Variant report

Variant	nsv607310
Chromosome Location	chr7:63744350-63783386
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:790)
CpG islands
(count:1099)
Chromatin interactive
region (count:26)
LncRNA
region (count:21)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:790 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:63774220-63774596	K562	blood:	n/a	n/a
2	ATF1	chr7:63767585-63768036	K562	blood:	n/a	n/a
3	ATF1	chr7:63774113-63774571	K562	blood:	n/a	n/a
4	ATF2	chr7:63774056-63774556	GM12878	blood:	n/a	n/a
5	ATF2	chr7:63774138-63774662	GM12878	blood:	n/a	n/a
6	ATF2	chr7:63765452-63765906	GM12878	blood:	n/a	n/a
7	BATF	chr7:63757784-63758164	GM12878	blood:	n/a	chr7:63757944-63757955
8	BATF	chr7:63757823-63758057	GM12878	blood:	n/a	chr7:63757944-63757955
9	BCL11A	chr7:63765504-63765813	GM12878	blood:	n/a	chr7:63765624-63765633
10	BCL11A	chr7:63765515-63765805	GM12878	blood:	n/a	chr7:63765624-63765633
11	BCLAF1	chr7:63767445-63768047	GM12878	blood:	n/a	n/a
12	BHLHE40	chr7:63781608-63781891	GM12878	blood:	n/a	n/a
13	BHLHE40	chr7:63767644-63768132	K562	blood:	n/a	n/a
14	BHLHE40	chr7:63774140-63774632	GM12878	blood:	n/a	n/a
15	BHLHE40	chr7:63774284-63774763	K562	blood:	n/a	n/a
16	BHLHE40	chr7:63767494-63768516	GM12878	blood:	n/a	n/a
17	BHLHE40	chr7:63765474-63765767	GM12878	blood:	n/a	n/a
18	BHLHE40	chr7:63757858-63758058	GM12878	blood:	n/a	n/a
19	BRCA1	chr7:63767579-63768199	GM12878	blood:	n/a	n/a
20	BRCA1	chr7:63774166-63774655	GM12878	blood:	n/a	n/a
21	CBX3	chr7:63767621-63767998	K562	blood:	n/a	n/a
22	CCNT2	chr7:63774245-63774765	K562	blood:	n/a	n/a
23	CEBPB	chr7:63774053-63774474	MCF-7	breast:	n/a	n/a
24	CEBPB	chr7:63747104-63747516	IMR90	lung:	n/a	n/a
25	CEBPB	chr7:63752495-63752802	IMR90	lung:	n/a	n/a
26	CEBPB	chr7:63759829-63760572	A549	lung:	n/a	n/a
27	CEBPB	chr7:63775349-63775652	K562	blood:	n/a	n/a
28	CEBPB	chr7:63761085-63761633	A549	lung:	n/a	n/a
29	CEBPB	chr7:63774049-63774416	MCF-7	breast:	n/a	n/a
30	CEBPB	chr7:63774027-63774404	IMR90	lung:	n/a	n/a
31	CEBPB	chr7:63756437-63757235	HepG2	liver:	n/a	n/a
32	CEBPB	chr7:63767572-63768199	IMR90	lung:	n/a	n/a
33	CEBPB	chr7:63761037-63761769	IMR90	lung:	n/a	n/a
34	CEBPB	chr7:63760089-63760259	K562	blood:	n/a	n/a
35	CEBPB	chr7:63753627-63754217	A549	lung:	n/a	n/a
36	CEBPB	chr7:63753584-63754252	HepG2	liver:	n/a	n/a
37	CEBPB	chr7:63747101-63747481	A549	lung:	n/a	n/a
38	CEBPB	chr7:63767878-63768131	HepG2	liver:	n/a	n/a
39	CEBPB	chr7:63761005-63761742	Hela-S3	cervix:	n/a	n/a
40	CEBPB	chr7:63747144-63747518	HepG2	liver:	n/a	n/a
41	CEBPB	chr7:63765557-63765725	K562	blood:	n/a	n/a
42	CEBPB	chr7:63756885-63756970	K562	blood:	n/a	n/a
43	CEBPB	chr7:63767764-63768200	K562	blood:	n/a	n/a
44	CEBPB	chr7:63748603-63749082	IMR90	lung:	n/a	n/a
45	CEBPB	chr7:63767910-63768125	A549	lung:	n/a	n/a
46	CEBPB	chr7:63760099-63760564	IMR90	lung:	n/a	n/a
47	CEBPB	chr7:63748621-63749078	A549	lung:	n/a	n/a
48	CEBPB	chr7:63756330-63757311	A549	lung:	n/a	n/a
49	CEBPB	chr7:63761069-63761652	K562	blood:	n/a	n/a
50	CEBPB	chr7:63774028-63774404	K562	blood:	n/a	n/a

(count:1099 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:63768139-63768189	ovcar-3	ovarian:	n/a
2	chr7:63768139-63768189	ovcar-3	ovarian:	n/a
3	chr7:63774357-63774407	PFSK-1	brain:	n/a
4	chr7:63774078-63774128	HUVEC	blood vessel:	n/a
5	chr7:63767841-63767891	BE2_C	brain:	n/a
6	chr7:63766189-63766239	AG09309	skin:	n/a
7	chr7:63774078-63774128	GM06990	blood:	n/a
8	chr7:63767753-63767803	PrEC	prostate:	n/a
9	chr7:63772811-63772861	SK-N-SH_RA	brain:	n/a
10	chr7:63774357-63774407	NHBE	bronchial:	n/a
11	chr7:63771798-63771848	HCM	heart:	n/a
12	chr7:63767240-63767290	H1-hESC	embryonic stem cell:	embryo
13	chr7:63774718-63774768	MCF10A-Er-Src	breast:	n/a
14	chr7:63774078-63774128	HEEpiC	esophagus:	n/a
15	chr7:63771803-63771853	NHDF-neo	bronchial:	n/a
16	chr7:63767753-63767803	AG04449	skin:	fetal
17	chr7:63774078-63774128	HPAEpiC	pulmonary alveolar:	n/a
18	chr7:63767753-63767803	HEEpiC	esophagus:	n/a
19	chr7:63774718-63774768	HCT-116	colon:	n/a
20	chr7:63774181-63774231	MCF-7	breast:	n/a
21	chr7:63767240-63767290	HEEpiC	esophagus:	n/a
22	chr7:63774340-63774390	GM06990	blood:	n/a
23	chr7:63767240-63767290	LNCaP	prostate:	n/a
24	chr7:63774078-63774128	PANC-1	pancreas:	n/a
25	chr7:63774897-63774947	ovcar-3	ovarian:	n/a
26	chr7:63766189-63766239	SKMC	muscle:	n/a
27	chr7:63767990-63768040	IMR90	lung:	fetal
28	chr7:63774078-63774128	AG09309	skin:	n/a
29	chr7:63774357-63774407	Hela-S3	cervix:	n/a
30	chr7:63774897-63774947	LNCaP	prostate:	n/a
31	chr7:63774718-63774768	PFSK-1	brain:	n/a
32	chr7:63764120-63764170	Caco-2	colon:	n/a
33	chr7:63774357-63774407	SK-N-MC	brain:	n/a
34	chr7:63774504-63774554	HUVEC	blood vessel:	n/a
35	chr7:63767990-63768040	HEEpiC	esophagus:	n/a
36	chr7:63767240-63767290	AG09319	gingival:	n/a
37	chr7:63774718-63774768	BE2_C	brain:	n/a
38	chr7:63774181-63774231	AG09319	gingival:	n/a
39	chr7:63774181-63774231	GM12891	blood:	n/a
40	chr7:63774504-63774554	HMEC	breast:	n/a
41	chr7:63774504-63774554	IMR90	lung:	fetal
42	chr7:63771027-63771077	AG10803	skin:	n/a
43	chr7:63774357-63774407	LNCaP	prostate:	n/a
44	chr7:63772811-63772861	HCF	heart:	n/a
45	chr7:63767753-63767803	A549	lung:	n/a
46	chr7:63774340-63774390	GM19239	blood:	n/a
47	chr7:63767240-63767290	AG10803	skin:	n/a
48	chr7:63774181-63774231	BJ	skin:	n/a
49	chr7:63774078-63774128	HAEpiC	amniotic membrane:	n/a
50	chr7:63774504-63774554	NHDF-neo	bronchial:	n/a

(count:26 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:90539200..90540047-chr7:63767382..63768378,2	NB4	blood:
2	chr11:60928812..60929446-chr7:63773946..63774446,2	NB4	blood:
3	chr7:63766171..63770866-chr7:63770990..63776052,17	MCF-7	breast:
4	chr7:63774364..63776999-chr7:63780245..63782116,2	MCF-7	breast:
5	chr7:63770902..63772657-chr7:63773967..63776295,2	MCF-7	breast:
6	chr7:63766171..63770866-chr7:63770990..63776052,17	MCF-7	breast:
7	chr7:63767013..63769574-chr7:63775619..63777448,2	K562	blood:
8	chr7:26240180..26240884-chr7:63774335..63774890,2	NB4	blood:
9	chr7:63772917..63775872-chr7:64021942..64025037,3	MCF-7	breast:
10	chr7:63767348..63769333-chr7:63777033..63778934,2	MCF-7	breast:
11	chr7:63776375..63777997-chr7:63779996..63782767,2	K562	blood:
12	chr7:63770902..63772657-chr7:63773967..63776295,2	MCF-7	breast:
13	chr7:63773941..63774744-chr7:100487108..100487984,2	NB4	blood:
14	chr7:63779238..63780856-chr7:63785722..63788105,2	K562	blood:
15	chr7:63783173..63784738-chr7:63784959..63786518,2	K562	blood:
16	chr7:63776375..63777997-chr7:63779996..63782767,2	K562	blood:
17	chr7:63774618..63777610-chr7:63777696..63779466,2	K562	blood:
18	chr7:63765720..63769257-chr7:63771192..63774527,5	K562	blood:
19	chr7:63766445..63770083-chr7:63772313..63776161,6	MCF-7	breast:
20	chr7:63766214..63769574-chr7:63772661..63777448,6	K562	blood:
21	chr7:63671704..63673341-chr7:63777924..63780432,2	K562	blood:
22	chr7:63765720..63769257-chr7:63771192..63774527,5	K562	blood:
23	chr7:63779207..63780856-chr7:63784843..63787222,2	K562	blood:
24	chr7:63774618..63777610-chr7:63777696..63779466,2	K562	blood:
25	chr7:63766445..63770083-chr7:63772313..63776161,6	MCF-7	breast:
26	chr7:63766214..63769574-chr7:63772661..63777448,6	K562	blood:

(count:21 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZNF736-3	chr7:63774251-63774395	NONHSAT120996
2	lnc-ZNF736-3	chr7:63768839-63769003	NONHSAT120999
3	lnc-ZNF736-3	chr7:63767916-63768246	NONHSAT120999
4	lnc-ZNF680-16	chr7:63748767-63748921	NONHSAT120989
5	lnc-ZNF736-3	chr7:63768839-63769003	NONHSAT120996
6	lnc-ZNF679-1	chr7:63782148-63784698	ucscGeneNc_uc003ttf_2
7	lnc-ZNF679-1	chr7:63781900-63782018	ucscGeneNc_uc003ttf_2
8	lnc-ZNF736-3	chr7:63768359-63768693	NONHSAT120999
9	lnc-ZNF680-16	chr7:63749814-63749869	NONHSAT120989
10	lnc-ZNF680-15	chr7:63759918-63759938	NONHSAT120990
11	lnc-ZNF680-1	chr7:63761528-63761562	XLOC_006471
12	lnc-ZNF736-3	chr7:63773186-63773229	NONHSAT120996
13	lnc-ZNF736-3	chr7:63768535-63768693	NONHSAT121000
14	lnc-ZNF736-3	chr7:63768359-63771357	NONHSAT120995
15	lnc-ZNF736-3	chr7:63768839-63769169	NONHSAT121000
16	lnc-ZNF680-15	chr7:63754887-63755097	NONHSAT120990
17	lnc-ZNF736-3	chr7:63767821-63768060	NONHSAT120995
18	lnc-ZNF736-3	chr7:63767837-63768060	NONHSAT120996
19	lnc-ZNF679-1	chr7:63778946-63779035	ucscGeneNc_uc003ttf_2
20	lnc-ZNF736-3	chr7:63770656-63770716	NONHSAT120999
21	lnc-ZNF680-1	chr7:63762711-63763122	XLOC_006471

No data

Variant related genes	Relation type
ZNF736	TF binding region
ZNF736	CpG island
ENSG00000118412	chromatin interactions
ENSG00000122566	chromatin interactions
ENSG00000167987	chromatin interactions
ENSG00000173041	chromatin interactions
ENSG00000234444	chromatin interactions
ENSG00000122565	chromatin interactions
ENSG00000176125	chromatin interactions

Extended variants
information (count: 886 )
Associated
traits (count: 77 )

Variant overlapped rSNPs/rCNVs (count:886 , 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	rs117039264	chr7:63748774-63748775	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
2	rs566162077	chr7:63748789-63748790	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
3	rs376280065	chr7:63748800-63748801	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
4	rs10949886	chr7:63748827-63748828	Inactive region	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs570478612	chr7:63748836-63748837	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
6	rs556466942	chr7:63748893-63748894	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
7	rs144717308	chr7:63748902-63748903	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
8	rs115201159	chr7:63749821-63749822	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
9	rs117997520	chr7:63749830-63749831	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
10	rs542996693	chr7:63749862-63749863	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
11	rs535135116	chr7:63754909-63754910	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
12	rs181598886	chr7:63754928-63754929	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
13	rs202008142	chr7:63754937-63754938	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
14	rs369258129	chr7:63755080-63755081	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
15	rs576039385	chr7:63755095-63755096	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
16	rs539329989	chr7:63759822-63759823	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs369085977	chr7:63759827-63759828	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs576128191	chr7:63759848-63759849	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs373047655	chr7:63759871-63759872	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs182956065	chr7:63759991-63759992	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs536185776	chr7:63760020-63760021	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs541477755	chr7:63760049-63760050	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs558170130	chr7:63760072-63760073	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs73700526	chr7:63760082-63760083	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs188233578	chr7:63760181-63760182	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs113304548	chr7:63760182-63760183	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs34421808	chr7:63760187-63760188	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs529429464	chr7:63760189-63760190	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs191463768	chr7:63760190-63760191	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs561490312	chr7:63760224-63760225	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs527373867	chr7:63760260-63760261	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs554684080	chr7:63760268-63760269	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs628142	chr7:63760276-63760277	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs374204217	chr7:63760287-63760288	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs144498921	chr7:63760300-63760301	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs148547416	chr7:63760357-63760358	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs142933790	chr7:63760378-63760379	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs182790720	chr7:63760577-63760578	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs370253081	chr7:63760601-63760602	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs535337684	chr7:63760614-63760615	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs146285913	chr7:63760623-63760624	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs551271572	chr7:63760637-63760638	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs566213881	chr7:63760668-63760669	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs10239178	chr7:63760706-63760707	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs630324	chr7:63760720-63760721	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs151112832	chr7:63760732-63760733	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs544107970	chr7:63760743-63760744	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs77850246	chr7:63760753-63760754	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs79866126	chr7:63760773-63760774	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs79879617	chr7:63760794-63760795	Enhancers	n/a	n/a	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
Non-syndromic sensorineural hearing loss	21293372	CNVD
Glioblastoma multiforme	21390271	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:967 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:63759800-63762200	Enhancers	Placenta	Placenta
2	chr7:63762200-63766600	Weak transcription	Placenta	Placenta
3	chr7:63764600-63767000	Enhancers	Primary monocytes fromperipheralblood	blood
4	chr7:63764800-63766600	Enhancers	Monocytes-CD14+_RO01746	blood
5	chr7:63764800-63767000	Enhancers	Primary B cells from peripheral blood	blood
6	chr7:63765000-63765400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
7	chr7:63765000-63765600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
8	chr7:63765000-63766800	Enhancers	Primary B cells from cord blood	blood
9	chr7:63765000-63766800	Enhancers	GM12878-XiMat	blood
10	chr7:63765200-63765400	Enhancers	Colonic Mucosa	Colon
11	chr7:63765400-63766600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
12	chr7:63765400-63766600	Weak transcription	Colonic Mucosa	Colon
13	chr7:63765600-63766000	Enhancers	Primary hematopoietic stem cells short term culture	blood
14	chr7:63765600-63766000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
15	chr7:63765800-63766200	Enhancers	Primary hematopoietic stem cells	blood
16	chr7:63766000-63766200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
17	chr7:63766000-63766600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
18	chr7:63766200-63766400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
19	chr7:63766200-63766400	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
20	chr7:63766200-63766400	Enhancers	Fetal Lung	lung
21	chr7:63766200-63766600	Weak transcription	Primary hematopoietic stem cells	blood
22	chr7:63766200-63766600	Active TSS	Skeletal Muscle Male	skeletal muscle
23	chr7:63766200-63766800	Active TSS	Primary hematopoietic stem cells short term culture	blood
24	chr7:63766200-63766800	Enhancers	Skeletal Muscle Female	skeletal muscle
25	chr7:63766400-63766600	Enhancers	Breast Myoepithelial Primary Cells	Breast
26	chr7:63766400-63766600	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
27	chr7:63766400-63766600	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
28	chr7:63766400-63766600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
29	chr7:63766400-63766600	Enhancers	Adipose Nuclei	Adipose
30	chr7:63766400-63766600	Enhancers	Aorta	Aorta
31	chr7:63766400-63766600	Enhancers	Brain Angular Gyrus	brain
32	chr7:63766400-63766600	Enhancers	Brain Hippocampus Middle	brain
33	chr7:63766400-63766600	Enhancers	Brain Inferior Temporal Lobe	brain
34	chr7:63766400-63766600	Enhancers	Rectal Mucosa Donor 29	rectum
35	chr7:63766400-63766600	Enhancers	Rectal Smooth Muscle	rectum
36	chr7:63766400-63766600	Enhancers	Dnd41	blood
37	chr7:63766400-63766800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
38	chr7:63766400-63766800	Enhancers	Primary T cells fromperipheralblood	blood
39	chr7:63766400-63766800	Enhancers	Primary T killer memory cells from peripheral blood	blood
40	chr7:63766400-63766800	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
41	chr7:63766400-63766800	Enhancers	Cortex derived primary cultured neurospheres	brain
42	chr7:63766400-63766800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
43	chr7:63766400-63766800	Enhancers	Brain Cingulate Gyrus	brain
44	chr7:63766400-63766800	Enhancers	Fetal Kidney	kidney
45	chr7:63766400-63766800	Enhancers	Fetal Muscle Leg	muscle
46	chr7:63766400-63767000	Flanking Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
47	chr7:63766400-63767000	Flanking Active TSS	Fetal Lung	lung
48	chr7:63766400-63767600	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
49	chr7:63766400-63768000	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
50	chr7:63766400-63768000	Active TSS	Stomach Smooth Muscle	stomach

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