	E2F6	chr7:12685901-12686207	H1-hESC	embryonic stem cell:	n/a	n/a
40	EBF1	chr7:12684920-12685177	GM12878	blood:	n/a	n/a
41	EBF1	chr7:12683315-12683686	GM12878	blood:	n/a	n/a
42	ELF1	chr7:12687157-12687797	MCF-7	breast:	n/a	n/a
43	EP300	chr7:12687314-12687699	SK-N-SH_RA	brain:	n/a	chr7:12687372-12687382
44	EP300	chr7:12693192-12693477	SK-N-SH_RA	brain:	n/a	n/a
45	EP300	chr7:12692581-12693721	SK-N-SH	brain:	n/a	n/a
46	EP300	chr7:12686991-12687864	SK-N-SH	brain:	n/a	chr7:12687372-12687382
47	EP300	chr7:12687234-12687782	ECC-1	luminal epithelium:	n/a	chr7:12687372-12687382
48	EP300	chr7:12687292-12687716	HepG2	liver:	n/a	chr7:12687372-12687382
49	EP300	chr7:12687262-12687677	T-47D	breast:	n/a	chr7:12687372-12687382
50	EP300	chr7:12687079-12687843	A549	lung:	n/a	chr7:12687372-12687382

No data

(count:15 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:12687556..12689303-chr7:12690937..12696267,4	K562	blood:
2	chr7:12676312..12680625-chr7:12682268..12685378,4	K562	blood:
3	chr7:12678425..12679033-chr7:12691913..12692722,2	MCF-7	breast:
4	chr7:12684851..12686934-chr7:12726641..12728591,2	MCF-7	breast:
5	chr7:12678093..12680309-chr7:12682358..12684176,2	MCF-7	breast:
6	chr7:12688601..12690715-chr7:12695184..12696876,2	MCF-7	breast:
7	chr7:12693867..12695547-chr7:12707660..12709430,2	K562	blood:
8	chr7:12686745..12688830-chr7:12726079..12727852,2	MCF-7	breast:
9	chr7:12684743..12688656-chr7:12726864..12728584,4	K562	blood:
10	chr7:12687097..12689372-chr7:13046142..13048475,2	K562	blood:
11	chr7:12681447..12684050-chr7:12723257..12726126,2	K562	blood:
12	chr7:12683953..12687646-chr7:12726784..12729753,4	K562	blood:
13	chr7:12688601..12690715-chr7:12695184..12696876,2	MCF-7	breast:
14	chr7:12690884..12693877-chr7:12694168..12697345,4	K562	blood:
15	chr7:12688194..12690298-chr7:12711054..12712934,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SCIN-1	chr7:12694486-12694610	ENSG00000229233
2	lnc-SCIN-1	chr7:12693804-12694110	ENSG00000229233

No data

Variant related genes	Relation type
ENSG00000229233	TF binding region
ENSG00000271253	chromatin interactions
ENSG00000122644	chromatin interactions
ENSG00000229233	chromatin interactions

Extended variants
information (count: 774 )
Associated
traits (count: 84 )

Variant overlapped rSNPs/rCNVs (count:774 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2691812	chr7:12683139-12683140	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs62448334	chr7:12683146-12683147	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs182471902	chr7:12683169-12683170	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs555345581	chr7:12683184-12683185	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs553169247	chr7:12683192-12683193	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs557494907	chr7:12683197-12683198	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs540962816	chr7:12683198-12683199	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs560094665	chr7:12683200-12683201	Enhancers Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs576871904	chr7:12683236-12683237	Enhancers Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs368205189	chr7:12683247-12683248	Enhancers Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs545970396	chr7:12683253-12683254	Enhancers Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs563009285	chr7:12683255-12683256	Enhancers Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs116672119	chr7:12683378-12683379	Enhancers Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs548783239	chr7:12683382-12683383	Enhancers Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs562331537	chr7:12683401-12683402	Enhancers Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs375042231	chr7:12683416-12683417	Enhancers Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs12113631	chr7:12683446-12683447	Enhancers Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs548135466	chr7:12683475-12683476	Enhancers Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs570454762	chr7:12683500-12683501	Enhancers Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs570918273	chr7:12683507-12683508	Enhancers Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs574558922	chr7:12683582-12683583	Enhancers Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs539931205	chr7:12683590-12683591	Enhancers Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs2691811	chr7:12683604-12683605	Enhancers Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs111417819	chr7:12683609-12683610	Enhancers Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs535261727	chr7:12683616-12683617	Enhancers Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs150128833	chr7:12683631-12683632	Enhancers Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs565568245	chr7:12683637-12683638	Enhancers Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs34346327	chr7:12683656-12683657	Enhancers Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs369631686	chr7:12683703-12683704	Enhancers Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs373456652	chr7:12683712-12683713	Enhancers Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs577121947	chr7:12683718-12683719	Enhancers Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs149261452	chr7:12683772-12683773	Enhancers Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs146188527	chr7:12683776-12683777	Enhancers Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs371472039	chr7:12683795-12683796	Enhancers Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs377239353	chr7:12683798-12683799	Enhancers Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs186991856	chr7:12683807-12683808	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs374061565	chr7:12683813-12683814	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs190535249	chr7:12683818-12683819	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs372438836	chr7:12683819-12683820	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs1061889	chr7:12683895-12683896	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs376426782	chr7:12683896-12683897	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs1061890	chr7:12683900-12683901	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs201777088	chr7:12683903-12683904	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs1138957	chr7:12683915-12683916	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs369378047	chr7:12683930-12683931	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs373351911	chr7:12683931-12683932	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs200421074	chr7:12683943-12683944	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs369290622	chr7:12683955-12683956	Enhancers Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs532767293	chr7:12683971-12683972	Enhancers Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs199783300	chr7:12683987-12683988	Enhancers Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:84)

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
Cancer	21637783	CNVD
Squamous cell cancer	20885788	CNVD
Breast cancer	16397240	CNVD
Glioblastoma multiforme	17002787	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:190 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:12663800-12693000	Weak transcription	Pancreatic Islets	Pancreatic Islet
2	chr7:12664800-12700200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr7:12675800-12686000	Weak transcription	Adipose Nuclei	Adipose
4	chr7:12675800-12699800	Weak transcription	Esophagus	oesophagus
5	chr7:12678000-12687000	Weak transcription	Muscle Satellite Cultured Cells	--
6	chr7:12678200-12683200	Weak transcription	K562	blood
7	chr7:12678200-12687000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
8	chr7:12678400-12683200	Weak transcription	Lung	lung
9	chr7:12678600-12685800	Weak transcription	Stomach Mucosa	stomach
10	chr7:12679000-12685800	Weak transcription	Hela-S3	cervix
11	chr7:12679000-12688600	Weak transcription	Fetal Kidney	kidney
12	chr7:12679000-12693800	Weak transcription	Colonic Mucosa	Colon
13	chr7:12679400-12686200	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
14	chr7:12679800-12685400	Weak transcription	A549	lung
15	chr7:12680200-12683600	Enhancers	HepG2	liver
16	chr7:12680400-12683600	Strong transcription	Rectal Mucosa Donor 29	rectum
17	chr7:12681000-12683200	Weak transcription	Duodenum Mucosa	Duodenum
18	chr7:12681000-12685800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
19	chr7:12681000-12685800	Weak transcription	Placenta	Placenta
20	chr7:12681000-12687000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
21	chr7:12681000-12688400	Weak transcription	Fetal Stomach	stomach
22	chr7:12681400-12690800	Weak transcription	Rectal Mucosa Donor 31	rectum
23	chr7:12682000-12684200	Strong transcription	Brain Anterior Caudate	brain
24	chr7:12682200-12683400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
25	chr7:12682400-12683200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
26	chr7:12682400-12683200	Enhancers	Osteobl	bone
27	chr7:12682400-12683400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
28	chr7:12682400-12693400	Weak transcription	Sigmoid Colon	Sigmoid Colon
29	chr7:12682600-12683600	Enhancers	NH-A	brain
30	chr7:12682800-12683200	Weak transcription	Placenta Amnion	Placenta Amnion
31	chr7:12682800-12684000	Enhancers	Primary B cells from peripheral blood	blood
32	chr7:12682800-12687000	Weak transcription	NHDF-Ad	bronchial
33	chr7:12683000-12683400	Enhancers	Primary B cells from cord blood	blood
34	chr7:12683000-12683400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
35	chr7:12683000-12683800	Enhancers	Primary monocytes fromperipheralblood	blood
36	chr7:12683000-12683800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
37	chr7:12683000-12684000	Enhancers	Monocytes-CD14+_RO01746	blood
38	chr7:12683000-12686800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
39	chr7:12683200-12683400	Enhancers	Lung	lung
40	chr7:12683200-12683400	Enhancers	Placenta Amnion	Placenta Amnion
41	chr7:12683200-12683600	Strong transcription	Duodenum Mucosa	Duodenum
42	chr7:12683200-12683800	Genic enhancers	K562	blood
43	chr7:12683200-12684000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
44	chr7:12683200-12685200	Weak transcription	Osteobl	bone
45	chr7:12683200-12685400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
46	chr7:12683400-12683600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
47	chr7:12683400-12687000	Weak transcription	Placenta Amnion	Placenta Amnion
48	chr7:12683400-12687400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
49	chr7:12683600-12685000	Weak transcription	HepG2	liver
50	chr7:12683600-12685400	Weak transcription	NH-A	brain

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links