Variant report

Variant	nsv609011
Chromosome Location	chr7:150731698-150743820
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:418)
CpG islands
(count:671)
Chromatin interactive
region (count:4)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:418 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:150736210-150737016	K562	blood:	n/a	n/a
2	ATF1	chr7:150736197-150736751	K562	blood:	n/a	n/a
3	ATF3	chr7:150736152-150736869	K562	blood:	n/a	n/a
4	ATF3	chr7:150736085-150736712	K562	blood:	n/a	n/a
5	BACH1	chr7:150736342-150736841	K562	blood:	n/a	n/a
6	BCL3	chr7:150735968-150736723	A549	lung:	n/a	n/a
7	BCL3	chr7:150736082-150736896	A549	lung:	n/a	n/a
8	BHLHE40	chr7:150736000-150737271	K562	blood:	n/a	n/a
9	CBX3	chr7:150735857-150737562	K562	blood:	n/a	n/a
10	CBX3	chr7:150736256-150737110	K562	blood:	n/a	n/a
11	CCNT2	chr7:150736179-150737490	K562	blood:	n/a	n/a
12	CEBPB	chr7:150736273-150737014	K562	blood:	n/a	n/a
13	CEBPB	chr7:150735450-150735654	A549	lung:	n/a	n/a
14	CEBPB	chr7:150735520-150735588	Hela-S3	cervix:	n/a	n/a
15	CEBPB	chr7:150736416-150736741	K562	blood:	n/a	n/a
16	CEBPB	chr7:150735516-150735627	K562	blood:	n/a	n/a
17	CEBPD	chr7:150736267-150736978	K562	blood:	n/a	n/a
18	CHD2	chr7:150736329-150736759	Hela-S3	cervix:	n/a	n/a
19	CHD2	chr7:150736109-150736964	K562	blood:	n/a	n/a
20	CHD2	chr7:150739386-150739395	K562	blood:	n/a	n/a
21	CTCF	chr7:150736353-150737256	K562	blood:	n/a	n/a
22	CTCF	chr7:150736320-150736470	AoAF	blood vessel:	n/a	n/a
23	CTCF	chr7:150736320-150736470	HUVEC	blood vessel:	n/a	n/a
24	CTCF	chr7:150736300-150736450	NHDF-neo	bronchial:	n/a	n/a
25	CTCF	chr7:150739402-150739479	MCF-7	breast:	n/a	n/a
26	CTCF	chr7:150737120-150737270	WERI-Rb-1	eye:	n/a	n/a
27	CTCF	chr7:150737040-150737190	NB4	blood:	n/a	n/a
28	CTCF	chr7:150739360-150739510	HepG2	liver:	n/a	n/a
29	CTCF	chr7:150736922-150737444	K562	blood:	n/a	n/a
30	CTCF	chr7:150739389-150739455	MCF-7	breast:	n/a	n/a
31	CTCF	chr7:150737145-150737253	K562	blood:	n/a	n/a
32	CTCF	chr7:150737120-150737270	BE2_C	brain:	n/a	n/a
33	CTCF	chr7:150737080-150737230	HUVEC	blood vessel:	n/a	n/a
34	CTCF	chr7:150736280-150736430	NHDF-neo	bronchial:	n/a	n/a
35	CTCF	chr7:150739393-150739465	MCF-7	breast:	n/a	n/a
36	CTCF	chr7:150736260-150736410	AoAF	blood vessel:	n/a	n/a
37	CTCF	chr7:150737160-150737310	SK-N-SH_RA	brain:	n/a	n/a
38	CTCF	chr7:150736540-150736690	A549	lung:	n/a	n/a
39	CTCF	chr7:150739375-150739487	MCF-7	breast:	n/a	n/a
40	CTCF	chr7:150737033-150737314	K562	blood:	n/a	n/a
41	CTCF	chr7:150736300-150736450	AG04449	skin:	n/a	n/a
42	CUX1	chr7:150735904-150737206	K562	blood:	n/a	n/a
43	E2F4	chr7:150736167-150737229	K562	blood:	n/a	n/a
44	E2F4	chr7:150736530-150736728	MCF10A-Er-Src	breast:	n/a	n/a
45	E2F6	chr7:150736318-150737151	A549	lung:	n/a	n/a
46	E2F6	chr7:150736093-150736323	K562	blood:	n/a	n/a
47	EGR1	chr7:150736187-150737568	K562	blood:	n/a	chr7:150737466-150737479
48	EGR1	chr7:150736093-150737524	K562	blood:	n/a	chr7:150737466-150737479
49	ELF1	chr7:150736117-150736767	K562	blood:	n/a	n/a
50	ELF1	chr7:150736779-150737400	K562	blood:	n/a	n/a

(count:671 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:150737198-150737248	ECC-1	luminal epithelium:	n/a
2	chr7:150737198-150737248	SK-N-SH	brain:	n/a
3	chr7:150733014-150733064	GM19239	blood:	n/a
4	chr7:150741096-150741146	PFSK-1	brain:	n/a
5	chr7:150739712-150739762	IMR90	lung:	fetal
6	chr7:150741161-150741211	HPAEpiC	pulmonary alveolar:	n/a
7	chr7:150741207-150741257	AG04449	skin:	fetal
8	chr7:150733014-150733064	HepG2	liver:	n/a
9	chr7:150732834-150732884	ovcar-3	ovarian:	n/a
10	chr7:150741161-150741211	HMEC	breast:	n/a
11	chr7:150738304-150738354	MCF10A-Er-Src	breast:	n/a
12	chr7:150742459-150742509	H1-hESC	embryonic stem cell:	embryo
13	chr7:150737198-150737248	PrEC	prostate:	n/a
14	chr7:150738304-150738354	AG09319	gingival:	n/a
15	chr7:150741297-150741347	GM12891	blood:	n/a
16	chr7:150738304-150738354	SK-N-MC	brain:	n/a
17	chr7:150737198-150737248	NH-A	brain:	n/a
18	chr7:150732834-150732884	Hela-S3	cervix:	n/a
19	chr7:150737198-150737248	HCPEpiC	choroid plexus:	n/a
20	chr7:150741297-150741347	SK-N-SH	brain:	n/a
21	chr7:150741297-150741347	GM06990	blood:	n/a
22	chr7:150742459-150742509	PrEC	prostate:	n/a
23	chr7:150742459-150742509	HRCEpiC	kidney:	n/a
24	chr7:150741096-150741146	HEK293	kidney:	embryo
25	chr7:150732834-150732884	PANC-1	pancreas:	n/a
26	chr7:150741096-150741146	SAEC	small airway:	n/a
27	chr7:150741207-150741257	T-47D	breast:	n/a
28	chr7:150736638-150736688	GM12878	blood:	n/a
29	chr7:150733014-150733064	CMK	blood:	n/a
30	chr7:150741207-150741257	GM12878	blood:	n/a
31	chr7:150742459-150742509	SK-N-MC	brain:	n/a
32	chr7:150737198-150737248	HMEC	breast:	n/a
33	chr7:150733014-150733064	HUVEC	blood vessel:	n/a
34	chr7:150739712-150739762	HIPEpiC	eye:	n/a
35	chr7:150741096-150741146	A549	lung:	n/a
36	chr7:150741207-150741257	NH-A	brain:	n/a
37	chr7:150742459-150742509	AG10803	skin:	n/a
38	chr7:150741161-150741211	HL-60	blood:	n/a
39	chr7:150732834-150732884	GM12878	blood:	n/a
40	chr7:150732834-150732884	GM12891	blood:	n/a
41	chr7:150741207-150741257	ProgFib	skin:	n/a
42	chr7:150738304-150738354	PrEC	prostate:	n/a
43	chr7:150733014-150733064	HEK293	kidney:	embryo
44	chr7:150741096-150741146	Hepatocyte	liver:	n/a
45	chr7:150737198-150737248	NT2-D1	testis:	n/a
46	chr7:150739712-150739762	AG10803	skin:	n/a
47	chr7:150741297-150741347	HMEC	breast:	n/a
48	chr7:150742459-150742509	GM12891	blood:	n/a
49	chr7:150741297-150741347	HL-60	blood:	n/a
50	chr7:150741207-150741257	ovcar-3	ovarian:	n/a

(count:4 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:150743382..150745288-chr7:151545061..151547871,2	MCF-7	breast:
2	chr11:118795468..118797333-chr7:150736370..150738345,2	MCF-7	breast:
3	chr7:150736857..150739540-chr7:150928715..150930343,2	MCF-7	breast:
4	chr7:150739594..150740120-chr7:150753037..150753552,2	K562	blood:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ACCN3-2	chr7:150740738-150740871	l_3508_chr7:150739648-150741401_prostate
2	lnc-ACCN3-2	chr7:150741291-150741401	l_3508_chr7:150739648-150741401_prostate
3	lnc-ACCN3-2	chr7:150739969-150740089	l_3508_chr7:150739648-150741401_prostate
4	lnc-ACCN3-2	chr7:150739649-150739806	l_3508_chr7:150739648-150741401_prostate

No data

Variant related genes	Relation type
ASIC3	TF binding region
ABCB8	TF binding region
ENSG00000243433	TF binding region
ASIC3	CpG island
ABCB8	CpG island
ENSG00000243433	CpG island
ENSG00000033100	chromatin interactions
ENSG00000164885	chromatin interactions
ENSG00000186174	chromatin interactions
ENSG00000110375	chromatin interactions

Extended variants
information (count: 643 )
Associated
traits (count: 87 )

Variant overlapped rSNPs/rCNVs (count:643 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2303924	chr7:150731698-150731699	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs553976897	chr7:150731704-150731705	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
3	rs199833241	chr7:150731705-150731706	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
4	rs35489220	chr7:150731736-150731737	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
5	rs367793580	chr7:150731737-150731738	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
6	rs539313810	chr7:150731741-150731742	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
7	rs556413222	chr7:150731744-150731745	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
8	rs374538950	chr7:150731782-150731783	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
9	rs61734192	chr7:150731815-150731816	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs367609308	chr7:150731820-150731821	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs202068976	chr7:150731832-150731833	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs149107087	chr7:150731874-150731875	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs371362143	chr7:150731905-150731906	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs576303853	chr7:150731991-150731992	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs188533468	chr7:150732020-150732021	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs574907803	chr7:150732031-150732032	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs552675927	chr7:150732032-150732033	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs377682654	chr7:150732093-150732094	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs554976199	chr7:150732136-150732137	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs575101923	chr7:150732146-150732147	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs79292147	chr7:150732175-150732176	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs540746199	chr7:150732203-150732204	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs142398497	chr7:150732215-150732216	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs532753080	chr7:150732227-150732228	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs546124117	chr7:150732249-150732250	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs563195917	chr7:150732291-150732292	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs376265324	chr7:150732302-150732303	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs377014586	chr7:150732311-150732312	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs548588911	chr7:150732329-150732330	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs568483242	chr7:150732333-150732334	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs527757918	chr7:150732348-150732349	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs547915529	chr7:150732354-150732355	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs374263113	chr7:150732355-150732356	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs570896724	chr7:150732360-150732361	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs368195297	chr7:150732423-150732424	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs539616958	chr7:150732428-150732429	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs563580732	chr7:150732447-150732448	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs2303925	chr7:150732463-150732464	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs191844882	chr7:150732486-150732487	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs535374754	chr7:150732512-150732513	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs374102707	chr7:150732518-150732519	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs367552631	chr7:150732542-150732543	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs571708224	chr7:150732600-150732601	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs372401926	chr7:150732623-150732624	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs184975044	chr7:150732627-150732628	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs41282730	chr7:150732630-150732631	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs117517576	chr7:150732634-150732635	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs372442090	chr7:150732647-150732648	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs76884999	chr7:150732649-150732650	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs369818772	chr7:150732674-150732675	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:87)

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
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	17603634	CNVD
Urothelial carcinoma	18382360	CNVD
Myelodysplastic syndrome	17634407	CNVD
Multiple myeloma	16461302	CNVD
Neuroblastoma	18923191	CNVD
Schizophrenia	17646849	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Acute myeloid leukemia	16864856	CNVD
Autism	20808228	CNVD
Breast cancer	21509527	CNVD
Ovarian cancer	21720365	CNVD
Heart disease	21282601	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	21045282	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Glioblastoma multiforme	17002787	CNVD
Lobular carcinoma	20920651	CNVD
Long-qt syndrome	20920651	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Liver carcinoma	19366792	CNVD
Long-qt syndrome	17576883	CNVD
Bradycardia syndrome	17576883	CNVD
Sudden cardiac death	19188705	CNVD
renal disease	17924346	CNVD
Ovarian cancer	21781307	CNVD
Adrenocortical carcinoma	18281524	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:644 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:150726200-150731800	Weak transcription	Aorta	Aorta
2	chr7:150726200-150735800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
3	chr7:150726400-150731800	Weak transcription	H1 Cell Line	embryonic stem cell
4	chr7:150726400-150732000	Weak transcription	H9 Cell Line	embryonic stem cell
5	chr7:150726400-150735800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
6	chr7:150726400-150736600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr7:150726400-150743600	Weak transcription	Fetal Kidney	kidney
8	chr7:150726400-150744200	Weak transcription	Right Atrium	heart
9	chr7:150726400-150745000	Weak transcription	Pancreatic Islets	Pancreatic Islet
10	chr7:150726600-150731800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
11	chr7:150726600-150731800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
12	chr7:150726600-150731800	Weak transcription	Primary B cells from cord blood	blood
13	chr7:150726600-150731800	Weak transcription	Small Intestine	intestine
14	chr7:150726600-150731800	Weak transcription	Monocytes-CD14+_RO01746	blood
15	chr7:150726600-150733000	Weak transcription	HUES64 Cell Line	embryonic stem cell
16	chr7:150726600-150735800	Weak transcription	Primary hematopoietic stem cells	blood
17	chr7:150726600-150736000	Weak transcription	Fetal Heart	heart
18	chr7:150726600-150736000	Weak transcription	HepG2	liver
19	chr7:150726600-150736200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
20	chr7:150726600-150745400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
21	chr7:150726800-150735000	Weak transcription	NHDF-Ad	bronchial
22	chr7:150727000-150731800	Weak transcription	Left Ventricle	heart
23	chr7:150727000-150731800	Weak transcription	HMEC	breast
24	chr7:150727000-150733400	Weak transcription	NH-A	brain
25	chr7:150727000-150735600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
26	chr7:150727000-150735600	Weak transcription	HUVEC	blood vessel
27	chr7:150727000-150746400	Weak transcription	Fetal Brain Male	brain
28	chr7:150727200-150731800	Weak transcription	A549	lung
29	chr7:150727200-150732000	Weak transcription	Fetal Lung	lung
30	chr7:150727200-150733400	Weak transcription	Hela-S3	cervix
31	chr7:150727200-150736600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
32	chr7:150727400-150731800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
33	chr7:150727800-150744400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
34	chr7:150728000-150734600	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
35	chr7:150728000-150734600	Strong transcription	Duodenum Mucosa	Duodenum
36	chr7:150728000-150735200	Strong transcription	Primary T cells from cord blood	blood
37	chr7:150728000-150735200	Strong transcription	Sigmoid Colon	Sigmoid Colon
38	chr7:150728200-150735000	Strong transcription	Dnd41	blood
39	chr7:150728200-150735200	Strong transcription	Primary T helper cells fromperipheralblood	blood
40	chr7:150728200-150735800	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
41	chr7:150728200-150736000	Strong transcription	Breast Myoepithelial Primary Cells	Breast
42	chr7:150728200-150736400	Weak transcription	GM12878-XiMat	blood
43	chr7:150728400-150732000	Strong transcription	Right Ventricle	heart
44	chr7:150728400-150734400	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
45	chr7:150728400-150735000	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
46	chr7:150728400-150735000	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
47	chr7:150728400-150735600	Strong transcription	Fetal Intestine Small	intestine
48	chr7:150728400-150735600	Strong transcription	Fetal Muscle Trunk	muscle
49	chr7:150728400-150735800	Strong transcription	Fetal Muscle Leg	muscle
50	chr7:150728600-150732000	Weak transcription	Placenta Amnion	Placenta Amnion

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