Variant report

Variant	esv1819632
Chromosome Location	chr7:6749937-6767410
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	ATF2	chr7:6764660-6765106	GM12878	blood:	n/a	n/a
2	ATF2	chr7:6765435-6765872	GM12878	blood:	n/a	n/a
3	ATF2	chr7:6764577-6765116	GM12878	blood:	n/a	n/a
4	BATF	chr7:6764386-6765017	GM12878	blood:	n/a	n/a
5	BCL11A	chr7:6764490-6765004	GM12878	blood:	n/a	n/a
6	BCL3	chr7:6765434-6765865	GM12878	blood:	n/a	n/a
7	BCL3	chr7:6764602-6765093	GM12878	blood:	n/a	n/a
8	BCLAF1	chr7:6765486-6765849	GM12878	blood:	n/a	n/a
9	BCLAF1	chr7:6764543-6765036	GM12878	blood:	n/a	n/a
10	BHLHE40	chr7:6765444-6765862	GM12878	blood:	n/a	n/a
11	BHLHE40	chr7:6764639-6765044	GM12878	blood:	n/a	n/a
12	CHD1	chr7:6764785-6765290	GM12878	blood:	n/a	n/a
13	CTCF	chr7:6757880-6758030	Hela-S3	cervix:	n/a	chr7:6757947-6757965
14	CTCF	chr7:6757800-6757950	HPF	lung:	n/a	n/a
15	CTCF	chr7:6757900-6758050	GM06990	blood:	n/a	chr7:6757947-6757965
16	CTCF	chr7:6757900-6758050	HCFaa	heart:	n/a	chr7:6757947-6757965
17	CTCF	chr7:6757820-6757970	GM12866	blood:	n/a	chr7:6757947-6757965
18	CTCF	chr7:6757900-6758050	NB4	blood:	n/a	chr7:6757947-6757965
19	CTCF	chr7:6764660-6764810	GM06990	blood:	n/a	n/a
20	CTCF	chr7:6757900-6758050	HMEC	breast:	n/a	chr7:6757947-6757965
21	CTCF	chr7:6757920-6758070	HFF-Myc	foreskin:	n/a	chr7:6757947-6757965
22	CTCF	chr7:6757830-6758069	K562	blood:	n/a	chr7:6757947-6757965
23	CTCF	chr7:6756448-6756470	Kidney_OC	kidney:	n/a	n/a
24	CTCF	chr7:6757929-6757980	Pancreas_OC	pancreas:	n/a	chr7:6757947-6757965
25	CTCF	chr7:6757780-6758050	NHEK	skin:	n/a	chr7:6757947-6757965
26	CTCF	chr7:6757820-6757970	HA-sp	spinal cord:	n/a	chr7:6757947-6757965
27	CTCF	chr7:6757840-6757990	GM12873	blood:	n/a	chr7:6757947-6757965
28	CTCF	chr7:6757875-6758035	GM10266	blood:	n/a	chr7:6757947-6757965
29	CTCF	chr7:6757860-6758010	Caco-2	colon:	n/a	chr7:6757947-6757965
30	CTCF	chr7:6757880-6758030	GM12874	blood:	n/a	chr7:6757947-6757965
31	CTCF	chr7:6757880-6758030	GM12864	blood:	n/a	chr7:6757947-6757965
32	CTCF	chr7:6757920-6758070	GM12878	blood:	n/a	chr7:6757947-6757965
33	CTCF	chr7:6757897-6758012	H1-hESC	embryonic stem cell:	n/a	chr7:6757947-6757965
34	CTCF	chr7:6757860-6758010	HUVEC	blood vessel:	n/a	chr7:6757947-6757965
35	CTCF	chr7:6764666-6764687	GM12891	blood:	n/a	n/a
36	CTCF	chr7:6757847-6758013	HepG2	liver:	n/a	chr7:6757947-6757965
37	CTCF	chr7:6757900-6758050	HMF	breast:	n/a	chr7:6757947-6757965
38	CTCF	chr7:6757900-6758050	GM12867	blood:	n/a	chr7:6757947-6757965
39	CTCF	chr7:6757880-6758030	HCM	heart:	n/a	chr7:6757947-6757965
40	CTCF	chr7:6757880-6758030	HCPEpiC	choroid plexus:	n/a	chr7:6757947-6757965
41	CTCF	chr7:6757880-6758030	K562	blood:	n/a	chr7:6757947-6757965
42	CTCF	chr7:6764672-6764675	GM19238	blood:	n/a	n/a
43	CTCF	chr7:6757796-6758103	K562	blood:	n/a	chr7:6757947-6757965
44	CTCF	chr7:6757820-6757970	AG09319	gingival:	n/a	chr7:6757947-6757965
45	CTCF	chr7:6757900-6758050	GM12873	blood:	n/a	chr7:6757947-6757965
46	CTCF	chr7:6757792-6758000	K562	blood:	n/a	chr7:6757947-6757965
47	CTCF	chr7:6764714-6764764	GM10266	blood:	n/a	n/a
48	CTCF	chr7:6757880-6758030	GM12865	blood:	n/a	chr7:6757947-6757965
49	CTCF	chr7:6757926-6757981	HepG2	liver:	n/a	chr7:6757947-6757965
50	CTCF	chr7:6764739-6764762	GM19240	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:6750462-6750512	HCT-116	colon:	n/a
2	chr7:6766092-6766142	HCM	heart:	n/a
3	chr7:6750462-6750512	BE2_C	brain:	n/a
4	chr7:6766092-6766142	A549	lung:	n/a
5	chr7:6766092-6766142	AG09319	gingival:	n/a
6	chr7:6750462-6750512	A549	lung:	n/a
7	chr7:6750462-6750512	SK-N-SH	brain:	n/a
8	chr7:6750462-6750512	MCF-7	breast:	n/a
9	chr7:6766092-6766142	ProgFib	skin:	n/a
10	chr7:6766092-6766142	RPTEC	kidney:	n/a
11	chr7:6750462-6750512	GM12878	blood:	n/a
12	chr7:6766092-6766142	HCT-116	colon:	n/a
13	chr7:6750462-6750512	NB4	blood:	n/a
14	chr7:6750462-6750512	SK-N-MC	brain:	n/a
15	chr7:6750462-6750512	HEEpiC	esophagus:	n/a
16	chr7:6750462-6750512	HRE	kidney:	n/a
17	chr7:6750462-6750512	Hepatocyte	liver:	n/a
18	chr7:6766092-6766142	NT2-D1	testis:	n/a
19	chr7:6750462-6750512	MCF10A-Er-Src	breast:	n/a
20	chr7:6750462-6750512	SK-N-SH_RA	brain:	n/a
21	chr7:6750462-6750512	HAEpiC	amniotic membrane:	n/a
22	chr7:6766092-6766142	GM12878	blood:	n/a
23	chr7:6766092-6766142	U87	brain:	n/a
24	chr7:6750462-6750512	AG04450	lung:	fetal
25	chr7:6766092-6766142	AG10803	skin:	n/a
26	chr7:6766092-6766142	HRE	kidney:	n/a
27	chr7:6750462-6750512	HRPEpiC	eye:	n/a
28	chr7:6750462-6750512	AG04449	skin:	fetal
29	chr7:6750462-6750512	NT2-D1	testis:	n/a
30	chr7:6750462-6750512	U87	brain:	n/a
31	chr7:6750462-6750512	LNCaP	prostate:	n/a
32	chr7:6750462-6750512	H1-hESC	embryonic stem cell:	embryo
33	chr7:6750462-6750512	AG09319	gingival:	n/a
34	chr7:6750462-6750512	HCPEpiC	choroid plexus:	n/a
35	chr7:6750462-6750512	GM06990	blood:	n/a
36	chr7:6766092-6766142	AG04450	lung:	fetal
37	chr7:6766092-6766142	MCF10A-Er-Src	breast:	n/a
38	chr7:6750462-6750512	AoSMC	blood vessel:	n/a
39	chr7:6750462-6750512	AG10803	skin:	n/a
40	chr7:6766092-6766142	CMK	blood:	n/a
41	chr7:6750462-6750512	GM12891	blood:	n/a
42	chr7:6766092-6766142	Jurkat	blood:	n/a
43	chr7:6750462-6750512	Caco-2	colon:	n/a
44	chr7:6766092-6766142	HEK293	kidney:	embryo
45	chr7:6750462-6750512	CMK	blood:	n/a
46	chr7:6766092-6766142	Hela-S3	cervix:	n/a
47	chr7:6766092-6766142	AoSMC	blood vessel:	n/a
48	chr7:6750462-6750512	NH-A	brain:	n/a
49	chr7:6766092-6766142	NHDF-neo	bronchial:	n/a
50	chr7:6766092-6766142	BJ	skin:	n/a

No.	Distal block	Cell Line	Cell type
1	chr7:6761698..6764136-chr7:6769053..6770920,2	MCF-7	breast:
2	chr7:6755281..6757989-chr7:6768169..6769805,2	K562	blood:
3	chr7:6616941..6618678-chr7:6767339..6769412,2	MCF-7	breast:
4	chr7:6745105..6747702-chr7:6760857..6762901,2	MCF-7	breast:
5	chr7:6745040..6747820-chr7:6753016..6755979,2	K562	blood:
6	chr7:6766860..6769459-chr7:6864426..6866111,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AC073343.1-1	chr7:6750381-6750402	NONHSAT119061
2	lnc-AC073343.1-1	chr7:6751010-6751093	NONHSAT119062
3	lnc-AC073343.1-1	chr7:6751010-6751133	NONHSAT119061

Variant related genes	Relation type
ZNF12	TF binding region
PMS2CL	TF binding region
ZNF12	CpG island
PMS2CL	CpG island
ENSG00000146574	chromatin interactions
ENSG00000136247	chromatin interactions
ENSG00000164631	chromatin interactions
ENSG00000187953	chromatin interactions

Extended variants
information (count: 894 )
Associated
traits (count: 77 )

Variant overlapped rSNPs/rCNVs (count:894 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs541327991	chr7:6749941-6749942	ZNF genes & repeats Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs530355696	chr7:6749946-6749947	ZNF genes & repeats Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs560016868	chr7:6749988-6749989	ZNF genes & repeats Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs533483201	chr7:6750004-6750005	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs139463322	chr7:6750010-6750011	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs144976412	chr7:6750011-6750012	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs139267889	chr7:6750051-6750052	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs375140212	chr7:6750054-6750055	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs531025953	chr7:6750063-6750064	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs183000736	chr7:6750066-6750067	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs548450289	chr7:6750067-6750068	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs528505222	chr7:6750094-6750095	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs547346897	chr7:6750107-6750108	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs6969066	chr7:6750112-6750113	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs187603751	chr7:6750131-6750132	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs557925158	chr7:6750156-6750157	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs569516654	chr7:6750187-6750188	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs112313126	chr7:6750265-6750266	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs147138566	chr7:6750273-6750274	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs192586779	chr7:6750279-6750280	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs573274281	chr7:6750317-6750318	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs140443169	chr7:6750319-6750320	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs552725290	chr7:6750334-6750335	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs538570033	chr7:6750343-6750344	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs556519619	chr7:6750367-6750368	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs112776876	chr7:6750377-6750378	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs184119581	chr7:6750393-6750394	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
28	rs541700631	chr7:6750395-6750396	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
29	rs550603266	chr7:6750447-6750448	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs568978817	chr7:6750448-6750449	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs187906123	chr7:6750452-6750453	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs543113032	chr7:6750462-6750463	Weak transcription Enhancers	CpG island	1 gene(s)	Overlapped CNVs	n/a
33	rs374074862	chr7:6750469-6750470	Weak transcription Enhancers	CpG island	1 gene(s)	Overlapped CNVs	n/a
34	rs77714679	chr7:6750494-6750495	Weak transcription Enhancers	CpG island	1 gene(s)	Overlapped CNVs	n/a
35	rs370268577	chr7:6750534-6750535	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs546957203	chr7:6750535-6750536	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs60514449	chr7:6750543-6750544	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs533254097	chr7:6750554-6750555	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs554194307	chr7:6750564-6750565	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs368845283	chr7:6750580-6750581	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs149688386	chr7:6750589-6750590	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs192491132	chr7:6750603-6750604	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs536867889	chr7:6750614-6750615	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs548792719	chr7:6750624-6750625	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs567336186	chr7:6750630-6750631	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs534458354	chr7:6750632-6750633	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs112806901	chr7:6750658-6750659	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs552928601	chr7:6750700-6750701	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs145367027	chr7:6750734-6750735	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs184873585	chr7:6750748-6750749	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:77)

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
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
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
Acute myeloid leukemia	21251322	CNVD
Glioblastoma multiforme	21525872	CNVD
Autism	20685689	CNVD
Breast cancer	22522925	CNVD
Ovarian cancer	21781307	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:53 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:6747000-6768600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr7:6747400-6750600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
3	chr7:6747400-6752600	Weak transcription	HSMMtube	muscle
4	chr7:6747400-6757400	Weak transcription	Fetal Brain Female	brain
5	chr7:6749600-6750000	ZNF genes & repeats	H9 Cell Line	embryonic stem cell
6	chr7:6749800-6750000	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr7:6749800-6750000	Flanking Active TSS	Liver	Liver
8	chr7:6750000-6750400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr7:6750000-6750600	Enhancers	Liver	Liver
10	chr7:6750600-6752200	Weak transcription	Liver	Liver
11	chr7:6752200-6754600	Strong transcription	Liver	Liver
12	chr7:6754600-6768600	Weak transcription	Liver	Liver
13	chr7:6759400-6759600	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
14	chr7:6763600-6766600	Enhancers	Primary B cells from cord blood	blood
15	chr7:6764000-6765800	Enhancers	Primary hematopoietic stem cells short term culture	blood
16	chr7:6764000-6766200	Enhancers	Primary B cells from peripheral blood	blood
17	chr7:6764200-6764600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
18	chr7:6764200-6765800	Enhancers	Primary hematopoietic stem cells	blood
19	chr7:6764200-6766200	Enhancers	GM12878-XiMat	blood
20	chr7:6764400-6765200	Enhancers	Primary neutrophils fromperipheralblood	blood
21	chr7:6764400-6765400	Enhancers	Primary monocytes fromperipheralblood	blood
22	chr7:6764400-6765800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
23	chr7:6764600-6764800	Enhancers	ES-I3 Cell Line	embryonic stem cell
24	chr7:6764600-6764800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
25	chr7:6764600-6764800	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
26	chr7:6764600-6765200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
27	chr7:6764600-6765200	Enhancers	Spleen	Spleen
28	chr7:6764600-6765800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
29	chr7:6764800-6765000	Enhancers	Monocytes-CD14+_RO01746	blood
30	chr7:6765000-6765200	Enhancers	Sigmoid Colon	Sigmoid Colon
31	chr7:6765000-6768600	Weak transcription	Monocytes-CD14+_RO01746	blood
32	chr7:6765200-6765800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
33	chr7:6765200-6766000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
34	chr7:6765200-6768600	Weak transcription	Primary neutrophils fromperipheralblood	blood
35	chr7:6765200-6769000	Weak transcription	Spleen	Spleen
36	chr7:6765400-6768600	Weak transcription	Sigmoid Colon	Sigmoid Colon
37	chr7:6765800-6768400	Weak transcription	Primary hematopoietic stem cells	blood
38	chr7:6765800-6768400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
39	chr7:6765800-6768600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
40	chr7:6765800-6768600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
41	chr7:6765800-6768600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
42	chr7:6766000-6766400	Enhancers	NHEK	skin
43	chr7:6766200-6766400	Enhancers	ES-I3 Cell Line	embryonic stem cell
44	chr7:6766200-6766400	Enhancers	Placenta	Placenta
45	chr7:6766200-6768400	Weak transcription	GM12878-XiMat	blood
46	chr7:6766200-6768800	Weak transcription	Primary B cells from peripheral blood	blood
47	chr7:6766200-6769000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
48	chr7:6766400-6768600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
49	chr7:6766400-6769000	Weak transcription	NHEK	skin
50	chr7:6766600-6768600	Weak transcription	Primary B cells from cord blood	blood

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links