Variant report

Variant	nsv966755
Chromosome Location	chr7:6750289-6769785
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:701)
CpG islands
(count:305)
Chromatin interactive
region (count:15)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:701 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:6769148-6769268	K562	blood:	n/a	n/a
2	ARID3A	chr7:6769330-6769549	HepG2	liver:	n/a	n/a
3	ATF2	chr7:6764660-6765106	GM12878	blood:	n/a	n/a
4	ATF2	chr7:6768932-6769576	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF2	chr7:6765435-6765872	GM12878	blood:	n/a	n/a
6	ATF2	chr7:6764577-6765116	GM12878	blood:	n/a	n/a
7	ATF2	chr7:6769041-6769427	H1-hESC	embryonic stem cell:	n/a	n/a
8	BATF	chr7:6764386-6765017	GM12878	blood:	n/a	n/a
9	BCL11A	chr7:6764490-6765004	GM12878	blood:	n/a	n/a
10	BCL3	chr7:6765434-6765865	GM12878	blood:	n/a	n/a
11	BCL3	chr7:6764602-6765093	GM12878	blood:	n/a	n/a
12	BCLAF1	chr7:6768933-6769605	GM12878	blood:	n/a	chr7:6768960-6768969
13	BCLAF1	chr7:6769053-6769626	GM12878	blood:	n/a	n/a
14	BCLAF1	chr7:6765486-6765849	GM12878	blood:	n/a	n/a
15	BCLAF1	chr7:6764543-6765036	GM12878	blood:	n/a	n/a
16	BHLHE40	chr7:6769137-6769602	GM12878	blood:	n/a	n/a
17	BHLHE40	chr7:6765444-6765862	GM12878	blood:	n/a	n/a
18	BHLHE40	chr7:6769211-6769538	K562	blood:	n/a	n/a
19	BHLHE40	chr7:6764639-6765044	GM12878	blood:	n/a	n/a
20	BRCA1	chr7:6769210-6769550	Hela-S3	cervix:	n/a	n/a
21	BRCA1	chr7:6769345-6769648	HepG2	liver:	n/a	n/a
22	CBX3	chr7:6768879-6769361	K562	blood:	n/a	n/a
23	CBX3	chr7:6768880-6769635	K562	blood:	n/a	n/a
24	CCNT2	chr7:6769175-6769724	K562	blood:	n/a	n/a
25	CHD1	chr7:6769255-6769940	GM12878	blood:	n/a	n/a
26	CHD1	chr7:6764785-6765290	GM12878	blood:	n/a	n/a
27	CHD2	chr7:6769061-6769581	H1-hESC	embryonic stem cell:	n/a	n/a
28	CHD2	chr7:6769097-6769650	GM12878	blood:	n/a	n/a
29	CHD2	chr7:6769156-6770092	K562	blood:	n/a	n/a
30	CHD2	chr7:6769152-6769942	Hela-S3	cervix:	n/a	n/a
31	CHD2	chr7:6769108-6770024	HepG2	liver:	n/a	n/a
32	CREB1	chr7:6769195-6769646	A549	lung:	n/a	n/a
33	CREB1	chr7:6769086-6769579	H1-hESC	embryonic stem cell:	n/a	n/a
34	CREB1	chr7:6769002-6769580	H1-hESC	embryonic stem cell:	n/a	n/a
35	CTCF	chr7:6757962-6757964	MCF-7	breast:	n/a	n/a
36	CTCF	chr7:6769440-6769590	GM12866	blood:	n/a	n/a
37	CTCF	chr7:6759080-6759230	GM12873	blood:	n/a	chr7:6759175-6759184
38	CTCF	chr7:6769540-6769690	A549	lung:	n/a	n/a
39	CTCF	chr7:6769260-6769410	GM12869	blood:	n/a	n/a
40	CTCF	chr7:6757918-6757987	MCF-7	breast:	n/a	chr7:6757947-6757965
41	CTCF	chr7:6764666-6764687	GM12891	blood:	n/a	n/a
42	CTCF	chr7:6756056-6756116	GM20000	blood:	n/a	n/a
43	CTCF	chr7:6769400-6769550	HCFaa	heart:	n/a	n/a
44	CTCF	chr7:6757880-6758030	AG10803	skin:	n/a	chr7:6757947-6757965
45	CTCF	chr7:6764651-6764777	GM12892	blood:	n/a	n/a
46	CTCF	chr7:6769360-6769510	HBMEC	blood vessel:	n/a	n/a
47	CTCF	chr7:6769487-6769544	Pancreas_OC	pancreas:	n/a	n/a
48	CTCF	chr7:6757920-6758070	GM12872	blood:	n/a	chr7:6757947-6757965
49	CTCF	chr7:6769340-6769490	GM12878	blood:	n/a	n/a
50	CTCF	chr7:6769240-6769390	HCM	heart:	n/a	n/a

(count:305 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:6769322-6769372	HepG2	liver:	n/a
2	chr7:6750462-6750512	SK-N-SH_RA	brain:	n/a
3	chr7:6769406-6769456	Hela-S3	cervix:	n/a
4	chr7:6766092-6766142	LNCaP	prostate:	n/a
5	chr7:6769322-6769372	HNPCEpiC	eye:	n/a
6	chr7:6769322-6769372	HIPEpiC	eye:	n/a
7	chr7:6766092-6766142	SK-N-SH_RA	brain:	n/a
8	chr7:6750462-6750512	HRPEpiC	eye:	n/a
9	chr7:6769409-6769459	AoSMC	blood vessel:	n/a
10	chr7:6769406-6769456	K562	blood:	n/a
11	chr7:6769409-6769459	HEEpiC	esophagus:	n/a
12	chr7:6769406-6769456	ECC-1	luminal epithelium:	n/a
13	chr7:6766092-6766142	HRE	kidney:	n/a
14	chr7:6769322-6769372	HCPEpiC	choroid plexus:	n/a
15	chr7:6766092-6766142	HUVEC	blood vessel:	n/a
16	chr7:6769322-6769372	AG09309	skin:	n/a
17	chr7:6750462-6750512	GM12892	blood:	n/a
18	chr7:6769409-6769459	SKMC	muscle:	n/a
19	chr7:6766092-6766142	HIPEpiC	eye:	n/a
20	chr7:6769409-6769459	HCM	heart:	n/a
21	chr7:6769406-6769456	HRCEpiC	kidney:	n/a
22	chr7:6750462-6750512	HCPEpiC	choroid plexus:	n/a
23	chr7:6769409-6769459	PANC-1	pancreas:	n/a
24	chr7:6769409-6769459	HUVEC	blood vessel:	n/a
25	chr7:6769409-6769459	AG04450	lung:	fetal
26	chr7:6750462-6750512	AG09309	skin:	n/a
27	chr7:6769406-6769456	AG04450	lung:	fetal
28	chr7:6766092-6766142	CMK	blood:	n/a
29	chr7:6769406-6769456	HAEpiC	amniotic membrane:	n/a
30	chr7:6769406-6769456	AG04449	skin:	fetal
31	chr7:6750462-6750512	LNCaP	prostate:	n/a
32	chr7:6766092-6766142	ECC-1	luminal epithelium:	n/a
33	chr7:6750462-6750512	HAEpiC	amniotic membrane:	n/a
34	chr7:6766092-6766142	HepG2	liver:	n/a
35	chr7:6766092-6766142	HNPCEpiC	eye:	n/a
36	chr7:6769406-6769456	U87	brain:	n/a
37	chr7:6766092-6766142	SKMC	muscle:	n/a
38	chr7:6769406-6769456	T-47D	breast:	n/a
39	chr7:6769409-6769459	HRCEpiC	kidney:	n/a
40	chr7:6769406-6769456	HPAEpiC	pulmonary alveolar:	n/a
41	chr7:6769409-6769459	U87	brain:	n/a
42	chr7:6769322-6769372	AG04449	skin:	fetal
43	chr7:6769406-6769456	SAEC	small airway:	n/a
44	chr7:6750462-6750512	HUVEC	blood vessel:	n/a
45	chr7:6750462-6750512	GM06990	blood:	n/a
46	chr7:6750462-6750512	IMR90	lung:	fetal
47	chr7:6769322-6769372	AG09319	gingival:	n/a
48	chr7:6750462-6750512	HRE	kidney:	n/a
49	chr7:6769406-6769456	NHBE	bronchial:	n/a
50	chr7:6769322-6769372	NB4	blood:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr7:6746161..6747688-chr7:6768318..6771249,2	MCF-7	breast:
2	chr7:6745463..6748475-chr7:6767656..6769994,3	K562	blood:
3	chr7:6745040..6747820-chr7:6753016..6755979,2	K562	blood:
4	chr7:6767588..6769922-chr7:6774691..6777140,2	MCF-7	breast:
5	chr7:6761698..6764136-chr7:6769053..6770920,2	MCF-7	breast:
6	chr7:6755281..6757989-chr7:6768169..6769805,2	K562	blood:
7	chr7:6675529..6677980-chr7:6768487..6770695,2	K562	blood:
8	chr7:6745224..6747442-chr7:6767898..6770902,3	MCF-7	breast:
9	chr7:6768428..6771621-chr7:6773707..6775724,3	MCF-7	breast:
10	chr7:6048395..6048947-chr7:6768981..6769924,2	NB4	blood:
11	chr7:6616941..6618678-chr7:6767339..6769412,2	MCF-7	breast:
12	chr7:6745105..6747702-chr7:6760857..6762901,2	MCF-7	breast:
13	chr7:6744871..6747873-chr7:6767656..6771321,4	K562	blood:
14	chr2:85554880..85555877-chr7:6769205..6770035,2	Hela-S3	cervix:
15	chr7:6766860..6769459-chr7:6864426..6866111,2	MCF-7	breast:

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

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

No data

Variant related genes	Relation type
ZNF12	TF binding region
PMS2CL	TF binding region
ZNF12	CpG island
PMS2CL	CpG island
ENSG00000205903	chromatin interactions
ENSG00000152291	chromatin interactions
ENSG00000164631	chromatin interactions
ENSG00000136247	chromatin interactions
ENSG00000187953	chromatin interactions
ENSG00000146574	chromatin interactions
ENSG00000106305	chromatin interactions
ENSG00000122512	chromatin interactions

Extended variants
information (count: 1017 )
Associated
traits (count: 77 )

Variant overlapped rSNPs/rCNVs (count:1017 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs573274281	chr7:6750317-6750318	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs140443169	chr7:6750319-6750320	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs552725290	chr7:6750334-6750335	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs538570033	chr7:6750343-6750344	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs556519619	chr7:6750367-6750368	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs112776876	chr7:6750377-6750378	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs184119581	chr7:6750393-6750394	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
8	rs541700631	chr7:6750395-6750396	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
9	rs550603266	chr7:6750447-6750448	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs568978817	chr7:6750448-6750449	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs187906123	chr7:6750452-6750453	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs543113032	chr7:6750462-6750463	Weak transcription Enhancers	CpG island	1 gene(s)	Overlapped CNVs	n/a
13	rs374074862	chr7:6750469-6750470	Weak transcription Enhancers	CpG island	1 gene(s)	Overlapped CNVs	n/a
14	rs77714679	chr7:6750494-6750495	Weak transcription Enhancers	CpG island	1 gene(s)	Overlapped CNVs	n/a
15	rs370268577	chr7:6750534-6750535	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs546957203	chr7:6750535-6750536	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs60514449	chr7:6750543-6750544	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs533254097	chr7:6750554-6750555	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs554194307	chr7:6750564-6750565	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs368845283	chr7:6750580-6750581	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs149688386	chr7:6750589-6750590	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs192491132	chr7:6750603-6750604	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs536867889	chr7:6750614-6750615	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs548792719	chr7:6750624-6750625	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs567336186	chr7:6750630-6750631	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs534458354	chr7:6750632-6750633	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs112806901	chr7:6750658-6750659	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs552928601	chr7:6750700-6750701	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs145367027	chr7:6750734-6750735	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs184873585	chr7:6750748-6750749	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs376524279	chr7:6750777-6750778	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs557705724	chr7:6750790-6750791	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs188787807	chr7:6750793-6750794	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs149183701	chr7:6750821-6750822	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs371416829	chr7:6750822-6750823	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs142466716	chr7:6750870-6750871	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs540419641	chr7:6750898-6750899	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs117224366	chr7:6750900-6750901	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs532416885	chr7:6750903-6750904	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs76391602	chr7:6750906-6750907	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs563220910	chr7:6750918-6750919	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs530745368	chr7:6750921-6750922	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs548754811	chr7:6750922-6750923	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs567393094	chr7:6750942-6750943	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs116188688	chr7:6750946-6750947	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs535641332	chr7:6750952-6750953	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs181551910	chr7:6750961-6750962	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs571191004	chr7:6751001-6751002	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs184606004	chr7:6751032-6751033	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
50	rs115037396	chr7:6751053-6751054	Weak transcription	lncRNA	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:262 , 50 per page) page: 1 2 3 4 5 6

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	chr7:6750000-6750400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr7:6750000-6750600	Enhancers	Liver	Liver
7	chr7:6750600-6752200	Weak transcription	Liver	Liver
8	chr7:6752200-6754600	Strong transcription	Liver	Liver
9	chr7:6754600-6768600	Weak transcription	Liver	Liver
10	chr7:6759400-6759600	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
11	chr7:6763600-6766600	Enhancers	Primary B cells from cord blood	blood
12	chr7:6764000-6765800	Enhancers	Primary hematopoietic stem cells short term culture	blood
13	chr7:6764000-6766200	Enhancers	Primary B cells from peripheral blood	blood
14	chr7:6764200-6764600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
15	chr7:6764200-6765800	Enhancers	Primary hematopoietic stem cells	blood
16	chr7:6764200-6766200	Enhancers	GM12878-XiMat	blood
17	chr7:6764400-6765200	Enhancers	Primary neutrophils fromperipheralblood	blood
18	chr7:6764400-6765400	Enhancers	Primary monocytes fromperipheralblood	blood
19	chr7:6764400-6765800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
20	chr7:6764600-6764800	Enhancers	ES-I3 Cell Line	embryonic stem cell
21	chr7:6764600-6764800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
22	chr7:6764600-6764800	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
23	chr7:6764600-6765200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
24	chr7:6764600-6765200	Enhancers	Spleen	Spleen
25	chr7:6764600-6765800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
26	chr7:6764800-6765000	Enhancers	Monocytes-CD14+_RO01746	blood
27	chr7:6765000-6765200	Enhancers	Sigmoid Colon	Sigmoid Colon
28	chr7:6765000-6768600	Weak transcription	Monocytes-CD14+_RO01746	blood
29	chr7:6765200-6765800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
30	chr7:6765200-6766000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
31	chr7:6765200-6768600	Weak transcription	Primary neutrophils fromperipheralblood	blood
32	chr7:6765200-6769000	Weak transcription	Spleen	Spleen
33	chr7:6765400-6768600	Weak transcription	Sigmoid Colon	Sigmoid Colon
34	chr7:6765800-6768400	Weak transcription	Primary hematopoietic stem cells	blood
35	chr7:6765800-6768400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
36	chr7:6765800-6768600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
37	chr7:6765800-6768600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
38	chr7:6765800-6768600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
39	chr7:6766000-6766400	Enhancers	NHEK	skin
40	chr7:6766200-6766400	Enhancers	ES-I3 Cell Line	embryonic stem cell
41	chr7:6766200-6766400	Enhancers	Placenta	Placenta
42	chr7:6766200-6768400	Weak transcription	GM12878-XiMat	blood
43	chr7:6766200-6768800	Weak transcription	Primary B cells from peripheral blood	blood
44	chr7:6766200-6769000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
45	chr7:6766400-6768600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
46	chr7:6766400-6769000	Weak transcription	NHEK	skin
47	chr7:6766600-6768600	Weak transcription	Primary B cells from cord blood	blood
48	chr7:6766600-6768800	Weak transcription	Placenta	Placenta
49	chr7:6767400-6767600	Enhancers	HSMMtube	muscle
50	chr7:6767400-6767600	Enhancers	K562	blood

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