Variant report

Variant	esv3427026
Chromosome Location	chr7:65336942-65339890
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	BACH1	chr7:65338017-65338205	H1-hESC	embryonic stem cell:	n/a	n/a
2	CCNT2	chr7:65337783-65338592	K562	blood:	n/a	chr7:65338186-65338195
3	CEBPB	chr7:65337762-65338153	IMR90	lung:	n/a	n/a
4	CEBPB	chr7:65337697-65338239	Hela-S3	cervix:	n/a	n/a
5	CEBPB	chr7:65337913-65338272	HepG2	liver:	n/a	n/a
6	CEBPB	chr7:65338012-65338138	A549	lung:	n/a	n/a
7	CEBPB	chr7:65338009-65338209	K562	blood:	n/a	n/a
8	CEBPB	chr7:65338072-65338234	HepG2	liver:	n/a	n/a
9	CEBPD	chr7:65337963-65338299	HepG2	liver:	n/a	n/a
10	CHD1	chr7:65339184-65339363	GM12878	blood:	n/a	n/a
11	CHD1	chr7:65338466-65338502	GM12878	blood:	n/a	n/a
12	CHD2	chr7:65337705-65338547	Hela-S3	cervix:	n/a	n/a
13	CREB1	chr7:65337861-65338372	K562	blood:	n/a	n/a
14	CREB1	chr7:65337827-65338529	HepG2	liver:	n/a	n/a
15	CREB1	chr7:65337935-65338206	H1-hESC	embryonic stem cell:	n/a	n/a
16	CREB1	chr7:65337864-65338263	A549	lung:	n/a	n/a
17	E2F1	chr7:65337902-65338279	Hela-S3	cervix:	n/a	chr7:65338132-65338144 chr7:65338186-65338195 chr7:65338116-65338125
18	E2F4	chr7:65337764-65338276	MCF10A-Er-Src	breast:	n/a	chr7:65338132-65338144 chr7:65338186-65338195 chr7:65338116-65338125
19	E2F6	chr7:65337963-65338205	K562	blood:	n/a	chr7:65338132-65338144 chr7:65338186-65338195 chr7:65338116-65338125
20	E2F6	chr7:65337907-65338563	K562	blood:	n/a	chr7:65338132-65338144 chr7:65338186-65338195 chr7:65338116-65338125 chr7:65338466-65338477
21	E2F6	chr7:65337971-65338292	K562	blood:	n/a	chr7:65338132-65338144 chr7:65338186-65338195 chr7:65338116-65338125
22	EBF1	chr7:65337659-65337929	GM12878	blood:	n/a	n/a
23	EBF1	chr7:65337651-65337926	GM12878	blood:	n/a	n/a
24	EGR1	chr7:65337996-65338374	GM12878	blood:	n/a	chr7:65338101-65338116 chr7:65338118-65338127 chr7:65338186-65338196 chr7:65338181-65338194 chr7:65338182-65338196 chr7:65338184-65338194 chr7:65338004-65338014
25	EGR1	chr7:65338685-65338951	K562	blood:	n/a	chr7:65338930-65338940
26	EGR1	chr7:65337961-65338447	K562	blood:	n/a	chr7:65338101-65338116 chr7:65338118-65338127 chr7:65338186-65338196 chr7:65338181-65338194 chr7:65338182-65338196 chr7:65338184-65338194 chr7:65338004-65338014
27	EGR1	chr7:65337949-65338441	K562	blood:	n/a	chr7:65338101-65338116 chr7:65338118-65338127 chr7:65338186-65338196 chr7:65338181-65338194 chr7:65338182-65338196 chr7:65338184-65338194 chr7:65338004-65338014
28	EGR1	chr7:65338003-65338254	GM12878	blood:	n/a	chr7:65338101-65338116 chr7:65338118-65338127 chr7:65338186-65338196 chr7:65338181-65338194 chr7:65338182-65338196 chr7:65338184-65338194 chr7:65338004-65338014
29	EGR1	chr7:65337843-65338454	HCT-116	colon:	n/a	chr7:65338101-65338116 chr7:65338118-65338127 chr7:65338186-65338196 chr7:65338181-65338194 chr7:65338182-65338196 chr7:65338184-65338194 chr7:65338004-65338014
30	EGR1	chr7:65339298-65339537	K562	blood:	n/a	n/a
31	ELF1	chr7:65337990-65338235	K562	blood:	n/a	chr7:65338190-65338202
32	ELF1	chr7:65338424-65338606	K562	blood:	n/a	n/a
33	ELF1	chr7:65338716-65339143	GM12878	blood:	n/a	n/a
34	EP300	chr7:65338052-65338110	K562	blood:	n/a	chr7:65338066-65338082
35	EP300	chr7:65337989-65338211	T-47D	breast:	n/a	chr7:65338030-65338046 chr7:65338066-65338082 chr7:65338116-65338125
36	EP300	chr7:65337923-65338199	HepG2	liver:	n/a	chr7:65338030-65338046 chr7:65338066-65338082 chr7:65338116-65338125
37	EP300	chr7:65337994-65338232	SK-N-SH_RA	brain:	n/a	chr7:65338030-65338046 chr7:65338066-65338082 chr7:65338116-65338125
38	EP300	chr7:65338054-65338614	ECC-1	luminal epithelium:	n/a	chr7:65338066-65338082 chr7:65338116-65338125
39	ETS1	chr7:65337964-65338137	K562	blood:	n/a	chr7:65338064-65338075
40	ETS1	chr7:65338286-65338583	K562	blood:	n/a	n/a
41	FOS	chr7:65337712-65337888	MCF10A-Er-Src	breast:	n/a	n/a
42	FOS	chr7:65337786-65337903	MCF10A-Er-Src	breast:	n/a	n/a
43	FOS	chr7:65337703-65337867	MCF10A-Er-Src	breast:	n/a	n/a
44	FOSL2	chr7:65337635-65338033	HepG2	liver:	n/a	n/a
45	FOXP2	chr7:65337987-65338186	SK-N-MC	brain:	n/a	n/a
46	GTF3C2	chr7:65339159-65339631	K562	blood:	n/a	n/a
47	GTF3C2	chr7:65339161-65339519	Hela-S3	cervix:	n/a	n/a
48	HA-E2F1	chr7:65337867-65338467	Hela-S3	cervix:	n/a	chr7:65338132-65338144 chr7:65338186-65338195 chr7:65338116-65338125
49	HCFC1	chr7:65338037-65338227	K562	blood:	n/a	n/a
50	HDAC2	chr7:65338313-65338566	K562	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:65337924-65337974	SAEC	small airway:	n/a
2	chr7:65337924-65337974	SAEC	small airway:	n/a
3	chr7:65338708-65338758	NB4	blood:	n/a
4	chr7:65337895-65337945	AG10803	skin:	n/a
5	chr7:65338055-65338105	NH-A	brain:	n/a
6	chr7:65338427-65338477	SAEC	small airway:	n/a
7	chr7:65338427-65338477	NHDF-neo	bronchial:	n/a
8	chr7:65337895-65337945	NHBE	bronchial:	n/a
9	chr7:65337924-65337974	Hela-S3	cervix:	n/a
10	chr7:65338708-65338758	NH-A	brain:	n/a
11	chr7:65338708-65338758	NHBE	bronchial:	n/a
12	chr7:65337895-65337945	NB4	blood:	n/a
13	chr7:65337924-65337974	HRE	kidney:	n/a
14	chr7:65337924-65337974	AG04450	lung:	fetal
15	chr7:65338716-65338766	AG09309	skin:	n/a
16	chr7:65337895-65337945	AG09319	gingival:	n/a
17	chr7:65338708-65338758	K562	blood:	n/a
18	chr7:65338427-65338477	HMEC	breast:	n/a
19	chr7:65337895-65337945	SK-N-MC	brain:	n/a
20	chr7:65338427-65338477	SK-N-SH_RA	brain:	n/a
21	chr7:65338427-65338477	U87	brain:	n/a
22	chr7:65338716-65338766	MCF10A-Er-Src	breast:	n/a
23	chr7:65337895-65337945	PANC-1	pancreas:	n/a
24	chr7:65338055-65338105	HCF	heart:	n/a
25	chr7:65338427-65338477	AG09309	skin:	n/a
26	chr7:65337895-65337945	ovcar-3	ovarian:	n/a
27	chr7:65337924-65337974	GM06990	blood:	n/a
28	chr7:65338708-65338758	IMR90	lung:	fetal
29	chr7:65337924-65337974	HMEC	breast:	n/a
30	chr7:65338427-65338477	HPAEpiC	pulmonary alveolar:	n/a
31	chr7:65338055-65338105	K562	blood:	n/a
32	chr7:65338716-65338766	HRE	kidney:	n/a
33	chr7:65337895-65337945	HNPCEpiC	eye:	n/a
34	chr7:65338055-65338105	HMEC	breast:	n/a
35	chr7:65338716-65338766	AG04450	lung:	fetal
36	chr7:65337895-65337945	ECC-1	luminal epithelium:	n/a
37	chr7:65337924-65337974	Caco-2	colon:	n/a
38	chr7:65338716-65338766	HNPCEpiC	eye:	n/a
39	chr7:65337895-65337945	A549	lung:	n/a
40	chr7:65338055-65338105	HepG2	liver:	n/a
41	chr7:65338055-65338105	Hepatocyte	liver:	n/a
42	chr7:65337924-65337974	SK-N-SH_RA	brain:	n/a
43	chr7:65338708-65338758	HCM	heart:	n/a
44	chr7:65338716-65338766	ProgFib	skin:	n/a
45	chr7:65338708-65338758	GM12892	blood:	n/a
46	chr7:65338708-65338758	GM19239	blood:	n/a
47	chr7:65337895-65337945	GM06990	blood:	n/a
48	chr7:65337895-65337945	HCT-116	colon:	n/a
49	chr7:65338427-65338477	H1-hESC	embryonic stem cell:	embryo
50	chr7:65337895-65337945	GM19239	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr7:64498559..64499288-chr7:65338067..65339051,2	NB4	blood:
2	chr7:65214366..65217502-chr7:65337041..65339664,3	MCF-7	breast:
3	chr7:64498619..64500351-chr7:65337220..65338727,3	MCF-7	breast:
4	chr7:65337864..65339398-chr7:65445758..65448693,2	K562	blood:
5	chr11:62609016..62609720-chr7:65338341..65338852,2	Hela-S3	cervix:

Variant related genes	Relation type
VKORC1L1	TF binding region
VKORC1L1	CpG island
ENSG00000234585	chromatin interactions
ENSG00000169919	chromatin interactions
ENSG00000133316	chromatin interactions
ENSG00000239985	chromatin interactions
ENSG00000228409	chromatin interactions

Extended variants
information (count: 99 )
Associated
traits (count: 77 )

Variant overlapped rSNPs/rCNVs (count:99 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs559151277	chr7:65337018-65337019	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs555739359	chr7:65337081-65337082	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs10259772	chr7:65337133-65337134	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs575804555	chr7:65337139-65337140	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs571247977	chr7:65337171-65337172	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs376126458	chr7:65337196-65337197	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs530566833	chr7:65337261-65337262	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
8	rs551248905	chr7:65337300-65337301	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
9	rs544445519	chr7:65337310-65337311	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
10	rs369691304	chr7:65337313-65337314	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
11	rs536807070	chr7:65337314-65337315	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
12	rs200307884	chr7:65337321-65337322	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
13	rs563071333	chr7:65337331-65337332	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
14	rs566979538	chr7:65337339-65337340	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
15	rs137968395	chr7:65337349-65337350	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
16	rs558823258	chr7:65337376-65337377	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
17	rs575233092	chr7:65337393-65337394	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
18	rs544204654	chr7:65337399-65337400	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
19	rs144006459	chr7:65337400-65337401	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
20	rs373582453	chr7:65337460-65337461	Enhancers Weak transcription Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
21	rs189438351	chr7:65337503-65337504	Enhancers Weak transcription Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
22	rs180985581	chr7:65337576-65337577	Enhancers Weak transcription Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
23	rs545432694	chr7:65337600-65337601	Enhancers Flanking Active TSS Active TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
24	rs111369389	chr7:65337647-65337648	Flanking Active TSS Enhancers Active TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
25	rs558919905	chr7:65337717-65337718	Flanking Active TSS Enhancers Active TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
26	rs184886728	chr7:65337769-65337770	Flanking Active TSS Enhancers Active TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
27	rs528309801	chr7:65337800-65337801	Flanking Active TSS Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
28	rs545084019	chr7:65337850-65337851	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
29	rs564974062	chr7:65337853-65337854	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
30	rs375918409	chr7:65337855-65337856	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
31	rs376204057	chr7:65337887-65337888	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
32	rs55773927	chr7:65337902-65337903	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region CpG island Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
33	rs561534392	chr7:65337953-65337954	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
34	rs551718785	chr7:65337973-65337974	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
35	rs190926740	chr7:65337976-65337977	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	mRNA abundance
36	rs547010692	chr7:65337980-65337981	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
37	rs181846215	chr7:65337993-65337994	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
38	rs186038541	chr7:65338208-65338209	Active TSS Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
39	rs567043699	chr7:65338242-65338243	Active TSS Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
40	rs191736197	chr7:65338244-65338245	Active TSS Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
41	rs371974807	chr7:65338271-65338272	Active TSS Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
42	rs538912415	chr7:65338337-65338338	Active TSS Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
43	rs552596206	chr7:65338370-65338371	Active TSS Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
44	rs569022825	chr7:65338418-65338419	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
45	rs148752040	chr7:65338421-65338422	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
46	rs537816630	chr7:65338433-65338434	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
47	rs554566229	chr7:65338445-65338446	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
48	rs374961625	chr7:65338463-65338464	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
49	rs373575875	chr7:65338491-65338492	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
50	rs536532694	chr7:65338564-65338565	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:77)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17170743	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	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
Melanoma	18172304	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	22495311	CNVD
Follicular lymphoma	20505157	CNVD
Biliary cancer	19435499	CNVD
Williams-beuren syndrome	22470819	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Multiple myeloma	16461302	CNVD
Glioblastoma multiforme	21750150	CNVD
Cancer	21183584	CNVD
Hepatocellular carcinoma	16750200	CNVD
Non-small cell lung cancer	21829676	CNVD
Gastric cancer	24379144	CNVD
Glioblastoma multiforme	17002787	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Lissencephaly	21572526	CNVD
Breast cancer	17603634	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	16397240	CNVD
Acute myeloid leukemia	16864856	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Squamous cell cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Glioblastoma multiforme	17387387	CNVD
Low-grade fibromyxoid sarcoma	0	CNVD
Oligodendroglial tumors	17285580	CNVD
Endometrial cancer	22040021	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	21264507	CNVD
Shwachman-Diamond syndrome	22934832	CNVD
Glioblastoma	21080181	CNVD
Colorectal cancer	19359472	CNVD
Cutaneous malignant melanoma	17690212	CNVD
Leukemia	17361228	CNVD
Breast cancer	16461572	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Malignant melanoma	17690212	CNVD
Breast cancer	21990379	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	21399695	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Astrocytoma	22246337	CNVD
Renal cell carcinoma	18592004	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21364760	CNVD
Acute monocytic leukemia	16498392	CNVD
Prostate cancer	16461572	CNVD
Salivary gland tumor	18059337	CNVD
Multiple myeloma	17550852	CNVD
Acute myeloid leukemia	21251322	CNVD
small cell lung cancer	20016488	CNVD
Bladder cancer	21909424	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Melanoma	20877625	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:367 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:65330800-65338200	Weak transcription	Right Atrium	heart
2	chr7:65334600-65338400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
3	chr7:65334800-65337400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
4	chr7:65334800-65337800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
5	chr7:65334800-65338200	Weak transcription	NHLF	lung
6	chr7:65335800-65337600	Enhancers	Adipose Nuclei	Adipose
7	chr7:65335800-65338000	Enhancers	Primary monocytes fromperipheralblood	blood
8	chr7:65335800-65338000	Enhancers	Primary hematopoietic stem cells short term culture	blood
9	chr7:65336000-65338400	Weak transcription	Primary B cells from cord blood	blood
10	chr7:65336200-65338000	Enhancers	Primary neutrophils fromperipheralblood	blood
11	chr7:65336400-65337400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
12	chr7:65336600-65337600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
13	chr7:65336600-65337600	Enhancers	NHDF-Ad	bronchial
14	chr7:65336600-65337800	Enhancers	GM12878-XiMat	blood
15	chr7:65336600-65338000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
16	chr7:65336600-65338200	Weak transcription	Fetal Muscle Trunk	muscle
17	chr7:65336800-65337200	Enhancers	Monocytes-CD14+_RO01746	blood
18	chr7:65336800-65338200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
19	chr7:65337000-65337600	Weak transcription	HUVEC	blood vessel
20	chr7:65337200-65337400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
21	chr7:65337200-65337400	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
22	chr7:65337200-65337600	Enhancers	K562	blood
23	chr7:65337400-65337600	Enhancers	H1 Cell Line	embryonic stem cell
24	chr7:65337400-65337600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
25	chr7:65337400-65337600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
26	chr7:65337400-65337600	Enhancers	Left Ventricle	heart
27	chr7:65337400-65337600	Enhancers	Thymus	Thymus
28	chr7:65337400-65337600	Enhancers	Dnd41	blood
29	chr7:65337400-65337600	Enhancers	HepG2	liver
30	chr7:65337400-65337600	Weak transcription	HSMMtube	muscle
31	chr7:65337400-65337600	Enhancers	Monocytes-CD14+_RO01746	blood
32	chr7:65337400-65337800	Enhancers	Placenta	Placenta
33	chr7:65337400-65337800	Enhancers	Skeletal Muscle Male	skeletal muscle
34	chr7:65337400-65337800	Enhancers	NHEK	skin
35	chr7:65337400-65338000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
36	chr7:65337400-65338000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
37	chr7:65337400-65338000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
38	chr7:65337400-65338000	Enhancers	Muscle Satellite Cultured Cells	--
39	chr7:65337400-65338000	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
40	chr7:65337400-65338000	Enhancers	Fetal Muscle Leg	muscle
41	chr7:65337400-65338000	Enhancers	Skeletal Muscle Female	skeletal muscle
42	chr7:65337400-65338200	Enhancers	Primary T cells fromperipheralblood	blood
43	chr7:65337400-65339200	Active TSS	Hela-S3	cervix
44	chr7:65337400-65339600	Active TSS	A549	lung
45	chr7:65337600-65337800	Flanking Active TSS	H1 Cell Line	embryonic stem cell
46	chr7:65337600-65337800	Enhancers	Primary T killer memory cells from peripheral blood	blood
47	chr7:65337600-65337800	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
48	chr7:65337600-65337800	Flanking Active TSS	Adipose Nuclei	Adipose
49	chr7:65337600-65337800	Enhancers	Liver	Liver
50	chr7:65337600-65337800	Enhancers	Brain Germinal Matrix	brain

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