Variant report

Variant	nsv1024790
Chromosome Location	chr7:63694330-63766444
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:193)
CpG islands
(count:305)
Chromatin interactive
region (count:3)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:193 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr7:63765452-63765906	GM12878	blood:	n/a	n/a
2	BATF	chr7:63738009-63738322	GM12878	blood:	n/a	n/a
3	BATF	chr7:63738084-63738326	GM12878	blood:	n/a	n/a
4	BATF	chr7:63757823-63758057	GM12878	blood:	n/a	chr7:63757944-63757955
5	BATF	chr7:63757784-63758164	GM12878	blood:	n/a	chr7:63757944-63757955
6	BCL11A	chr7:63765515-63765805	GM12878	blood:	n/a	chr7:63765624-63765633
7	BCL11A	chr7:63765504-63765813	GM12878	blood:	n/a	chr7:63765624-63765633
8	BHLHE40	chr7:63757858-63758058	GM12878	blood:	n/a	n/a
9	BHLHE40	chr7:63738003-63738410	GM12878	blood:	n/a	n/a
10	BHLHE40	chr7:63765474-63765767	GM12878	blood:	n/a	n/a
11	BHLHE40	chr7:63702502-63702691	A549	lung:	n/a	n/a
12	CEBPB	chr7:63752711-63752717	K562	blood:	n/a	n/a
13	CEBPB	chr7:63748603-63749082	IMR90	lung:	n/a	n/a
14	CEBPB	chr7:63760119-63760583	HepG2	liver:	n/a	n/a
15	CEBPB	chr7:63743535-63743813	HepG2	liver:	n/a	n/a
16	CEBPB	chr7:63701582-63702144	IMR90	lung:	n/a	n/a
17	CEBPB	chr7:63761068-63761729	MCF-7	breast:	n/a	n/a
18	CEBPB	chr7:63756437-63757235	HepG2	liver:	n/a	n/a
19	CEBPB	chr7:63761036-63761470	MCF-7	breast:	n/a	n/a
20	CEBPB	chr7:63750583-63750784	HepG2	liver:	n/a	n/a
21	CEBPB	chr7:63700010-63700383	A549	lung:	n/a	chr7:63700187-63700198
22	CEBPB	chr7:63761067-63761760	HepG2	liver:	n/a	n/a
23	CEBPB	chr7:63760099-63760564	IMR90	lung:	n/a	n/a
24	CEBPB	chr7:63756885-63756970	K562	blood:	n/a	n/a
25	CEBPB	chr7:63747101-63747481	A549	lung:	n/a	n/a
26	CEBPB	chr7:63753627-63754217	A549	lung:	n/a	n/a
27	CEBPB	chr7:63700707-63700753	A549	lung:	n/a	n/a
28	CEBPB	chr7:63745056-63745702	HepG2	liver:	n/a	n/a
29	CEBPB	chr7:63747144-63747518	HepG2	liver:	n/a	n/a
30	CEBPB	chr7:63753584-63754252	HepG2	liver:	n/a	n/a
31	CEBPB	chr7:63700006-63700357	HepG2	liver:	n/a	chr7:63700187-63700198
32	CEBPB	chr7:63761037-63761769	IMR90	lung:	n/a	n/a
33	CEBPB	chr7:63752481-63752792	HepG2	liver:	n/a	n/a
34	CEBPB	chr7:63748621-63749078	A549	lung:	n/a	n/a
35	CEBPB	chr7:63752495-63752802	IMR90	lung:	n/a	n/a
36	CEBPB	chr7:63756330-63757311	A549	lung:	n/a	n/a
37	CEBPB	chr7:63759829-63760572	A549	lung:	n/a	n/a
38	CEBPB	chr7:63703922-63704229	A549	lung:	n/a	n/a
39	CEBPB	chr7:63760089-63760259	K562	blood:	n/a	n/a
40	CEBPB	chr7:63701878-63701962	K562	blood:	n/a	n/a
41	CEBPB	chr7:63703755-63704081	HepG2	liver:	n/a	n/a
42	CEBPB	chr7:63701539-63701771	MCF-7	breast:	n/a	n/a
43	CEBPB	chr7:63701509-63702061	Hela-S3	cervix:	n/a	n/a
44	CEBPB	chr7:63761085-63761633	A549	lung:	n/a	n/a
45	CEBPB	chr7:63761069-63761652	K562	blood:	n/a	n/a
46	CEBPB	chr7:63747104-63747516	IMR90	lung:	n/a	n/a
47	CEBPB	chr7:63765557-63765725	K562	blood:	n/a	n/a
48	CEBPB	chr7:63701627-63702117	HepG2	liver:	n/a	n/a
49	CEBPB	chr7:63761005-63761742	Hela-S3	cervix:	n/a	n/a
50	CEBPB	chr7:63748634-63749186	HepG2	liver:	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	chr7:63709487-63709537	AG09319	gingival:	n/a
2	chr7:63709487-63709537	HCM	heart:	n/a
3	chr7:63764120-63764170	AG04449	skin:	fetal
4	chr7:63709633-63709683	HRCEpiC	kidney:	n/a
5	chr7:63709487-63709537	LNCaP	prostate:	n/a
6	chr7:63709633-63709683	Hepatocyte	liver:	n/a
7	chr7:63709487-63709537	HepG2	liver:	n/a
8	chr7:63741486-63741536	A549	lung:	n/a
9	chr7:63764120-63764170	NH-A	brain:	n/a
10	chr7:63709633-63709683	AG04450	lung:	fetal
11	chr7:63709487-63709537	SKMC	muscle:	n/a
12	chr7:63709487-63709537	AoSMC	blood vessel:	n/a
13	chr7:63766189-63766239	SK-N-SH_RA	brain:	n/a
14	chr7:63766189-63766239	HCPEpiC	choroid plexus:	n/a
15	chr7:63709487-63709537	CMK	blood:	n/a
16	chr7:63741486-63741536	H1-hESC	embryonic stem cell:	embryo
17	chr7:63741486-63741536	PANC-1	pancreas:	n/a
18	chr7:63741486-63741536	GM19239	blood:	n/a
19	chr7:63709487-63709537	HEK293	kidney:	embryo
20	chr7:63709633-63709683	HL-60	blood:	n/a
21	chr7:63741486-63741536	HCT-116	colon:	n/a
22	chr7:63766189-63766239	NHDF-neo	bronchial:	n/a
23	chr7:63709633-63709683	NH-A	brain:	n/a
24	chr7:63764120-63764170	HNPCEpiC	eye:	n/a
25	chr7:63709633-63709683	BJ	skin:	n/a
26	chr7:63766189-63766239	H1-hESC	embryonic stem cell:	embryo
27	chr7:63764120-63764170	BE2_C	brain:	n/a
28	chr7:63764120-63764170	Jurkat	blood:	n/a
29	chr7:63709633-63709683	AoSMC	blood vessel:	n/a
30	chr7:63741486-63741536	NHBE	bronchial:	n/a
31	chr7:63741486-63741536	HCM	heart:	n/a
32	chr7:63709487-63709537	HRPEpiC	eye:	n/a
33	chr7:63741486-63741536	AG04450	lung:	fetal
34	chr7:63709633-63709683	LNCaP	prostate:	n/a
35	chr7:63741486-63741536	HAEpiC	amniotic membrane:	n/a
36	chr7:63741486-63741536	HEK293	kidney:	embryo
37	chr7:63709487-63709537	H1-hESC	embryonic stem cell:	embryo
38	chr7:63709633-63709683	SKMC	muscle:	n/a
39	chr7:63741486-63741536	HUVEC	blood vessel:	n/a
40	chr7:63764120-63764170	AG09309	skin:	n/a
41	chr7:63764120-63764170	NHDF-neo	bronchial:	n/a
42	chr7:63709633-63709683	PFSK-1	brain:	n/a
43	chr7:63709633-63709683	HCPEpiC	choroid plexus:	n/a
44	chr7:63766189-63766239	HCT-116	colon:	n/a
45	chr7:63741486-63741536	Caco-2	colon:	n/a
46	chr7:63764120-63764170	Hela-S3	cervix:	n/a
47	chr7:63764120-63764170	NHBE	bronchial:	n/a
48	chr7:63741486-63741536	HPAEpiC	pulmonary alveolar:	n/a
49	chr7:63764120-63764170	AG10803	skin:	n/a
50	chr7:63709487-63709537	SK-N-SH	brain:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr7:63765720..63769257-chr7:63771192..63774527,5	K562	blood:
2	chr7:63766214..63769574-chr7:63772661..63777448,6	K562	blood:
3	chr7:63766171..63770866-chr7:63770990..63776052,17	MCF-7	breast:

(count:6 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZNF680-16	chr7:63749814-63749869	NONHSAT120989
2	lnc-ZNF680-15	chr7:63754887-63755097	NONHSAT120990
3	lnc-ZNF680-16	chr7:63748767-63748921	NONHSAT120989
4	lnc-ZNF680-15	chr7:63759918-63759938	NONHSAT120990
5	lnc-ZNF680-1	chr7:63762711-63763122	XLOC_006471
6	lnc-ZNF680-1	chr7:63761528-63761562	XLOC_006471

No data

Variant related genes	Relation type
ZNF736	TF binding region
ZNF679	TF binding region
ZNF736	CpG island
ZNF679	CpG island
ENSG00000234444	chromatin interactions

Extended variants
information (count: 500 )
Associated
traits (count: 78 )

Variant overlapped rSNPs/rCNVs (count:500 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs557773465	chr7:63694354-63694355	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
2	rs559745263	chr7:63694363-63694364	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
3	rs528666686	chr7:63694368-63694369	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
4	rs571264729	chr7:63694372-63694373	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
5	rs77758591	chr7:63694386-63694387	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
6	rs569032288	chr7:63708664-63708665	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs13244780	chr7:63708687-63708688	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs546167937	chr7:63708700-63708701	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs556501848	chr7:63708711-63708712	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs535620208	chr7:63709315-63709316	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs75059739	chr7:63709325-63709326	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs546628495	chr7:63709326-63709327	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs182240624	chr7:63709362-63709363	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs374951221	chr7:63709423-63709424	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs368170297	chr7:63709430-63709431	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs541171498	chr7:63709445-63709446	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs564242090	chr7:63709446-63709447	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs186800690	chr7:63709449-63709450	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs144272859	chr7:63709467-63709468	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs563979238	chr7:63709482-63709483	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs117470203	chr7:63709487-63709488	Inactive region	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
22	rs75120535	chr7:63715612-63715613	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
23	rs144344125	chr7:63715678-63715679	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
24	rs564652037	chr7:63715689-63715690	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
25	rs541909745	chr7:63715781-63715782	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
26	rs571577894	chr7:63723650-63723651	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
27	rs542145925	chr7:63723706-63723707	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
28	rs561815922	chr7:63723726-63723727	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
29	rs537068376	chr7:63723731-63723732	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
30	rs557664787	chr7:63723760-63723761	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
31	rs113419366	chr7:63723766-63723767	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
32	rs571008875	chr7:63725600-63725601	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs35638959	chr7:63725626-63725627	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs556647629	chr7:63725762-63725763	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs184164154	chr7:63725770-63725771	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs140984708	chr7:63725884-63725885	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
37	rs188518613	chr7:63725887-63725888	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
38	rs146475309	chr7:63726017-63726018	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
39	rs573094210	chr7:63726058-63726059	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
40	rs545184779	chr7:63726149-63726150	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
41	rs76466159	chr7:63726151-63726152	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
42	rs150208297	chr7:63726166-63726167	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
43	rs180977342	chr7:63726179-63726180	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
44	rs561387175	chr7:63726184-63726185	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
45	rs185006343	chr7:63726204-63726205	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
46	rs546714170	chr7:63726208-63726209	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
47	rs560832580	chr7:63726221-63726222	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
48	rs10262403	chr7:63726230-63726231	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs552841085	chr7:63726276-63726277	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
50	rs569069333	chr7:63726286-63726287	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:78)

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
Pancreatic cancer	17952125	CNVD
Glioblastoma multiforme	21390271	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:63 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:63693600-63694400	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
2	chr7:63715600-63715800	ZNF genes & repeats	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr7:63723600-63723800	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr7:63725600-63725800	Weak transcription	NHDF-Ad	bronchial
5	chr7:63725800-63728600	ZNF genes & repeats	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
6	chr7:63726200-63726400	ZNF genes & repeats	NHDF-Ad	bronchial
7	chr7:63731800-63732200	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
8	chr7:63738000-63738400	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
9	chr7:63742600-63743000	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
10	chr7:63759800-63762200	Enhancers	Placenta	Placenta
11	chr7:63762200-63766600	Weak transcription	Placenta	Placenta
12	chr7:63764600-63767000	Enhancers	Primary monocytes fromperipheralblood	blood
13	chr7:63764800-63766600	Enhancers	Monocytes-CD14+_RO01746	blood
14	chr7:63764800-63767000	Enhancers	Primary B cells from peripheral blood	blood
15	chr7:63765000-63765400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
16	chr7:63765000-63765600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
17	chr7:63765000-63766800	Enhancers	Primary B cells from cord blood	blood
18	chr7:63765000-63766800	Enhancers	GM12878-XiMat	blood
19	chr7:63765200-63765400	Enhancers	Colonic Mucosa	Colon
20	chr7:63765400-63766600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
21	chr7:63765400-63766600	Weak transcription	Colonic Mucosa	Colon
22	chr7:63765600-63766000	Enhancers	Primary hematopoietic stem cells short term culture	blood
23	chr7:63765600-63766000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
24	chr7:63765800-63766200	Enhancers	Primary hematopoietic stem cells	blood
25	chr7:63766000-63766200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
26	chr7:63766000-63766600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
27	chr7:63766200-63766400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
28	chr7:63766200-63766400	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
29	chr7:63766200-63766400	Enhancers	Fetal Lung	lung
30	chr7:63766200-63766600	Weak transcription	Primary hematopoietic stem cells	blood
31	chr7:63766200-63766600	Active TSS	Skeletal Muscle Male	skeletal muscle
32	chr7:63766200-63766800	Active TSS	Primary hematopoietic stem cells short term culture	blood
33	chr7:63766200-63766800	Enhancers	Skeletal Muscle Female	skeletal muscle
34	chr7:63766400-63766600	Enhancers	Breast Myoepithelial Primary Cells	Breast
35	chr7:63766400-63766600	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
36	chr7:63766400-63766600	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
37	chr7:63766400-63766600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
38	chr7:63766400-63766600	Enhancers	Adipose Nuclei	Adipose
39	chr7:63766400-63766600	Enhancers	Aorta	Aorta
40	chr7:63766400-63766600	Enhancers	Brain Angular Gyrus	brain
41	chr7:63766400-63766600	Enhancers	Brain Hippocampus Middle	brain
42	chr7:63766400-63766600	Enhancers	Brain Inferior Temporal Lobe	brain
43	chr7:63766400-63766600	Enhancers	Rectal Mucosa Donor 29	rectum
44	chr7:63766400-63766600	Enhancers	Rectal Smooth Muscle	rectum
45	chr7:63766400-63766600	Enhancers	Dnd41	blood
46	chr7:63766400-63766800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
47	chr7:63766400-63766800	Enhancers	Primary T cells fromperipheralblood	blood
48	chr7:63766400-63766800	Enhancers	Primary T killer memory cells from peripheral blood	blood
49	chr7:63766400-63766800	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
50	chr7:63766400-63766800	Enhancers	Cortex derived primary cultured neurospheres	brain

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