Variant report

Variant	nsv1033898
Chromosome Location	chr7:146721499-147081768
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:809)
CpG islands
(count:306)
Chromatin interactive
region (count:35)
LncRNA
region (count:6)
Mature miRNA
region (count: 1)
miRNA target
sites (count:0)

(count:809 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:146942453-146942657	K562	blood:	n/a	n/a
2	ARID3A	chr7:146873275-146873410	K562	blood:	n/a	n/a
3	ARID3A	chr7:146855481-146855483	K562	blood:	n/a	n/a
4	ATF2	chr7:146850658-146851014	GM12878	blood:	n/a	n/a
5	ATF2	chr7:146850699-146851048	GM12878	blood:	n/a	n/a
6	BACH1	chr7:146858480-146858869	H1-hESC	embryonic stem cell:	n/a	chr7:146858693-146858707
7	BACH1	chr7:146842403-146842603	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr7:146796893-146796911	K562	blood:	n/a	n/a
9	BATF	chr7:146793808-146794055	GM12878	blood:	n/a	n/a
10	BHLHE40	chr7:146850941-146850943	GM12878	blood:	n/a	n/a
11	CEBPB	chr7:146983597-146983710	HepG2	liver:	n/a	chr7:146983658-146983669 chr7:146983636-146983653 chr7:146983657-146983668
12	CEBPB	chr7:146769619-146769984	HepG2	liver:	n/a	chr7:146769802-146769813 chr7:146769801-146769812
13	CEBPB	chr7:146769642-146769941	A549	lung:	n/a	chr7:146769802-146769813 chr7:146769801-146769812
14	CEBPB	chr7:146738575-146738797	HepG2	liver:	n/a	chr7:146738715-146738732 chr7:146738754-146738767
15	CEBPB	chr7:146976578-146977316	HepG2	liver:	n/a	n/a
16	CEBPB	chr7:146846869-146846957	HepG2	liver:	n/a	chr7:146846897-146846908
17	CEBPB	chr7:146846864-146846986	A549	lung:	n/a	chr7:146846897-146846908
18	CEBPB	chr7:146794034-146794272	A549	lung:	n/a	chr7:146794140-146794153 chr7:146794140-146794151
19	CEBPB	chr7:146793958-146794294	HepG2	liver:	n/a	chr7:146794140-146794153 chr7:146794140-146794151
20	CEBPB	chr7:146769719-146769861	H1-hESC	embryonic stem cell:	n/a	chr7:146769802-146769813 chr7:146769801-146769812
21	CEBPB	chr7:146842223-146842579	H1-hESC	embryonic stem cell:	n/a	n/a
22	CEBPB	chr7:146830735-146831054	HepG2	liver:	n/a	chr7:146830912-146830923 chr7:146830910-146830927
23	CEBPB	chr7:146832319-146832519	HepG2	liver:	n/a	n/a
24	CEBPB	chr7:146890827-146890833	H1-hESC	embryonic stem cell:	n/a	n/a
25	CEBPB	chr7:146769663-146769977	K562	blood:	n/a	chr7:146769802-146769813 chr7:146769801-146769812
26	CEBPB	chr7:146843108-146843141	K562	blood:	n/a	chr7:146843117-146843130 chr7:146843117-146843128
27	CEBPB	chr7:146947772-146947947	HepG2	liver:	n/a	chr7:146947806-146947817
28	CEBPB	chr7:146769642-146769942	IMR90	lung:	n/a	chr7:146769802-146769813 chr7:146769801-146769812
29	CEBPB	chr7:146846845-146846953	K562	blood:	n/a	chr7:146846897-146846908
30	CEBPB	chr7:146942460-146942723	H1-hESC	embryonic stem cell:	n/a	n/a
31	CEBPZ	chr7:146762179-146762302	HepG2	liver:	n/a	n/a
32	CHD2	chr7:146942436-146942788	H1-hESC	embryonic stem cell:	n/a	n/a
33	CTBP2	chr7:146842373-146842945	H1-hESC	embryonic stem cell:	n/a	n/a
34	CTCF	chr7:146942500-146942650	HEK293	kidney:	n/a	n/a
35	CTCF	chr7:146942401-146942708	T-47D	breast:	n/a	n/a
36	CTCF	chr7:146947180-146947330	HAc	cerebellar:	n/a	n/a
37	CTCF	chr7:146942371-146942715	K562	blood:	n/a	n/a
38	CTCF	chr7:146942460-146942610	MCF-7	breast:	n/a	n/a
39	CTCF	chr7:146942412-146942718	MCF-7	breast:	n/a	n/a
40	CTCF	chr7:146942480-146942630	HepG2	liver:	n/a	n/a
41	CTCF	chr7:146733716-146733792	GM20000	blood:	n/a	n/a
42	CTCF	chr7:146942480-146942630	HA-sp	spinal cord:	n/a	n/a
43	CTCF	chr7:146942460-146942610	GM06990	blood:	n/a	n/a
44	CTCF	chr7:146942440-146942590	GM12865	blood:	n/a	n/a
45	CTCF	chr7:146947160-146947310	Caco-2	colon:	n/a	n/a
46	CTCF	chr7:146942455-146942684	GM10266	blood:	n/a	n/a
47	CTCF	chr7:146942468-146942667	Hela-S3	cervix:	n/a	n/a
48	CTCF	chr7:146733960-146734110	HPAF	blood vessel:	n/a	n/a
49	CTCF	chr7:146954920-146955070	AG09319	gingival:	n/a	n/a
50	CTCF	chr7:146942371-146942836	MCF-7	breast:	n/a	n/a

(count:306 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:146904205-146904255	CMK	blood:	n/a
2	chr7:146904205-146904255	CMK	blood:	n/a
3	chr7:147065665-147065715	BJ	skin:	n/a
4	chr7:147065665-147065715	AoSMC	blood vessel:	n/a
5	chr7:146842348-146842398	HAEpiC	amniotic membrane:	n/a
6	chr7:146820536-146820586	Hepatocyte	liver:	n/a
7	chr7:146897691-146897741	HepG2	liver:	n/a
8	chr7:146897691-146897741	HRCEpiC	kidney:	n/a
9	chr7:146842348-146842398	HCM	heart:	n/a
10	chr7:146820536-146820586	AG09319	gingival:	n/a
11	chr7:146897691-146897741	HRPEpiC	eye:	n/a
12	chr7:146820536-146820586	NT2-D1	testis:	n/a
13	chr7:146842348-146842398	SK-N-SH	brain:	n/a
14	chr7:146820536-146820586	GM12891	blood:	n/a
15	chr7:146897691-146897741	GM12892	blood:	n/a
16	chr7:146904205-146904255	HCF	heart:	n/a
17	chr7:146904205-146904255	SK-N-SH_RA	brain:	n/a
18	chr7:146820536-146820586	T-47D	breast:	n/a
19	chr7:147065665-147065715	HAEpiC	amniotic membrane:	n/a
20	chr7:146904205-146904255	HepG2	liver:	n/a
21	chr7:146904205-146904255	NHBE	bronchial:	n/a
22	chr7:146820536-146820586	SAEC	small airway:	n/a
23	chr7:146820536-146820586	U87	brain:	n/a
24	chr7:146820536-146820586	HRPEpiC	eye:	n/a
25	chr7:146842348-146842398	Jurkat	blood:	n/a
26	chr7:147065665-147065715	CMK	blood:	n/a
27	chr7:147065665-147065715	SK-N-MC	brain:	n/a
28	chr7:146820536-146820586	HNPCEpiC	eye:	n/a
29	chr7:147065665-147065715	U87	brain:	n/a
30	chr7:146820536-146820586	NHBE	bronchial:	n/a
31	chr7:146897691-146897741	IMR90	lung:	fetal
32	chr7:146897691-146897741	NHBE	bronchial:	n/a
33	chr7:146897691-146897741	HCPEpiC	choroid plexus:	n/a
34	chr7:146897691-146897741	AG09319	gingival:	n/a
35	chr7:146842348-146842398	ProgFib	skin:	n/a
36	chr7:146820536-146820586	K562	blood:	n/a
37	chr7:146897691-146897741	HCT-116	colon:	n/a
38	chr7:146820536-146820586	BJ	skin:	n/a
39	chr7:147065665-147065715	HUVEC	blood vessel:	n/a
40	chr7:146904205-146904255	HRCEpiC	kidney:	n/a
41	chr7:146842348-146842398	HCT-116	colon:	n/a
42	chr7:146897691-146897741	HEEpiC	esophagus:	n/a
43	chr7:146820536-146820586	GM12892	blood:	n/a
44	chr7:146897691-146897741	CMK	blood:	n/a
45	chr7:146897691-146897741	RPTEC	kidney:	n/a
46	chr7:146842348-146842398	Hepatocyte	liver:	n/a
47	chr7:146904205-146904255	SKMC	muscle:	n/a
48	chr7:146904205-146904255	NT2-D1	testis:	n/a
49	chr7:146842348-146842398	ovcar-3	ovarian:	n/a
50	chr7:147065665-147065715	NT2-D1	testis:	n/a

(count:35 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:146913926..146916451-chr7:146918952..146920556,2	K562	blood:
2	chr7:146920592..146922587-chr7:146928456..146931427,2	K562	blood:
3	chr7:146814469..146816823-chr7:146819196..146821242,2	K562	blood:
4	chr7:147018041..147019987-chr7:147042337..147044392,2	K562	blood:
5	chr7:146761282..146763181-chr7:146763573..146765951,2	K562	blood:
6	chr7:146945142..146947426-chr7:146947550..146950265,2	K562	blood:
7	chr7:146864798..146866603-chr7:146876111..146877910,2	K562	blood:
8	chr7:146947046..146947712-chr7:147780872..147781389,2	MCF-7	breast:
9	chr7:146826412..146830203-chr7:146830446..146834436,3	K562	blood:
10	chr7:146993664..146995748-chr7:147006294..147008294,2	MCF-7	breast:
11	chr7:147063148..147065759-chr7:147077085..147079029,2	K562	blood:
12	chr7:146728137..146729642-chr7:146730753..146732443,2	K562	blood:
13	chr1:83035755..83036717-chr7:147026373..147027195,2	MCF-7	breast:
14	chr7:146433613..146434480-chr7:146942002..146942841,3	MCF-7	breast:
15	chr7:146942052..146943007-chr7:147780653..147781865,8	MCF-7	breast:
16	chr7:147063148..147065759-chr7:147077085..147079029,2	K562	blood:
17	chr7:147018041..147019987-chr7:147042337..147044392,2	K562	blood:
18	chr7:146761282..146763181-chr7:146763573..146765951,2	K562	blood:
19	chr7:146715781..146717659-chr7:146720196..146724156,3	K562	blood:
20	chr7:146945142..146947426-chr7:146947550..146950265,2	K562	blood:
21	chr7:146993664..146995748-chr7:147006294..147008294,2	MCF-7	breast:
22	chr7:147045457..147047946-chr7:147059907..147061995,2	K562	blood:
23	chr7:146913926..146916451-chr7:146918952..146920556,2	K562	blood:
24	chr7:146728137..146729642-chr7:146730753..146732443,2	K562	blood:
25	chr7:147065836..147067829-chr7:147068950..147071013,2	MCF-7	breast:
26	chr7:146989620..146992429-chr7:146994596..146997108,3	K562	blood:
27	chr7:146771218..146771738-chrX:153626554..153627086,2	Hela-S3	cervix:
28	chr7:146814469..146816823-chr7:146819196..146821242,2	K562	blood:
29	chr7:146989620..146992429-chr7:146994596..146997108,3	K562	blood:
30	chr7:147065836..147067829-chr7:147068950..147071013,2	MCF-7	breast:
31	chr7:146864798..146866603-chr7:146876111..146877910,2	K562	blood:
32	chr7:146920592..146922587-chr7:146928456..146931427,2	K562	blood:
33	chr7:146826412..146830203-chr7:146830446..146834436,3	K562	blood:
34	chr7:146963308..146964971-chr7:147095158..147097762,2	MCF-7	breast:
35	chr7:147045457..147047946-chr7:147059907..147061995,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-EZH2-4	chr7:146782785-146782914	ENSG00000236795.1
2	lnc-C7orf33-8	chr7:146843434-146843848	NONHSAT123953
3	lnc-EZH2-4	chr7:146794524-146794701	ENSG00000236795.1
4	lnc-C7orf33-7	chr7:146864436-146864664	NONHSAT123954
5	lnc-EZH2-4	chr7:146778026-146779180	ENSG00000236795.1
6	lnc-EZH2-4	chr7:146779632-146780313	ENSG00000236795.1

miRNA name	Chromosome Location	mirBase accession
hsa-miR-548f-3p	chr7:147075133-147075151	MIMAT0005895_3

No data

Variant related genes	Relation type
ENSG00000236795	TF binding region
RANP2	TF binding region
DUTP3	TF binding region
MIR548F4	TF binding region
ENSG00000236795	CpG island
RANP2	CpG island
DUTP3	CpG island
MIR548F4	CpG island
ENSG00000147403	chromatin interactions

Extended variants
information (count: 4996 )
Associated
traits (count: 99 )

Variant overlapped rSNPs/rCNVs (count:4996 , 50 per page) page: 1 2 3 4 5 6 7 ... 100

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs555632122	chr7:146722202-146722203	Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs62483991	chr7:146722234-146722235	Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs78889580	chr7:146722235-146722236	Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs373026647	chr7:146722269-146722270	Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs148445086	chr7:146722281-146722282	Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs62483992	chr7:146722285-146722286	Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs146568654	chr7:146722292-146722293	Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs563739467	chr7:146722293-146722294	Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs529483384	chr7:146722309-146722310	Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs62483993	chr7:146722317-146722318	Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs189806992	chr7:146722434-146722435	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs559977546	chr7:146722464-146722465	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs376711752	chr7:146722598-146722599	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs75783419	chr7:146730805-146730806	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs192136779	chr7:146730833-146730834	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs12672922	chr7:146730834-146730835	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs559629701	chr7:146730840-146730841	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs573073984	chr7:146730891-146730892	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs74969810	chr7:146730904-146730905	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs530913382	chr7:146730914-146730915	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs75390289	chr7:146730918-146730919	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs565021120	chr7:146730941-146730942	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs533726254	chr7:146730988-146730989	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs553803275	chr7:146731030-146731031	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs530801969	chr7:146731082-146731083	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs146831916	chr7:146731125-146731126	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs560905152	chr7:146731145-146731146	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs530171317	chr7:146731154-146731155	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs546684745	chr7:146731161-146731162	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs184180724	chr7:146731234-146731235	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs538840900	chr7:146731243-146731244	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs35341455	chr7:146731296-146731297	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs62484004	chr7:146731330-146731331	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs569472619	chr7:146731333-146731334	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs529753908	chr7:146731358-146731359	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs2372808	chr7:146731365-146731366	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
37	rs116897384	chr7:146731371-146731372	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs573670767	chr7:146731396-146731397	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs536400295	chr7:146731446-146731447	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs10480369	chr7:146731455-146731456	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs189974843	chr7:146731463-146731464	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs573111999	chr7:146731475-146731476	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs78899414	chr7:146731534-146731535	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs114449852	chr7:146731535-146731536	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs62484005	chr7:146731539-146731540	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs35731816	chr7:146731541-146731542	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs552480508	chr7:146731558-146731559	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs562367862	chr7:146731560-146731561	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs577289619	chr7:146731562-146731563	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs373327134	chr7:146741822-146741823	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:99)

Disease	PMID	Source
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
Medulloblastoma	21979893	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
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Wilms tumour	21544195	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
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
Renal cell carcinoma	18592004	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Multiple myeloma	17550852	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Neurodevelopmental disorder	22521361	CNVD
abortions and stillbirths	19751515	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
lymphocytic leukemia	21291569	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	16573809	CNVD
Medulloblastoma	16783165	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Glioblastoma multiforme	18628472	CNVD
abnormal development	18461090	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Papillary thyroid carcinoma	21436994	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Hodgkin''s lymphoma	18179710	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Breast cancer	16272173	CNVD
Myxofibrosarcoma	16751306	CNVD
Stuttering	21108403	CNVD
Breast cancer	17603634	CNVD
Urothelial carcinoma	18382360	CNVD
Myelodysplastic syndrome	17634407	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Multiple myeloma	16461302	CNVD
Neuroblastoma	18923191	CNVD
Breast cancer	17133270	CNVD
Schizophrenia	17646849	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Myelofibrosis	22110671	CNVD
Heart disease	21282601	CNVD
Lung adenocarcinoma	17086460	CNVD
Gastric adenocarcinoma	19115996	CNVD
Pancreatitis	21956041	CNVD
Acute myeloid leukemia	16864856	CNVD
Gastric cancer	16891809	CNVD
Lung cancer	17086460	CNVD
Autism	19546859	CNVD
Schizophrenia	19546859	CNVD
Tourette syndrome	19546859	CNVD
Cancer	20164920	CNVD
Pancreatic cancer	17952125	CNVD
Autism	20808228	CNVD
Schizophrenia	20838587	CNVD
Schizophrenia	20718829	CNVD
Neuropsychiatric disorder	21827697	CNVD
Melanoma	20877625	CNVD
Breast cancer	22522925	CNVD
Breast cancer	21509527	CNVD
Autism	20964600	CNVD
Epilepsy	17646849	CNVD
Mental retardation	19896112	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Bipolar disorder	19114987	CNVD
Cancer	20164919	CNVD
Ovarian cancer	21720365	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:287 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:146722200-146722400	Active TSS	HSMM	muscle
2	chr7:146722400-146722600	Flanking Active TSS	HSMM	muscle
3	chr7:146730800-146731600	Enhancers	Fetal Lung	lung
4	chr7:146731000-146731600	Enhancers	Ovary	ovary
5	chr7:146741800-146742800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
6	chr7:146742800-146744600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
7	chr7:146744800-146745000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
8	chr7:146746800-146747000	Enhancers	Fetal Kidney	kidney
9	chr7:146749000-146750400	Enhancers	Fetal Lung	lung
10	chr7:146749400-146749600	Enhancers	Fetal Kidney	kidney
11	chr7:146749600-146750200	Weak transcription	Fetal Kidney	kidney
12	chr7:146750200-146750400	Enhancers	Fetal Kidney	kidney
13	chr7:146750400-146753400	Weak transcription	Fetal Lung	lung
14	chr7:146751000-146751400	Enhancers	HUES64 Cell Line	embryonic stem cell
15	chr7:146751000-146751400	Enhancers	iPS-18 Cell Line	embryonic stem cell
16	chr7:146751000-146751400	Enhancers	iPS-20b Cell Line	embryonic stem cell
17	chr7:146752600-146752800	Enhancers	Gastric	stomach
18	chr7:146753400-146753600	Enhancers	Fetal Lung	lung
19	chr7:146753600-146754200	Weak transcription	Fetal Lung	lung
20	chr7:146754200-146755200	Enhancers	Fetal Lung	lung
21	chr7:146754600-146755000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
22	chr7:146756800-146757800	Enhancers	Primary hematopoietic stem cells short term culture	blood
23	chr7:146757000-146757400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
24	chr7:146757800-146758200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
25	chr7:146758200-146758400	Enhancers	Primary hematopoietic stem cells short term culture	blood
26	chr7:146758400-146760200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
27	chr7:146759600-146760200	Enhancers	Primary monocytes fromperipheralblood	blood
28	chr7:146760200-146760400	Enhancers	Primary hematopoietic stem cells short term culture	blood
29	chr7:146765800-146766200	Enhancers	Fetal Heart	heart
30	chr7:146767000-146767400	Enhancers	Pancreatic Islets	Pancreatic Islet
31	chr7:146767400-146768000	Enhancers	Fetal Lung	lung
32	chr7:146767400-146768800	Weak transcription	Pancreatic Islets	Pancreatic Islet
33	chr7:146767800-146769600	Enhancers	Fetal Kidney	kidney
34	chr7:146768800-146769000	Enhancers	Pancreatic Islets	Pancreatic Islet
35	chr7:146768800-146769400	Enhancers	Duodenum Mucosa	Duodenum
36	chr7:146769000-146769200	Enhancers	Pancreas	Pancrea
37	chr7:146769200-146780200	Weak transcription	Pancreas	Pancrea
38	chr7:146769600-146777200	Weak transcription	Fetal Kidney	kidney
39	chr7:146774800-146775600	Enhancers	Fetal Heart	heart
40	chr7:146775200-146776400	Enhancers	Fetal Brain Male	brain
41	chr7:146775600-146775800	Enhancers	Fetal Brain Female	brain
42	chr7:146775800-146778200	Weak transcription	Fetal Brain Female	brain
43	chr7:146776400-146777200	Weak transcription	Fetal Brain Male	brain
44	chr7:146777000-146777200	Enhancers	Pancreatic Islets	Pancreatic Islet
45	chr7:146777200-146777400	Enhancers	Fetal Kidney	kidney
46	chr7:146777200-146778800	Weak transcription	Pancreatic Islets	Pancreatic Islet
47	chr7:146777200-146780400	Enhancers	Fetal Brain Male	brain
48	chr7:146778200-146779400	Enhancers	Fetal Brain Female	brain
49	chr7:146778800-146779000	Weak transcription	Fetal Intestine Small	intestine
50	chr7:146778800-146779200	Active TSS	Pancreatic Islets	Pancreatic Islet

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