Variant report

Variant	esv3442720
Chromosome Location	chr7:150093044-150095992
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:14)
CpG islands
(count:246)
Chromatin interactive
region (count:10)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:14 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CCNT2	chr7:150093878-150093895	K562	blood:	n/a	n/a
2	CTCF	chr7:150094411-150094494	H1-hESC	embryonic stem cell:	n/a	n/a
3	MYC	chr7:150095983-150096002	K562	blood:	n/a	n/a
4	POLR2A	chr7:150095764-150095829	GM12878	blood:	n/a	n/a
5	POLR2A	chr7:150095767-150096906	K562	blood:	n/a	n/a
6	POLR2A	chr7:150095133-150095194	GM12878	blood:	n/a	n/a
7	POLR2A	chr7:150095295-150096103	K562	blood:	n/a	n/a
8	POLR2A	chr7:150095533-150095853	H1-hESC	embryonic stem cell:	n/a	n/a
9	POLR2A	chr7:150093117-150093181	GM12878	blood:	n/a	n/a
10	POLR2A	chr7:150095344-150095601	H1-hESC	embryonic stem cell:	n/a	n/a
11	POLR2A	chr7:150095804-150098518	K562	blood:	n/a	n/a
12	POLR2A	chr7:150093600-150093619	GM12878	blood:	n/a	n/a
13	RAD21	chr7:150094377-150094560	H1-hESC	embryonic stem cell:	n/a	n/a
14	RAD21	chr7:150094299-150094582	H1-hESC	embryonic stem cell:	n/a	n/a

(count:246 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:150095084-150095134	SK-N-SH_RA	brain:	n/a
2	chr7:150094161-150094211	SK-N-MC	brain:	n/a
3	chr7:150095084-150095134	SK-N-SH_RA	brain:	n/a
4	chr7:150094161-150094211	SK-N-MC	brain:	n/a
5	chr7:150093059-150093109	HCT-116	colon:	n/a
6	chr7:150094161-150094211	AG04450	lung:	fetal
7	chr7:150095084-150095134	Hepatocyte	liver:	n/a
8	chr7:150093059-150093109	PFSK-1	brain:	n/a
9	chr7:150094161-150094211	NT2-D1	testis:	n/a
10	chr7:150095084-150095134	PrEC	prostate:	n/a
11	chr7:150093664-150093714	ECC-1	luminal epithelium:	n/a
12	chr7:150094161-150094211	CMK	blood:	n/a
13	chr7:150095084-150095134	Caco-2	colon:	n/a
14	chr7:150095084-150095134	AG04449	skin:	fetal
15	chr7:150094161-150094211	ovcar-3	ovarian:	n/a
16	chr7:150095084-150095134	HCM	heart:	n/a
17	chr7:150093664-150093714	HCPEpiC	choroid plexus:	n/a
18	chr7:150093059-150093109	NHBE	bronchial:	n/a
19	chr7:150093664-150093714	HCF	heart:	n/a
20	chr7:150093664-150093714	BE2_C	brain:	n/a
21	chr7:150095084-150095134	HCT-116	colon:	n/a
22	chr7:150093664-150093714	SK-N-MC	brain:	n/a
23	chr7:150093664-150093714	HMEC	breast:	n/a
24	chr7:150093059-150093109	AG09309	skin:	n/a
25	chr7:150093059-150093109	HIPEpiC	eye:	n/a
26	chr7:150093664-150093714	ProgFib	skin:	n/a
27	chr7:150093059-150093109	AG04450	lung:	fetal
28	chr7:150093059-150093109	ProgFib	skin:	n/a
29	chr7:150093059-150093109	MCF10A-Er-Src	breast:	n/a
30	chr7:150094161-150094211	NB4	blood:	n/a
31	chr7:150093664-150093714	PrEC	prostate:	n/a
32	chr7:150095084-150095134	SKMC	muscle:	n/a
33	chr7:150093664-150093714	HCM	heart:	n/a
34	chr7:150093664-150093714	AG10803	skin:	n/a
35	chr7:150094161-150094211	SAEC	small airway:	n/a
36	chr7:150093059-150093109	HRPEpiC	eye:	n/a
37	chr7:150094161-150094211	AG09309	skin:	n/a
38	chr7:150093664-150093714	AG04450	lung:	fetal
39	chr7:150095084-150095134	IMR90	lung:	fetal
40	chr7:150094161-150094211	HUVEC	blood vessel:	n/a
41	chr7:150093059-150093109	BE2_C	brain:	n/a
42	chr7:150093059-150093109	AoSMC	blood vessel:	n/a
43	chr7:150094161-150094211	NHBE	bronchial:	n/a
44	chr7:150094161-150094211	ProgFib	skin:	n/a
45	chr7:150094161-150094211	HCM	heart:	n/a
46	chr7:150094161-150094211	PFSK-1	brain:	n/a
47	chr7:150094161-150094211	BE2_C	brain:	n/a
48	chr7:150095084-150095134	HMEC	breast:	n/a
49	chr7:150093059-150093109	HEEpiC	esophagus:	n/a
50	chr7:150094161-150094211	T-47D	breast:	n/a

(count:10 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:150079370..150081091-chr7:150094962..150096635,2	MCF-7	breast:
2	chr7:150063876..150080670-chr7:150093696..150109118,65	MCF-7	breast:
3	chr7:150025736..150029777-chr7:150089904..150093389,3	K562	blood:
4	chr7:150087569..150089555-chr7:150095693..150097782,2	MCF-7	breast:
5	chr7:150069152..150071203-chr7:150094833..150097484,2	MCF-7	breast:
6	chr7:150061884..150064424-chr7:150091122..150093611,2	MCF-7	breast:
7	chr7:150018966..150021782-chr7:150094675..150098930,7	K562	blood:
8	chr7:150063752..150069023-chr7:150095376..150104764,21	MCF-7	breast:
9	chr7:150073288..150077950-chr7:150093880..150099928,8	MCF-7	breast:
10	chr7:150018966..150021939-chr7:150095611..150098750,5	K562	blood:

No data

Variant related genes	Relation type
ZNF775	TF binding region
ZNF775	CpG island
ENSG00000214022	chromatin interactions
ENSG00000106526	chromatin interactions
ENSG00000240449	chromatin interactions
ENSG00000188707	chromatin interactions
ENSG00000127399	chromatin interactions
ENSG00000239377	chromatin interactions
ENSG00000196456	chromatin interactions

Extended variants
information (count: 114 )
Associated
traits (count: 89 )

Variant overlapped rSNPs/rCNVs (count:114 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs139718441	chr7:150093047-150093048	Enhancers Genic enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs565937228	chr7:150093052-150093053	Enhancers Genic enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs534628998	chr7:150093080-150093081	Enhancers Genic enhancers Weak transcription Strong transcription	CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs57508316	chr7:150093121-150093122	Enhancers Genic enhancers Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs577764786	chr7:150093137-150093138	Enhancers Genic enhancers Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs181106680	chr7:150093138-150093139	Enhancers Genic enhancers Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs556279156	chr7:150093139-150093140	Enhancers Genic enhancers Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs576012378	chr7:150093166-150093167	Enhancers Genic enhancers Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs541848822	chr7:150093198-150093199	Enhancers Genic enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs561959335	chr7:150093199-150093200	Enhancers Genic enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs528700289	chr7:150093224-150093225	Enhancers Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs143256024	chr7:150093233-150093234	Enhancers Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs184112566	chr7:150093236-150093237	Enhancers Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs60908649	chr7:150093257-150093258	Enhancers Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs541368433	chr7:150093259-150093260	Enhancers Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs56333034	chr7:150093330-150093331	Enhancers Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs533610242	chr7:150093367-150093368	Enhancers Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs144486872	chr7:150093428-150093429	Enhancers Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs529446521	chr7:150093441-150093442	Enhancers Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs145427086	chr7:150093444-150093445	Enhancers Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs551088915	chr7:150093455-150093456	Enhancers Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs188900863	chr7:150093493-150093494	Enhancers Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs149136466	chr7:150093520-150093521	Enhancers Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs565550571	chr7:150093617-150093618	Enhancers Strong transcription Weak transcription Genic enhancers ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs373538883	chr7:150093623-150093624	Enhancers Strong transcription Weak transcription Genic enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
26	rs200057340	chr7:150093648-150093649	Enhancers Strong transcription Weak transcription Genic enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
27	rs375605204	chr7:150093656-150093657	Enhancers Strong transcription Weak transcription Genic enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
28	rs551433326	chr7:150093658-150093659	Enhancers Strong transcription Weak transcription Genic enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
29	rs940453	chr7:150093701-150093702	Enhancers Strong transcription Weak transcription Genic enhancers ZNF genes & repeats	CpG island Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs536879076	chr7:150093750-150093751	Enhancers Strong transcription Weak transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs373462254	chr7:150093758-150093759	Enhancers Strong transcription Weak transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs376522510	chr7:150093779-150093780	Enhancers Strong transcription Weak transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs181687931	chr7:150093798-150093799	Enhancers Strong transcription Weak transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs199767660	chr7:150093853-150093854	Enhancers Strong transcription Weak transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs75480080	chr7:150093875-150093876	Enhancers Strong transcription Weak transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs201877119	chr7:150093891-150093892	Enhancers Strong transcription Weak transcription Genic enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
37	rs186983308	chr7:150093908-150093909	Enhancers Strong transcription Weak transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs377155143	chr7:150093929-150093930	Enhancers Strong transcription Weak transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs572349947	chr7:150093938-150093939	Enhancers Strong transcription Weak transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs541704426	chr7:150093981-150093982	Enhancers Strong transcription Weak transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs56033522	chr7:150093998-150093999	Enhancers Strong transcription Weak transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs370555977	chr7:150094012-150094013	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs375076217	chr7:150094023-150094024	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs368374618	chr7:150094028-150094029	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs371142177	chr7:150094032-150094033	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs376085338	chr7:150094080-150094081	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs368656037	chr7:150094081-150094082	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs371575884	chr7:150094100-150094101	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs564663652	chr7:150094123-150094124	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs373730918	chr7:150094128-150094129	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:89)

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
Congenital long qt syndrome	19214780	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Cancer	20164919	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:227 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:150077200-150094000	Weak transcription	Aorta	Aorta
2	chr7:150077400-150100800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
3	chr7:150077800-150093200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
4	chr7:150077800-150096000	Weak transcription	Right Atrium	heart
5	chr7:150077800-150096800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
6	chr7:150077800-150097000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
7	chr7:150078000-150100600	Weak transcription	Primary T helper cells PMA-I stimulated	--
8	chr7:150078200-150095200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
9	chr7:150078200-150097200	Weak transcription	Muscle Satellite Cultured Cells	--
10	chr7:150078200-150097200	Weak transcription	HUVEC	blood vessel
11	chr7:150078600-150096600	Weak transcription	NHEK	skin
12	chr7:150079800-150093600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
13	chr7:150079800-150095600	Weak transcription	HMEC	breast
14	chr7:150080000-150100200	Weak transcription	Primary T cells fromperipheralblood	blood
15	chr7:150080200-150093600	Weak transcription	Gastric	stomach
16	chr7:150080200-150100200	Weak transcription	Primary B cells from peripheral blood	blood
17	chr7:150080800-150096400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
18	chr7:150081000-150094800	Weak transcription	Placenta Amnion	Placenta Amnion
19	chr7:150081200-150093600	Weak transcription	Esophagus	oesophagus
20	chr7:150083000-150093800	Weak transcription	Colonic Mucosa	Colon
21	chr7:150085800-150094400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr7:150086000-150096800	Weak transcription	Osteobl	bone
23	chr7:150086200-150093200	Weak transcription	Sigmoid Colon	Sigmoid Colon
24	chr7:150086200-150096600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
25	chr7:150086400-150095000	Weak transcription	Duodenum Mucosa	Duodenum
26	chr7:150086400-150097200	Weak transcription	Stomach Mucosa	stomach
27	chr7:150086400-150100400	Weak transcription	Brain Angular Gyrus	brain
28	chr7:150086400-150100600	Weak transcription	Fetal Brain Male	brain
29	chr7:150086600-150093400	Weak transcription	Right Ventricle	heart
30	chr7:150086600-150093600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
31	chr7:150086600-150093800	Weak transcription	Left Ventricle	heart
32	chr7:150086600-150097000	Weak transcription	NH-A	brain
33	chr7:150086800-150093200	Weak transcription	Adipose Nuclei	Adipose
34	chr7:150086800-150093400	Weak transcription	Fetal Heart	heart
35	chr7:150086800-150093600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
36	chr7:150086800-150093600	Weak transcription	Brain Inferior Temporal Lobe	brain
37	chr7:150086800-150093800	Weak transcription	Brain Cingulate Gyrus	brain
38	chr7:150086800-150093800	Weak transcription	Pancreas	Pancrea
39	chr7:150086800-150094400	Weak transcription	Brain Substantia Nigra	brain
40	chr7:150086800-150095200	Weak transcription	Colon Smooth Muscle	Colon
41	chr7:150086800-150101000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
42	chr7:150087000-150101200	Weak transcription	Liver	Liver
43	chr7:150087400-150093600	Weak transcription	Skeletal Muscle Male	skeletal muscle
44	chr7:150087400-150095800	Weak transcription	Psoas Muscle	Psoas
45	chr7:150087400-150097000	Weak transcription	HepG2	liver
46	chr7:150087600-150093600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
47	chr7:150087600-150095600	Weak transcription	Skeletal Muscle Female	skeletal muscle
48	chr7:150088000-150093200	Weak transcription	Thymus	Thymus
49	chr7:150088000-150093400	Weak transcription	Duodenum Smooth Muscle	Duodenum
50	chr7:150088000-150093600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin

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