Variant report

Variant	nsv889475
Chromosome Location	chr7:150729212-150742700
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:474)
CpG islands
(count:671)
Chromatin interactive
region (count:3)
LncRNA
region (count:12)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:474 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

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	chr7:150736082-150736896	A549	lung:	n/a	n/a
7	BCL3	chr7:150735968-150736723	A549	lung:	n/a	n/a
8	BHLHE40	chr7:150736000-150737271	K562	blood:	n/a	n/a
9	BHLHE40	chr7:150730208-150730254	K562	blood:	n/a	n/a
10	CBX3	chr7:150736256-150737110	K562	blood:	n/a	n/a
11	CBX3	chr7:150735857-150737562	K562	blood:	n/a	n/a
12	CCNT2	chr7:150736179-150737490	K562	blood:	n/a	n/a
13	CEBPB	chr7:150736416-150736741	K562	blood:	n/a	n/a
14	CEBPB	chr7:150735516-150735627	K562	blood:	n/a	n/a
15	CEBPB	chr7:150736273-150737014	K562	blood:	n/a	n/a
16	CEBPB	chr7:150735450-150735654	A549	lung:	n/a	n/a
17	CEBPB	chr7:150735520-150735588	Hela-S3	cervix:	n/a	n/a
18	CEBPD	chr7:150736267-150736978	K562	blood:	n/a	n/a
19	CHD2	chr7:150736329-150736759	Hela-S3	cervix:	n/a	n/a
20	CHD2	chr7:150739386-150739395	K562	blood:	n/a	n/a
21	CHD2	chr7:150736109-150736964	K562	blood:	n/a	n/a
22	CTCF	chr7:150730180-150730330	HEK293	kidney:	n/a	n/a
23	CTCF	chr7:150739393-150739465	MCF-7	breast:	n/a	n/a
24	CTCF	chr7:150730080-150730230	GM12872	blood:	n/a	n/a
25	CTCF	chr7:150730080-150730230	A549	lung:	n/a	n/a
26	CTCF	chr7:150730048-150730380	K562	blood:	n/a	n/a
27	CTCF	chr7:150730078-150730379	H1-hESC	embryonic stem cell:	n/a	n/a
28	CTCF	chr7:150730161-150730291	IMR90	lung:	n/a	n/a
29	CTCF	chr7:150736540-150736690	A549	lung:	n/a	n/a
30	CTCF	chr7:150730120-150730270	HEK293	kidney:	n/a	n/a
31	CTCF	chr7:150737040-150737190	NB4	blood:	n/a	n/a
32	CTCF	chr7:150730180-150730330	NHEK	skin:	n/a	n/a
33	CTCF	chr7:150730100-150730250	RPTEC	kidney:	n/a	n/a
34	CTCF	chr7:150730120-150730270	GM12875	blood:	n/a	n/a
35	CTCF	chr7:150730170-150730263	HepG2	liver:	n/a	n/a
36	CTCF	chr7:150730132-150730308	K562	blood:	n/a	n/a
37	CTCF	chr7:150730140-150730290	Caco-2	colon:	n/a	n/a
38	CTCF	chr7:150730120-150730270	SAEC	small airway:	n/a	n/a
39	CTCF	chr7:150730183-150730192	GM12878	blood:	n/a	n/a
40	CTCF	chr7:150739402-150739479	MCF-7	breast:	n/a	n/a
41	CTCF	chr7:150730089-150730329	HepG2	liver:	n/a	n/a
42	CTCF	chr7:150737120-150737270	BE2_C	brain:	n/a	n/a
43	CTCF	chr7:150729928-150730483	K562	blood:	n/a	n/a
44	CTCF	chr7:150737120-150737270	WERI-Rb-1	eye:	n/a	n/a
45	CTCF	chr7:150730120-150730270	Hela-S3	cervix:	n/a	n/a
46	CTCF	chr7:150730100-150730250	HRE	kidney:	n/a	n/a
47	CTCF	chr7:150730080-150730230	BJ	skin:	n/a	n/a
48	CTCF	chr7:150730047-150730385	K562	blood:	n/a	n/a
49	CTCF	chr7:150730203-150730236	GM19239	blood:	n/a	n/a
50	CTCF	chr7:150730197-150730236	GM12892	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	chr7:150742459-150742509	NB4	blood:	n/a
2	chr7:150733014-150733064	NHDF-neo	bronchial:	n/a
3	chr7:150738304-150738354	GM06990	blood:	n/a
4	chr7:150732834-150732884	Caco-2	colon:	n/a
5	chr7:150733014-150733064	HCF	heart:	n/a
6	chr7:150739712-150739762	HRE	kidney:	n/a
7	chr7:150741207-150741257	SK-N-MC	brain:	n/a
8	chr7:150741207-150741257	Hela-S3	cervix:	n/a
9	chr7:150736638-150736688	GM12891	blood:	n/a
10	chr7:150739712-150739762	HAEpiC	amniotic membrane:	n/a
11	chr7:150741297-150741347	HEK293	kidney:	embryo
12	chr7:150742459-150742509	HEK293	kidney:	embryo
13	chr7:150736638-150736688	HRCEpiC	kidney:	n/a
14	chr7:150736638-150736688	K562	blood:	n/a
15	chr7:150741161-150741211	HEK293	kidney:	embryo
16	chr7:150741161-150741211	HRPEpiC	eye:	n/a
17	chr7:150732834-150732884	HCF	heart:	n/a
18	chr7:150741207-150741257	GM06990	blood:	n/a
19	chr7:150738304-150738354	HCT-116	colon:	n/a
20	chr7:150733014-150733064	NHBE	bronchial:	n/a
21	chr7:150741161-150741211	PANC-1	pancreas:	n/a
22	chr7:150741161-150741211	ECC-1	luminal epithelium:	n/a
23	chr7:150736638-150736688	U87	brain:	n/a
24	chr7:150741297-150741347	RPTEC	kidney:	n/a
25	chr7:150739712-150739762	HMEC	breast:	n/a
26	chr7:150737198-150737248	SKMC	muscle:	n/a
27	chr7:150741207-150741257	ovcar-3	ovarian:	n/a
28	chr7:150733014-150733064	AG09309	skin:	n/a
29	chr7:150733014-150733064	HRE	kidney:	n/a
30	chr7:150733014-150733064	HCPEpiC	choroid plexus:	n/a
31	chr7:150737198-150737248	HUVEC	blood vessel:	n/a
32	chr7:150741207-150741257	NT2-D1	testis:	n/a
33	chr7:150738304-150738354	K562	blood:	n/a
34	chr7:150741297-150741347	HL-60	blood:	n/a
35	chr7:150736638-150736688	NH-A	brain:	n/a
36	chr7:150741096-150741146	SAEC	small airway:	n/a
37	chr7:150737198-150737248	GM06990	blood:	n/a
38	chr7:150741207-150741257	U87	brain:	n/a
39	chr7:150741161-150741211	IMR90	lung:	fetal
40	chr7:150733014-150733064	SK-N-SH	brain:	n/a
41	chr7:150738304-150738354	ProgFib	skin:	n/a
42	chr7:150732834-150732884	GM12892	blood:	n/a
43	chr7:150732834-150732884	IMR90	lung:	fetal
44	chr7:150732834-150732884	HCT-116	colon:	n/a
45	chr7:150741207-150741257	HL-60	blood:	n/a
46	chr7:150741297-150741347	Hela-S3	cervix:	n/a
47	chr7:150742459-150742509	ovcar-3	ovarian:	n/a
48	chr7:150741207-150741257	AG09319	gingival:	n/a
49	chr7:150738304-150738354	GM19239	blood:	n/a
50	chr7:150741161-150741211	MCF10A-Er-Src	breast:	n/a

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

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

(count:12 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ACCN3-2	chr7:150739649-150739806	l_3508_chr7:150739648-150741401_prostate
2	lnc-NOS3-1	chr7:150730530-150730691	NONHSAT124170
3	lnc-NOS3-1	chr7:150729931-150730121	NONHSAT124171
4	lnc-NOS3-1	chr7:150731592-150731686	NONHSAT124170
5	lnc-ACCN3-2	chr7:150741291-150741401	l_3508_chr7:150739648-150741401_prostate
6	lnc-NOS3-1	chr7:150730692-150730785	NONHSAT124175
7	lnc-NOS3-1	chr7:150730692-150730837	NONHSAT124169
8	lnc-ACCN3-2	chr7:150739969-150740089	l_3508_chr7:150739648-150741401_prostate
9	lnc-NOS3-1	chr7:150729931-150730147	NONHSAT124176
10	lnc-ACCN3-2	chr7:150740738-150740871	l_3508_chr7:150739648-150741401_prostate
11	lnc-NOS3-1	chr7:150729931-150730329	NONHSAT124172
12	lnc-NOS3-1	chr7:150731360-150731515	NONHSAT124170

No data

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

Extended variants
information (count: 719 )
Associated
traits (count: 87 )

Variant overlapped rSNPs/rCNVs (count:719 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6947821	chr7:150729212-150729213	Weak transcription Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs553312137	chr7:150729228-150729229	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs374217747	chr7:150729261-150729262	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs542609079	chr7:150729270-150729271	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs552978123	chr7:150729280-150729281	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs527347412	chr7:150729341-150729342	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs572985460	chr7:150729386-150729387	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs545119904	chr7:150729388-150729389	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs565044221	chr7:150729433-150729434	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs368119699	chr7:150729440-150729441	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs544433841	chr7:150729460-150729461	Weak transcription Strong transcription Genic enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
12	rs561021047	chr7:150729461-150729462	Weak transcription Strong transcription Genic enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
13	rs185590174	chr7:150729466-150729467	Weak transcription Strong transcription Genic enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
14	rs563515145	chr7:150729491-150729492	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs148447324	chr7:150729559-150729560	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs566486543	chr7:150729572-150729573	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs532219917	chr7:150729591-150729592	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs375178158	chr7:150729602-150729603	Weak transcription Strong transcription Genic enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
19	rs551991461	chr7:150729614-150729615	Weak transcription Strong transcription Genic enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
20	rs190441060	chr7:150729619-150729620	Weak transcription Strong transcription Genic enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
21	rs537240017	chr7:150729658-150729659	Weak transcription Strong transcription Genic enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
22	rs141263065	chr7:150729684-150729685	Weak transcription Strong transcription Genic enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
23	rs557580586	chr7:150729694-150729695	Weak transcription Strong transcription Genic enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
24	rs567598668	chr7:150729725-150729726	Weak transcription Strong transcription Genic enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
25	rs141787570	chr7:150729762-150729763	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs11983731	chr7:150729768-150729769	Weak transcription Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs80024623	chr7:150729780-150729781	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs376420683	chr7:150729793-150729794	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs372624691	chr7:150729794-150729795	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs572904127	chr7:150729804-150729805	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs139972021	chr7:150729818-150729819	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs574673233	chr7:150729819-150729820	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs558772258	chr7:150729845-150729846	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs575738105	chr7:150729851-150729852	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs182766869	chr7:150729890-150729891	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs369535254	chr7:150729935-150729936	Weak transcription Strong transcription Genic enhancers	TF binding region lncRNA	2 gene(s)	Overlapped CNVs	n/a
37	rs561168445	chr7:150729957-150729958	Weak transcription Strong transcription Genic enhancers	TF binding region lncRNA	2 gene(s)	Overlapped CNVs	n/a
38	rs373122552	chr7:150730071-150730072	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region lncRNA	2 gene(s)	Overlapped CNVs	n/a
39	rs188746378	chr7:150730076-150730077	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region lncRNA	2 gene(s)	Overlapped CNVs	n/a
40	rs193013654	chr7:150730115-150730116	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region lncRNA	2 gene(s)	Overlapped CNVs	n/a
41	rs542089386	chr7:150730153-150730154	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region lncRNA	2 gene(s)	Overlapped CNVs	n/a
42	rs10952299	chr7:150730220-150730221	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region lncRNA	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
43	rs532157238	chr7:150730254-150730255	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region lncRNA	2 gene(s)	Overlapped CNVs	n/a
44	rs567405424	chr7:150730259-150730260	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region lncRNA	2 gene(s)	Overlapped CNVs	n/a
45	rs184097473	chr7:150730284-150730285	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region lncRNA	2 gene(s)	Overlapped CNVs	n/a
46	rs570815146	chr7:150730286-150730287	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region lncRNA	2 gene(s)	Overlapped CNVs	n/a
47	rs562440991	chr7:150730315-150730316	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region lncRNA	2 gene(s)	Overlapped CNVs	n/a
48	rs76866700	chr7:150730412-150730413	Weak transcription Strong transcription Genic enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
49	rs531465274	chr7:150730482-150730483	Weak transcription Strong transcription Genic enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
50	rs561344040	chr7:150730484-150730485	Weak transcription Strong transcription Genic enhancers	TF binding region	2 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:639 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:150726000-150730000	Weak transcription	Gastric	stomach
2	chr7:150726200-150731800	Weak transcription	Aorta	Aorta
3	chr7:150726200-150735800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
4	chr7:150726400-150729800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
5	chr7:150726400-150729800	Weak transcription	Spleen	Spleen
6	chr7:150726400-150730000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
7	chr7:150726400-150730000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
8	chr7:150726400-150730000	Weak transcription	Ovary	ovary
9	chr7:150726400-150730600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
10	chr7:150726400-150731400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
11	chr7:150726400-150731400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
12	chr7:150726400-150731600	Weak transcription	HUES48 Cell Line	embryonic stem cell
13	chr7:150726400-150731600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
14	chr7:150726400-150731800	Weak transcription	H1 Cell Line	embryonic stem cell
15	chr7:150726400-150732000	Weak transcription	H9 Cell Line	embryonic stem cell
16	chr7:150726400-150735800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
17	chr7:150726400-150736600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr7:150726400-150743600	Weak transcription	Fetal Kidney	kidney
19	chr7:150726400-150744200	Weak transcription	Right Atrium	heart
20	chr7:150726400-150745000	Weak transcription	Pancreatic Islets	Pancreatic Islet
21	chr7:150726600-150729800	Weak transcription	Muscle Satellite Cultured Cells	--
22	chr7:150726600-150730000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chr7:150726600-150730200	Weak transcription	Stomach Smooth Muscle	stomach
24	chr7:150726600-150730200	Weak transcription	NHLF	lung
25	chr7:150726600-150730400	Weak transcription	Adipose Nuclei	Adipose
26	chr7:150726600-150730400	Weak transcription	Colonic Mucosa	Colon
27	chr7:150726600-150731000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
28	chr7:150726600-150731000	Weak transcription	Rectal Mucosa Donor 31	rectum
29	chr7:150726600-150731400	Weak transcription	HUES6 Cell Line	embryonic stem cell
30	chr7:150726600-150731400	Weak transcription	Primary neutrophils fromperipheralblood	blood
31	chr7:150726600-150731400	Weak transcription	HSMMtube	muscle
32	chr7:150726600-150731800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
33	chr7:150726600-150731800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
34	chr7:150726600-150731800	Weak transcription	Primary B cells from cord blood	blood
35	chr7:150726600-150731800	Weak transcription	Small Intestine	intestine
36	chr7:150726600-150731800	Weak transcription	Monocytes-CD14+_RO01746	blood
37	chr7:150726600-150733000	Weak transcription	HUES64 Cell Line	embryonic stem cell
38	chr7:150726600-150735800	Weak transcription	Primary hematopoietic stem cells	blood
39	chr7:150726600-150736000	Weak transcription	Fetal Heart	heart
40	chr7:150726600-150736000	Weak transcription	HepG2	liver
41	chr7:150726600-150736200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
42	chr7:150726600-150745400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
43	chr7:150726800-150730200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
44	chr7:150726800-150735000	Weak transcription	NHDF-Ad	bronchial
45	chr7:150727000-150729400	Weak transcription	Brain Cingulate Gyrus	brain
46	chr7:150727000-150729800	Weak transcription	Lung	lung
47	chr7:150727000-150730000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
48	chr7:150727000-150730000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
49	chr7:150727000-150730000	Weak transcription	Liver	Liver
50	chr7:150727000-150730000	Weak transcription	Fetal Thymus	thymus

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