Variant report

Variant	nsv8039
Chromosome Location	chr7:6748111-6764886
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:258)
CpG islands
(count:123)
Chromatin interactive
region (count:7)
LncRNA
region (count:7)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:258 , 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	ARID3A	chr7:6747987-6748210	HepG2	liver:	n/a	n/a
3	ATF2	chr7:6764577-6765116	GM12878	blood:	n/a	n/a
4	ATF2	chr7:6764660-6765106	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	BCLAF1	chr7:6764543-6765036	GM12878	blood:	n/a	n/a
9	BHLHE40	chr7:6764639-6765044	GM12878	blood:	n/a	n/a
10	CBX3	chr7:6749454-6749792	K562	blood:	n/a	n/a
11	CBX3	chr7:6749398-6749899	HCT-116	colon:	n/a	n/a
12	CBX3	chr7:6749453-6749879	K562	blood:	n/a	n/a
13	CHD1	chr7:6764785-6765290	GM12878	blood:	n/a	n/a
14	CHD2	chr7:6749610-6749810	HepG2	liver:	n/a	n/a
15	CTCF	chr7:6757840-6757990	HPF	lung:	n/a	chr7:6757947-6757965
16	CTCF	chr7:6757880-6758030	NHEK	skin:	n/a	chr7:6757947-6757965
17	CTCF	chr7:6757860-6758010	GM12868	blood:	n/a	chr7:6757947-6757965
18	CTCF	chr7:6757900-6758050	HMEC	breast:	n/a	chr7:6757947-6757965
19	CTCF	chr7:6755706-6755761	GM19239	blood:	n/a	n/a
20	CTCF	chr7:6757796-6758103	K562	blood:	n/a	chr7:6757947-6757965
21	CTCF	chr7:6757860-6758010	HCPEpiC	choroid plexus:	n/a	chr7:6757947-6757965
22	CTCF	chr7:6757884-6757994	LNCaP	prostate:	n/a	chr7:6757947-6757965
23	CTCF	chr7:6757880-6758030	NHLF	lung:	n/a	chr7:6757947-6757965
24	CTCF	chr7:6757920-6758070	GM12872	blood:	n/a	chr7:6757947-6757965
25	CTCF	chr7:6757883-6758037	Hela-S3	cervix:	n/a	chr7:6757947-6757965
26	CTCF	chr7:6757898-6758010	NHEK	skin:	n/a	chr7:6757947-6757965
27	CTCF	chr7:6757889-6758040	GM19238	blood:	n/a	chr7:6757947-6757965
28	CTCF	chr7:6764739-6764762	GM19240	blood:	n/a	n/a
29	CTCF	chr7:6757914-6757992	MCF-7	breast:	n/a	chr7:6757947-6757965
30	CTCF	chr7:6757875-6758035	GM10266	blood:	n/a	chr7:6757947-6757965
31	CTCF	chr7:6757880-6758030	HepG2	liver:	n/a	chr7:6757947-6757965
32	CTCF	chr7:6757879-6757999	Medullo	brain:	n/a	chr7:6757947-6757965
33	CTCF	chr7:6757920-6758070	HBMEC	blood vessel:	n/a	chr7:6757947-6757965
34	CTCF	chr7:6757860-6758010	HUVEC	blood vessel:	n/a	chr7:6757947-6757965
35	CTCF	chr7:6757854-6758043	H1-hESC	embryonic stem cell:	n/a	chr7:6757947-6757965
36	CTCF	chr7:6757920-6758070	SAEC	small airway:	n/a	chr7:6757947-6757965
37	CTCF	chr7:6759218-6759243	H1-hESC	embryonic stem cell:	n/a	chr7:6759224-6759237
38	CTCF	chr7:6757840-6757990	GM12869	blood:	n/a	chr7:6757947-6757965
39	CTCF	chr7:6757880-6758030	GM12874	blood:	n/a	chr7:6757947-6757965
40	CTCF	chr7:6764729-6764796	Spleen_OC	spleen:	n/a	n/a
41	CTCF	chr7:6757880-6758030	GM12864	blood:	n/a	chr7:6757947-6757965
42	CTCF	chr7:6757914-6758033	GM12892	blood:	n/a	chr7:6757947-6757965
43	CTCF	chr7:6758160-6758310	GM12873	blood:	n/a	n/a
44	CTCF	chr7:6764672-6764675	GM19238	blood:	n/a	n/a
45	CTCF	chr7:6757920-6758070	HPAF	blood vessel:	n/a	chr7:6757947-6757965
46	CTCF	chr7:6757900-6758050	HMF	breast:	n/a	chr7:6757947-6757965
47	CTCF	chr7:6757920-6758070	HFF-Myc	foreskin:	n/a	chr7:6757947-6757965
48	CTCF	chr7:6757900-6758050	GM12873	blood:	n/a	chr7:6757947-6757965
49	CTCF	chr7:6755722-6755792	K562	blood:	n/a	n/a
50	CTCF	chr7:6757900-6758050	GM12875	blood:	n/a	chr7:6757947-6757965

(count:123 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:6750462-6750512	SK-N-SH	brain:	n/a
2	chr7:6750462-6750512	SK-N-SH	brain:	n/a
3	chr7:6749638-6749688	HL-60	blood:	n/a
4	chr7:6749638-6749688	HEEpiC	esophagus:	n/a
5	chr7:6750462-6750512	U87	brain:	n/a
6	chr7:6749638-6749688	AG09309	skin:	n/a
7	chr7:6749638-6749688	SK-N-SH_RA	brain:	n/a
8	chr7:6749638-6749688	HCM	heart:	n/a
9	chr7:6749638-6749688	MCF10A-Er-Src	breast:	n/a
10	chr7:6750462-6750512	HIPEpiC	eye:	n/a
11	chr7:6749638-6749688	AG04449	skin:	fetal
12	chr7:6750462-6750512	SK-N-MC	brain:	n/a
13	chr7:6749638-6749688	GM12891	blood:	n/a
14	chr7:6749638-6749688	HRPEpiC	eye:	n/a
15	chr7:6749638-6749688	RPTEC	kidney:	n/a
16	chr7:6750462-6750512	SK-N-SH_RA	brain:	n/a
17	chr7:6750462-6750512	HRE	kidney:	n/a
18	chr7:6749638-6749688	HMEC	breast:	n/a
19	chr7:6750462-6750512	SAEC	small airway:	n/a
20	chr7:6749638-6749688	PFSK-1	brain:	n/a
21	chr7:6750462-6750512	HCF	heart:	n/a
22	chr7:6750462-6750512	HCT-116	colon:	n/a
23	chr7:6749638-6749688	Hepatocyte	liver:	n/a
24	chr7:6749638-6749688	SK-N-SH	brain:	n/a
25	chr7:6749638-6749688	NB4	blood:	n/a
26	chr7:6749638-6749688	SKMC	muscle:	n/a
27	chr7:6749638-6749688	Jurkat	blood:	n/a
28	chr7:6749638-6749688	LNCaP	prostate:	n/a
29	chr7:6749638-6749688	HCF	heart:	n/a
30	chr7:6749638-6749688	NT2-D1	testis:	n/a
31	chr7:6750462-6750512	NB4	blood:	n/a
32	chr7:6750462-6750512	GM06990	blood:	n/a
33	chr7:6750462-6750512	Hepatocyte	liver:	n/a
34	chr7:6750462-6750512	HRCEpiC	kidney:	n/a
35	chr7:6749638-6749688	HRCEpiC	kidney:	n/a
36	chr7:6750462-6750512	A549	lung:	n/a
37	chr7:6750462-6750512	RPTEC	kidney:	n/a
38	chr7:6749638-6749688	ovcar-3	ovarian:	n/a
39	chr7:6749638-6749688	GM12878	blood:	n/a
40	chr7:6749638-6749688	HepG2	liver:	n/a
41	chr7:6749638-6749688	Hela-S3	cervix:	n/a
42	chr7:6749638-6749688	T-47D	breast:	n/a
43	chr7:6750462-6750512	NHDF-neo	bronchial:	n/a
44	chr7:6750462-6750512	BJ	skin:	n/a
45	chr7:6749638-6749688	SAEC	small airway:	n/a
46	chr7:6750462-6750512	LNCaP	prostate:	n/a
47	chr7:6750462-6750512	Hela-S3	cervix:	n/a
48	chr7:6750462-6750512	NT2-D1	testis:	n/a
49	chr7:6749638-6749688	GM12892	blood:	n/a
50	chr7:6750462-6750512	ECC-1	luminal epithelium:	n/a

(count:7 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:6729955..6731866-chr7:6746781..6748682,2	MCF-7	breast:
2	chr7:6745105..6747702-chr7:6760857..6762901,2	MCF-7	breast:
3	chr7:6745463..6748475-chr7:6767656..6769994,3	K562	blood:
4	chr7:6681243..6682856-chr7:6746246..6748831,2	K562	blood:
5	chr7:6745040..6747820-chr7:6753016..6755979,2	K562	blood:
6	chr7:6755281..6757989-chr7:6768169..6769805,2	K562	blood:
7	chr7:6761698..6764136-chr7:6769053..6770920,2	MCF-7	breast:

(count:7 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AC073343.1-1	chr7:6751010-6751093	NONHSAT119062
2	lnc-AC073343.1-1	chr7:6748310-6748670	NONHSAT119062
3	lnc-AC073343.1-1	chr7:6746704-6748672	NONHSAT119061
4	lnc-AC073343.1-1	chr7:6750381-6750402	NONHSAT119061
5	lnc-AC073343.1-1	chr7:6751010-6751133	NONHSAT119061
6	lnc-AC073343.1-1	chr7:6748199-6748532	ENSG00000228010.1
7	lnc-RSPH10B2-1	chr7:6749757-6749869	NONHSAT119063

No data

Variant related genes	Relation type
ZNF12	TF binding region
PMS2CL	TF binding region
ZNF12	CpG island
PMS2CL	CpG island
ENSG00000205903	chromatin interactions
ENSG00000187953	chromatin interactions
ENSG00000265245	chromatin interactions
ENSG00000164631	chromatin interactions

Extended variants
information (count: 858 )
Associated
traits (count: 77 )

Variant overlapped rSNPs/rCNVs (count:858 , 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	rs539962387	chr7:6748124-6748125	Weak transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
2	rs557862814	chr7:6748216-6748217	Weak transcription Active TSS Enhancers	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
3	rs576388002	chr7:6748252-6748253	Weak transcription Active TSS Enhancers	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
4	rs3757481	chr7:6748260-6748261	Weak transcription Active TSS Enhancers	TF binding region Chromatin interactive region lncRNA	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs181377394	chr7:6748261-6748262	Weak transcription Active TSS Enhancers	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
6	rs140476914	chr7:6748304-6748305	Weak transcription Active TSS Enhancers	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
7	rs186582342	chr7:6748313-6748314	Weak transcription Active TSS Enhancers	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
8	rs560328628	chr7:6748330-6748331	Weak transcription Active TSS Enhancers	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
9	rs190207890	chr7:6748359-6748360	Weak transcription Active TSS Enhancers	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
10	rs145702951	chr7:6748378-6748379	Weak transcription Active TSS Enhancers	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
11	rs138270682	chr7:6748398-6748399	Weak transcription Active TSS Enhancers	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
12	rs545932790	chr7:6748424-6748425	Weak transcription Active TSS Enhancers	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
13	rs149588569	chr7:6748458-6748459	Weak transcription Active TSS Enhancers	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
14	rs373163651	chr7:6748467-6748468	Weak transcription Active TSS Enhancers	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
15	rs545402064	chr7:6748476-6748477	Weak transcription Active TSS Enhancers	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
16	rs550027251	chr7:6748500-6748501	Weak transcription Active TSS Enhancers	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
17	rs189041536	chr7:6748522-6748523	Weak transcription Active TSS Enhancers	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
18	rs529573147	chr7:6748525-6748526	Weak transcription Active TSS Enhancers	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
19	rs534762851	chr7:6748530-6748531	Weak transcription Active TSS Enhancers	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
20	rs544641551	chr7:6748541-6748542	Weak transcription Active TSS Enhancers	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
21	rs7782227	chr7:6748594-6748595	Weak transcription Active TSS Enhancers	TF binding region Chromatin interactive region lncRNA	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs181752109	chr7:6748618-6748619	Weak transcription Active TSS Enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
23	rs539500950	chr7:6748640-6748641	Weak transcription Active TSS Enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
24	rs551862927	chr7:6748648-6748649	Weak transcription Active TSS Enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
25	rs186370052	chr7:6748669-6748670	Weak transcription Active TSS Enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
26	rs369528898	chr7:6748698-6748699	Weak transcription Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs28361430	chr7:6748739-6748740	Weak transcription Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs560382082	chr7:6748798-6748799	Weak transcription Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs574603766	chr7:6748807-6748808	Weak transcription Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs574766265	chr7:6748828-6748829	Weak transcription Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs542344511	chr7:6748843-6748844	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs180749774	chr7:6748851-6748852	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs186179153	chr7:6748879-6748880	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs373085059	chr7:6748886-6748887	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs191009463	chr7:6748897-6748898	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs528101859	chr7:6748910-6748911	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs3757482	chr7:6748927-6748928	Weak transcription Active TSS Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs3757483	chr7:6748934-6748935	Weak transcription Active TSS Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs575604990	chr7:6748940-6748941	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs200862700	chr7:6748976-6748977	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs183230162	chr7:6749083-6749084	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs370340670	chr7:6749087-6749088	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs533693193	chr7:6749115-6749116	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs575401377	chr7:6749161-6749162	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs374398521	chr7:6749168-6749169	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs551771540	chr7:6749266-6749267	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs6463577	chr7:6749311-6749312	Weak transcription Active TSS Enhancers	TF binding region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs548071423	chr7:6749316-6749317	Weak transcription Active TSS Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
49	rs188150500	chr7:6749317-6749318	Weak transcription Active TSS Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
50	rs377733446	chr7:6749333-6749334	Weak transcription Active TSS Enhancers	TF binding region	2 gene(s)	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:36 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:6747000-6768600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr7:6747200-6748800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr7:6747200-6749600	Weak transcription	H9 Cell Line	embryonic stem cell
4	chr7:6747400-6750600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
5	chr7:6747400-6752600	Weak transcription	HSMMtube	muscle
6	chr7:6747400-6757400	Weak transcription	Fetal Brain Female	brain
7	chr7:6748000-6748200	Flanking Active TSS	HepG2	liver
8	chr7:6748000-6749800	Active TSS	Liver	Liver
9	chr7:6748200-6749600	Enhancers	HepG2	liver
10	chr7:6749000-6749800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr7:6749600-6749800	Enhancers	Primary T killer memory cells from peripheral blood	blood
12	chr7:6749600-6750000	ZNF genes & repeats	H9 Cell Line	embryonic stem cell
13	chr7:6749800-6750000	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr7:6749800-6750000	Flanking Active TSS	Liver	Liver
15	chr7:6750000-6750400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr7:6750000-6750600	Enhancers	Liver	Liver
17	chr7:6750600-6752200	Weak transcription	Liver	Liver
18	chr7:6752200-6754600	Strong transcription	Liver	Liver
19	chr7:6754600-6768600	Weak transcription	Liver	Liver
20	chr7:6759400-6759600	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
21	chr7:6763600-6766600	Enhancers	Primary B cells from cord blood	blood
22	chr7:6764000-6765800	Enhancers	Primary hematopoietic stem cells short term culture	blood
23	chr7:6764000-6766200	Enhancers	Primary B cells from peripheral blood	blood
24	chr7:6764200-6764600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
25	chr7:6764200-6765800	Enhancers	Primary hematopoietic stem cells	blood
26	chr7:6764200-6766200	Enhancers	GM12878-XiMat	blood
27	chr7:6764400-6765200	Enhancers	Primary neutrophils fromperipheralblood	blood
28	chr7:6764400-6765400	Enhancers	Primary monocytes fromperipheralblood	blood
29	chr7:6764400-6765800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
30	chr7:6764600-6764800	Enhancers	ES-I3 Cell Line	embryonic stem cell
31	chr7:6764600-6764800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
32	chr7:6764600-6764800	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
33	chr7:6764600-6765200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
34	chr7:6764600-6765200	Enhancers	Spleen	Spleen
35	chr7:6764600-6765800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
36	chr7:6764800-6765000	Enhancers	Monocytes-CD14+_RO01746	blood

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