Variant report

Variant	esv10861
Chromosome Location	chr7:6749172-6768435
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:277)
CpG islands
(count:183)
Chromatin interactive
region (count:12)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:277 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:6749446-6749789	HepG2	liver:	n/a	n/a
2	ATF2	chr7:6764660-6765106	GM12878	blood:	n/a	n/a
3	ATF2	chr7:6764577-6765116	GM12878	blood:	n/a	n/a
4	ATF2	chr7:6765435-6765872	GM12878	blood:	n/a	n/a
5	BATF	chr7:6764386-6765017	GM12878	blood:	n/a	n/a
6	BCL11A	chr7:6764490-6765004	GM12878	blood:	n/a	n/a
7	BCL3	chr7:6764602-6765093	GM12878	blood:	n/a	n/a
8	BCL3	chr7:6765434-6765865	GM12878	blood:	n/a	n/a
9	BCLAF1	chr7:6765486-6765849	GM12878	blood:	n/a	n/a
10	BCLAF1	chr7:6764543-6765036	GM12878	blood:	n/a	n/a
11	BHLHE40	chr7:6765444-6765862	GM12878	blood:	n/a	n/a
12	BHLHE40	chr7:6764639-6765044	GM12878	blood:	n/a	n/a
13	CBX3	chr7:6749453-6749879	K562	blood:	n/a	n/a
14	CBX3	chr7:6749398-6749899	HCT-116	colon:	n/a	n/a
15	CBX3	chr7:6749454-6749792	K562	blood:	n/a	n/a
16	CHD1	chr7:6764785-6765290	GM12878	blood:	n/a	n/a
17	CHD2	chr7:6749610-6749810	HepG2	liver:	n/a	n/a
18	CTCF	chr7:6757900-6758050	HMEC	breast:	n/a	chr7:6757947-6757965
19	CTCF	chr7:6757880-6758030	K562	blood:	n/a	chr7:6757947-6757965
20	CTCF	chr7:6764701-6764709	GM10266	blood:	n/a	n/a
21	CTCF	chr7:6757920-6758070	GM12872	blood:	n/a	chr7:6757947-6757965
22	CTCF	chr7:6757840-6757990	MCF-7	breast:	n/a	chr7:6757947-6757965
23	CTCF	chr7:6757853-6758032	GM10248	blood:	n/a	chr7:6757947-6757965
24	CTCF	chr7:6764729-6764734	GM12891	blood:	n/a	n/a
25	CTCF	chr7:6764651-6764777	GM12892	blood:	n/a	n/a
26	CTCF	chr7:6757914-6758033	GM12892	blood:	n/a	chr7:6757947-6757965
27	CTCF	chr7:6757853-6758049	GM12878	blood:	n/a	chr7:6757947-6757965
28	CTCF	chr7:6757875-6758035	GM10266	blood:	n/a	chr7:6757947-6757965
29	CTCF	chr7:6757900-6758050	HMF	breast:	n/a	chr7:6757947-6757965
30	CTCF	chr7:6764660-6764810	GM06990	blood:	n/a	n/a
31	CTCF	chr7:6757829-6758104	K562	blood:	n/a	chr7:6757947-6757965
32	CTCF	chr7:6758160-6758310	GM12873	blood:	n/a	n/a
33	CTCF	chr7:6764729-6764796	Spleen_OC	spleen:	n/a	n/a
34	CTCF	chr7:6755722-6755792	K562	blood:	n/a	n/a
35	CTCF	chr7:6757880-6758030	GM12865	blood:	n/a	chr7:6757947-6757965
36	CTCF	chr7:6757880-6758030	AG09309	skin:	n/a	chr7:6757947-6757965
37	CTCF	chr7:6757841-6758103	GM12878	blood:	n/a	chr7:6757947-6757965
38	CTCF	chr7:6757880-6758030	HCM	heart:	n/a	chr7:6757947-6757965
39	CTCF	chr7:6757792-6758000	K562	blood:	n/a	chr7:6757947-6757965
40	CTCF	chr7:6757860-6758010	GM12865	blood:	n/a	chr7:6757947-6757965
41	CTCF	chr7:6757897-6758012	H1-hESC	embryonic stem cell:	n/a	chr7:6757947-6757965
42	CTCF	chr7:6757880-6758030	Hela-S3	cervix:	n/a	chr7:6757947-6757965
43	CTCF	chr7:6757920-6758070	SAEC	small airway:	n/a	chr7:6757947-6757965
44	CTCF	chr7:6757860-6758010	GM12872	blood:	n/a	chr7:6757947-6757965
45	CTCF	chr7:6757796-6758103	K562	blood:	n/a	chr7:6757947-6757965
46	CTCF	chr7:6757889-6758040	GM19238	blood:	n/a	chr7:6757947-6757965
47	CTCF	chr7:6757940-6758090	RPTEC	kidney:	n/a	chr7:6757947-6757965
48	CTCF	chr7:6757900-6758050	HCFaa	heart:	n/a	chr7:6757947-6757965
49	CTCF	chr7:6757860-6758010	HUVEC	blood vessel:	n/a	chr7:6757947-6757965
50	CTCF	chr7:6757840-6757990	GM12873	blood:	n/a	chr7:6757947-6757965

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:6749638-6749688	HUVEC	blood vessel:	n/a
2	chr7:6749638-6749688	HIPEpiC	eye:	n/a
3	chr7:6766092-6766142	HCPEpiC	choroid plexus:	n/a
4	chr7:6750462-6750512	HRPEpiC	eye:	n/a
5	chr7:6749638-6749688	T-47D	breast:	n/a
6	chr7:6766092-6766142	GM19239	blood:	n/a
7	chr7:6749638-6749688	NH-A	brain:	n/a
8	chr7:6749638-6749688	HNPCEpiC	eye:	n/a
9	chr7:6750462-6750512	SAEC	small airway:	n/a
10	chr7:6750462-6750512	GM12878	blood:	n/a
11	chr7:6766092-6766142	AG10803	skin:	n/a
12	chr7:6766092-6766142	NT2-D1	testis:	n/a
13	chr7:6766092-6766142	SK-N-MC	brain:	n/a
14	chr7:6766092-6766142	AG04449	skin:	fetal
15	chr7:6766092-6766142	HRE	kidney:	n/a
16	chr7:6766092-6766142	NB4	blood:	n/a
17	chr7:6749638-6749688	AoSMC	blood vessel:	n/a
18	chr7:6749638-6749688	Hela-S3	cervix:	n/a
19	chr7:6749638-6749688	GM19239	blood:	n/a
20	chr7:6749638-6749688	HCPEpiC	choroid plexus:	n/a
21	chr7:6749638-6749688	ProgFib	skin:	n/a
22	chr7:6766092-6766142	PFSK-1	brain:	n/a
23	chr7:6749638-6749688	HRCEpiC	kidney:	n/a
24	chr7:6749638-6749688	AG10803	skin:	n/a
25	chr7:6749638-6749688	HCF	heart:	n/a
26	chr7:6749638-6749688	A549	lung:	n/a
27	chr7:6750462-6750512	HRCEpiC	kidney:	n/a
28	chr7:6749638-6749688	GM06990	blood:	n/a
29	chr7:6749638-6749688	RPTEC	kidney:	n/a
30	chr7:6750462-6750512	NB4	blood:	n/a
31	chr7:6749638-6749688	IMR90	lung:	fetal
32	chr7:6749638-6749688	GM12891	blood:	n/a
33	chr7:6766092-6766142	MCF10A-Er-Src	breast:	n/a
34	chr7:6766092-6766142	U87	brain:	n/a
35	chr7:6766092-6766142	HEK293	kidney:	embryo
36	chr7:6750462-6750512	NHDF-neo	bronchial:	n/a
37	chr7:6750462-6750512	T-47D	breast:	n/a
38	chr7:6766092-6766142	BE2_C	brain:	n/a
39	chr7:6766092-6766142	LNCaP	prostate:	n/a
40	chr7:6750462-6750512	AoSMC	blood vessel:	n/a
41	chr7:6749638-6749688	K562	blood:	n/a
42	chr7:6766092-6766142	BJ	skin:	n/a
43	chr7:6766092-6766142	Hepatocyte	liver:	n/a
44	chr7:6766092-6766142	PANC-1	pancreas:	n/a
45	chr7:6749638-6749688	SK-N-SH_RA	brain:	n/a
46	chr7:6750462-6750512	NHBE	bronchial:	n/a
47	chr7:6750462-6750512	HCT-116	colon:	n/a
48	chr7:6750462-6750512	MCF-7	breast:	n/a
49	chr7:6750462-6750512	SK-N-MC	brain:	n/a
50	chr7:6749638-6749688	NB4	blood:	n/a

(count:12 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:6744871..6747873-chr7:6767656..6771321,4	K562	blood:
2	chr7:6745040..6747820-chr7:6753016..6755979,2	K562	blood:
3	chr7:6761698..6764136-chr7:6769053..6770920,2	MCF-7	breast:
4	chr7:6745224..6747442-chr7:6767898..6770902,3	MCF-7	breast:
5	chr7:6767588..6769922-chr7:6774691..6777140,2	MCF-7	breast:
6	chr7:6766860..6769459-chr7:6864426..6866111,2	MCF-7	breast:
7	chr7:6755281..6757989-chr7:6768169..6769805,2	K562	blood:
8	chr7:6745105..6747702-chr7:6760857..6762901,2	MCF-7	breast:
9	chr7:6746161..6747688-chr7:6768318..6771249,2	MCF-7	breast:
10	chr7:6768428..6771621-chr7:6773707..6775724,3	MCF-7	breast:
11	chr7:6745463..6748475-chr7:6767656..6769994,3	K562	blood:
12	chr7:6616941..6618678-chr7:6767339..6769412,2	MCF-7	breast:

(count:4 , 50 per page) page: 1

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-RSPH10B2-1	chr7:6749757-6749869	NONHSAT119063
4	lnc-AC073343.1-1	chr7:6751010-6751133	NONHSAT119061

No data

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

Extended variants
information (count: 976 )
Associated
traits (count: 77 )

Variant overlapped rSNPs/rCNVs (count:976 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs551771540	chr7:6749266-6749267	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs6463577	chr7:6749311-6749312	Weak transcription Active TSS Enhancers	TF binding region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs548071423	chr7:6749316-6749317	Weak transcription Active TSS Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
4	rs188150500	chr7:6749317-6749318	Weak transcription Active TSS Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
5	rs377733446	chr7:6749333-6749334	Weak transcription Active TSS Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
6	rs546182701	chr7:6749340-6749341	Weak transcription Active TSS Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
7	rs7799568	chr7:6749391-6749392	Weak transcription Active TSS Enhancers	TF binding region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs144083255	chr7:6749437-6749438	Weak transcription Active TSS Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
9	rs570140887	chr7:6749443-6749444	Weak transcription Active TSS Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
10	rs531009667	chr7:6749455-6749456	Weak transcription Active TSS Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
11	rs531058952	chr7:6749460-6749461	Weak transcription Active TSS Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
12	rs148243030	chr7:6749483-6749484	Weak transcription Active TSS Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
13	rs549541452	chr7:6749497-6749498	Weak transcription Active TSS Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
14	rs561486015	chr7:6749498-6749499	Weak transcription Active TSS Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
15	rs10259284	chr7:6749499-6749500	Weak transcription Active TSS Enhancers	TF binding region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs141377545	chr7:6749530-6749531	Weak transcription Active TSS Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
17	rs118061061	chr7:6749542-6749543	Weak transcription Active TSS Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
18	rs539642462	chr7:6749555-6749556	Weak transcription Active TSS Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
19	rs534471906	chr7:6749596-6749597	Weak transcription Active TSS Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
20	rs557696646	chr7:6749633-6749634	Weak transcription ZNF genes & repeats Enhancers Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
21	rs528962838	chr7:6749690-6749691	Weak transcription ZNF genes & repeats Enhancers Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
22	rs6967414	chr7:6749758-6749759	Weak transcription ZNF genes & repeats Enhancers Active TSS	TF binding region lncRNA	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
23	rs190401305	chr7:6749835-6749836	ZNF genes & repeats Weak transcription Flanking Active TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
24	rs147421645	chr7:6749843-6749844	ZNF genes & repeats Weak transcription Flanking Active TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
25	rs573309467	chr7:6749871-6749872	ZNF genes & repeats Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs373646392	chr7:6749917-6749918	ZNF genes & repeats Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs541327991	chr7:6749941-6749942	ZNF genes & repeats Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs530355696	chr7:6749946-6749947	ZNF genes & repeats Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs560016868	chr7:6749988-6749989	ZNF genes & repeats Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs533483201	chr7:6750004-6750005	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs139463322	chr7:6750010-6750011	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs144976412	chr7:6750011-6750012	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs139267889	chr7:6750051-6750052	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs375140212	chr7:6750054-6750055	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs531025953	chr7:6750063-6750064	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs183000736	chr7:6750066-6750067	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs548450289	chr7:6750067-6750068	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs528505222	chr7:6750094-6750095	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs547346897	chr7:6750107-6750108	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs6969066	chr7:6750112-6750113	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs187603751	chr7:6750131-6750132	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs557925158	chr7:6750156-6750157	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs569516654	chr7:6750187-6750188	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs112313126	chr7:6750265-6750266	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs147138566	chr7:6750273-6750274	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs192586779	chr7:6750279-6750280	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs573274281	chr7:6750317-6750318	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs140443169	chr7:6750319-6750320	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs552725290	chr7:6750334-6750335	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs538570033	chr7:6750343-6750344	Weak transcription Enhancers	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:65 , 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	chr7:6747200-6749600	Weak transcription	H9 Cell Line	embryonic stem cell
3	chr7:6747400-6750600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
4	chr7:6747400-6752600	Weak transcription	HSMMtube	muscle
5	chr7:6747400-6757400	Weak transcription	Fetal Brain Female	brain
6	chr7:6748000-6749800	Active TSS	Liver	Liver
7	chr7:6748200-6749600	Enhancers	HepG2	liver
8	chr7:6749000-6749800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr7:6749600-6749800	Enhancers	Primary T killer memory cells from peripheral blood	blood
10	chr7:6749600-6750000	ZNF genes & repeats	H9 Cell Line	embryonic stem cell
11	chr7:6749800-6750000	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr7:6749800-6750000	Flanking Active TSS	Liver	Liver
13	chr7:6750000-6750400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr7:6750000-6750600	Enhancers	Liver	Liver
15	chr7:6750600-6752200	Weak transcription	Liver	Liver
16	chr7:6752200-6754600	Strong transcription	Liver	Liver
17	chr7:6754600-6768600	Weak transcription	Liver	Liver
18	chr7:6759400-6759600	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
19	chr7:6763600-6766600	Enhancers	Primary B cells from cord blood	blood
20	chr7:6764000-6765800	Enhancers	Primary hematopoietic stem cells short term culture	blood
21	chr7:6764000-6766200	Enhancers	Primary B cells from peripheral blood	blood
22	chr7:6764200-6764600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
23	chr7:6764200-6765800	Enhancers	Primary hematopoietic stem cells	blood
24	chr7:6764200-6766200	Enhancers	GM12878-XiMat	blood
25	chr7:6764400-6765200	Enhancers	Primary neutrophils fromperipheralblood	blood
26	chr7:6764400-6765400	Enhancers	Primary monocytes fromperipheralblood	blood
27	chr7:6764400-6765800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
28	chr7:6764600-6764800	Enhancers	ES-I3 Cell Line	embryonic stem cell
29	chr7:6764600-6764800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
30	chr7:6764600-6764800	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
31	chr7:6764600-6765200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
32	chr7:6764600-6765200	Enhancers	Spleen	Spleen
33	chr7:6764600-6765800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
34	chr7:6764800-6765000	Enhancers	Monocytes-CD14+_RO01746	blood
35	chr7:6765000-6765200	Enhancers	Sigmoid Colon	Sigmoid Colon
36	chr7:6765000-6768600	Weak transcription	Monocytes-CD14+_RO01746	blood
37	chr7:6765200-6765800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
38	chr7:6765200-6766000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
39	chr7:6765200-6768600	Weak transcription	Primary neutrophils fromperipheralblood	blood
40	chr7:6765200-6769000	Weak transcription	Spleen	Spleen
41	chr7:6765400-6768600	Weak transcription	Sigmoid Colon	Sigmoid Colon
42	chr7:6765800-6768400	Weak transcription	Primary hematopoietic stem cells	blood
43	chr7:6765800-6768400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
44	chr7:6765800-6768600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
45	chr7:6765800-6768600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
46	chr7:6765800-6768600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
47	chr7:6766000-6766400	Enhancers	NHEK	skin
48	chr7:6766200-6766400	Enhancers	ES-I3 Cell Line	embryonic stem cell
49	chr7:6766200-6766400	Enhancers	Placenta	Placenta
50	chr7:6766200-6768400	Weak transcription	GM12878-XiMat	blood

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