Variant report

Variant	nsv594902
Chromosome Location	chr4:95679013-95679796
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr4:95679125-95679401	H1-hESC	embryonic stem cell:	n/a	n/a
2	CHD1	chr4:95677993-95680028	IMR90	lung:	n/a	chr4:95679126-95679136 chr4:95679131-95679141
3	CHD2	chr4:95678813-95679126	H1-hESC	embryonic stem cell:	n/a	n/a
4	CREB1	chr4:95678728-95679047	A549	lung:	n/a	n/a
5	CTBP2	chr4:95678812-95680327	H1-hESC	embryonic stem cell:	n/a	n/a
6	CTCF	chr4:95678940-95679090	NHDF-neo	bronchial:	n/a	n/a
7	CTCF	chr4:95678900-95679050	AG09319	gingival:	n/a	n/a
8	CTCF	chr4:95678900-95679050	SK-N-SH_RA	brain:	n/a	n/a
9	CTCF	chr4:95678900-95679050	HMEC	breast:	n/a	n/a
10	CTCF	chr4:95678880-95679030	HEEpiC	esophagus:	n/a	n/a
11	CTCF	chr4:95678791-95679131	IMR90	lung:	n/a	n/a
12	CTCF	chr4:95678900-95679050	SAEC	small airway:	n/a	n/a
13	CTCF	chr4:95678900-95679050	HAc	cerebellar:	n/a	n/a
14	CTCF	chr4:95678920-95679070	NHDF-neo	bronchial:	n/a	n/a
15	CTCF	chr4:95678880-95679030	AG10803	skin:	n/a	n/a
16	CTCF	chr4:95678900-95679050	RPTEC	kidney:	n/a	n/a
17	CTCF	chr4:95678900-95679050	AG09309	skin:	n/a	n/a
18	CTCF	chr4:95678900-95679050	NHLF	lung:	n/a	n/a
19	CTCF	chr4:95678900-95679050	BE2_C	brain:	n/a	n/a
20	CTCF	chr4:95678880-95679030	HRPEpiC	eye:	n/a	n/a
21	CTCF	chr4:95678920-95679070	HRE	kidney:	n/a	n/a
22	CTCF	chr4:95678920-95679070	HPAF	blood vessel:	n/a	n/a
23	CTCF	chr4:95678900-95679050	HRPEpiC	eye:	n/a	n/a
24	CTCF	chr4:95678850-95679013	SK-N-SH_RA	brain:	n/a	n/a
25	CTCF	chr4:95678940-95679090	HFF	foreskin:	n/a	n/a
26	CTCF	chr4:95678880-95679030	MCF-7	breast:	n/a	n/a
27	CTCF	chr4:95678841-95679015	ProgFib	skin:	n/a	n/a
28	CTCF	chr4:95678900-95679050	WI-38	lung:	n/a	n/a
29	CTCF	chr4:95678920-95679070	HA-sp	spinal cord:	n/a	n/a
30	CTCF	chr4:95678880-95679030	HPAF	blood vessel:	n/a	n/a
31	CTCF	chr4:95678875-95679031	Medullo	brain:	n/a	n/a
32	E2F4	chr4:95678657-95679124	MCF10A-Er-Src	breast:	n/a	n/a
33	E2F6	chr4:95679062-95680154	H1-hESC	embryonic stem cell:	n/a	chr4:95679542-95679552 chr4:95679544-95679553 chr4:95679618-95679630 chr4:95679539-95679549
34	E2F6	chr4:95679385-95679616	K562	blood:	n/a	chr4:95679542-95679552 chr4:95679544-95679553 chr4:95679539-95679549
35	E2F6	chr4:95678772-95680183	H1-hESC	embryonic stem cell:	n/a	chr4:95679542-95679552 chr4:95679544-95679553 chr4:95679618-95679630 chr4:95679539-95679549
36	E2F6	chr4:95679308-95679784	A549	lung:	n/a	chr4:95679542-95679552 chr4:95679544-95679553 chr4:95679618-95679630 chr4:95679539-95679549
37	EP300	chr4:95678767-95679081	SK-N-SH_RA	brain:	n/a	chr4:95678846-95678862
38	FOSL2	chr4:95679587-95680387	A549	lung:	n/a	chr4:95679676-95679685 chr4:95680374-95680384
39	FOXP2	chr4:95679032-95679849	PFSK-1	brain:	n/a	n/a
40	GABPA	chr4:95679182-95679665	H1-hESC	embryonic stem cell:	n/a	chr4:95679516-95679525
41	GTF2F1	chr4:95679428-95679686	H1-hESC	embryonic stem cell:	n/a	n/a
42	HA-E2F1	chr4:95678701-95680381	MCF-7	breast:	n/a	chr4:95679542-95679552 chr4:95679544-95679553 chr4:95680197-95680204 chr4:95679618-95679630 chr4:95679539-95679549
43	HDAC2	chr4:95678784-95679082	H1-hESC	embryonic stem cell:	n/a	chr4:95678991-95679005 chr4:95678992-95679006
44	JUN	chr4:95679401-95679411	H1-hESC	embryonic stem cell:	n/a	n/a
45	JUND	chr4:95679784-95680004	H1-hESC	embryonic stem cell:	n/a	n/a
46	JUND	chr4:95679417-95679596	H1-hESC	embryonic stem cell:	n/a	chr4:95679547-95679556
47	MAX	chr4:95679452-95679713	H1-hESC	embryonic stem cell:	n/a	chr4:95679555-95679566 chr4:95679555-95679566 chr4:95679555-95679565 chr4:95679554-95679567
48	MAX	chr4:95679330-95679839	MCF-7	breast:	n/a	chr4:95679555-95679566 chr4:95679555-95679566 chr4:95679555-95679565 chr4:95679554-95679567
49	MAX	chr4:95679346-95680179	A549	lung:	n/a	chr4:95679555-95679566 chr4:95679555-95679566 chr4:95679555-95679565 chr4:95679554-95679567
50	MAX	chr4:95678600-95680454	A549	lung:	n/a	chr4:95679555-95679566 chr4:95679555-95679566 chr4:95679555-95679565 chr4:95679554-95679567

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:95679381-95679431	HCM	heart:	n/a
2	chr4:95679381-95679431	HCM	heart:	n/a
3	chr4:95679381-95679431	HUVEC	blood vessel:	n/a
4	chr4:95679381-95679431	CMK	blood:	n/a
5	chr4:95679381-95679431	PFSK-1	brain:	n/a
6	chr4:95679381-95679431	ECC-1	luminal epithelium:	n/a
7	chr4:95679381-95679431	AG04450	lung:	fetal
8	chr4:95679705-95679755	CMK	blood:	n/a
9	chr4:95679705-95679755	SK-N-MC	brain:	n/a
10	chr4:95679381-95679431	Caco-2	colon:	n/a
11	chr4:95679705-95679755	MCF10A-Er-Src	breast:	n/a
12	chr4:95679705-95679755	SK-N-SH_RA	brain:	n/a
13	chr4:95679381-95679431	HNPCEpiC	eye:	n/a
14	chr4:95679381-95679431	IMR90	lung:	fetal
15	chr4:95679705-95679755	MCF-7	breast:	n/a
16	chr4:95679381-95679431	HCPEpiC	choroid plexus:	n/a
17	chr4:95679705-95679755	HepG2	liver:	n/a
18	chr4:95679381-95679431	HRE	kidney:	n/a
19	chr4:95679381-95679431	GM19239	blood:	n/a
20	chr4:95679381-95679431	T-47D	breast:	n/a
21	chr4:95679381-95679431	NH-A	brain:	n/a
22	chr4:95679705-95679755	SAEC	small airway:	n/a
23	chr4:95679705-95679755	AG09309	skin:	n/a
24	chr4:95679705-95679755	GM19239	blood:	n/a
25	chr4:95679705-95679755	IMR90	lung:	fetal
26	chr4:95679381-95679431	SKMC	muscle:	n/a
27	chr4:95679381-95679431	HCT-116	colon:	n/a
28	chr4:95679705-95679755	K562	blood:	n/a
29	chr4:95679705-95679755	RPTEC	kidney:	n/a
30	chr4:95679381-95679431	H1-hESC	embryonic stem cell:	embryo
31	chr4:95679381-95679431	GM06990	blood:	n/a
32	chr4:95679381-95679431	GM12892	blood:	n/a
33	chr4:95679381-95679431	GM12878	blood:	n/a
34	chr4:95679705-95679755	Hela-S3	cervix:	n/a
35	chr4:95679705-95679755	NHBE	bronchial:	n/a
36	chr4:95679381-95679431	RPTEC	kidney:	n/a
37	chr4:95679705-95679755	NB4	blood:	n/a
38	chr4:95679381-95679431	PrEC	prostate:	n/a
39	chr4:95679381-95679431	NT2-D1	testis:	n/a
40	chr4:95679705-95679755	Caco-2	colon:	n/a
41	chr4:95679705-95679755	Hepatocyte	liver:	n/a
42	chr4:95679381-95679431	HEEpiC	esophagus:	n/a
43	chr4:95679381-95679431	A549	lung:	n/a
44	chr4:95679705-95679755	HEEpiC	esophagus:	n/a
45	chr4:95679705-95679755	HNPCEpiC	eye:	n/a
46	chr4:95679705-95679755	HCPEpiC	choroid plexus:	n/a
47	chr4:95679381-95679431	AG09319	gingival:	n/a
48	chr4:95679705-95679755	HUVEC	blood vessel:	n/a
49	chr4:95679705-95679755	LNCaP	prostate:	n/a
50	chr4:95679705-95679755	SK-N-SH	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr4:95678678..95680883-chr4:96023985..96026151,2	MCF-7	breast:
2	chr4:95679187..95680719-chr4:95971290..95974263,2	MCF-7	breast:
3	chr4:95679588..95681847-chr4:96013272..96015095,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-UNC5C-1	chr4:95678545-95679036	NONHSAT097457

Variant related genes	Relation type
ENSG00000249599	TF binding region
BMPR1B	TF binding region
ENSG00000249599	CpG island
BMPR1B	CpG island
ENSG00000138696	chromatin interactions

Extended variants
information (count: 18 )
Associated
traits (count: 81 )

Variant overlapped rSNPs/rCNVs (count:18 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs374976274	chr4:95679070-95679071	Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs544163908	chr4:95679078-95679079	Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs202068629	chr4:95679090-95679091	Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs563992994	chr4:95679173-95679174	Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs149673144	chr4:95679320-95679321	Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs546427396	chr4:95679423-95679424	Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs370399814	chr4:95679488-95679489	Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs559679402	chr4:95679489-95679490	Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs539479910	chr4:95679570-95679571	Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs111448434	chr4:95679602-95679603	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs143954594	chr4:95679622-95679623	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs368638988	chr4:95679631-95679632	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs561757048	chr4:95679639-95679640	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs533112035	chr4:95679673-95679674	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs369543484	chr4:95679677-95679678	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs530439687	chr4:95679722-95679723	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs77862780	chr4:95679754-95679755	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs572921596	chr4:95679773-95679774	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:81)

Disease	PMID	Source
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Medulloblastoma	21979893	CNVD
Neuroblastoma	18923191	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21858162	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
lymphocytic leukemia	21291569	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	17603634	CNVD
Hepatocellular carcinoma	16750200	CNVD
Myxofibrosarcoma	16751306	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Parkinson disease	18923514	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Cancer	21183584	CNVD
Breast cancer	16272173	CNVD
Colorectal cancer	19359472	CNVD
Malignant mesothelioma	18160781	CNVD
Medulloblastoma	18056178	CNVD
Multiple myeloma	17077331	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Oral squamous cell carcinoma	17134496	CNVD
4q-syndrome	17576883	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Muscular dystrophy	21149563	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Cervical cancer	21062161	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	16608533	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Lung cancer	19208797	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21785460	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Myelodysplastic syndrome	21251322	CNVD
Lung cancer	18438408	CNVD
Cancer	22429812	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	18414403	CNVD
primary effusion lymphomas	17116491	CNVD
Mental retardation	20522426	CNVD
delayed speech	20522426	CNVD
growth disorder	20522426	CNVD
small cell lung cancer	20016488	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17133270	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Colorectal cancer	20459617	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Hirschsprung''s Disease	21712996	CNVD
Congenital anomalies of the kidney and urinary tract	20505237	CNVD
Breast cancer	17393978	CNVD
Ovarian cancer	21720365	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Esophageal cancer	21851588	CNVD
Cancer	19907438	CNVD
Prostate cancer	16573809	CNVD
Multiple myeloma	16616336	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:133 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:95677800-95681800	Active TSS	A549	lung
2	chr4:95678000-95680000	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
3	chr4:95678000-95680200	Active TSS	NH-A	brain
4	chr4:95678000-95682000	Active TSS	Stomach Smooth Muscle	stomach
5	chr4:95678200-95679600	Bivalent/Poised TSS	Brain Germinal Matrix	brain
6	chr4:95678200-95680000	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr4:95678200-95680400	Active TSS	Aorta	Aorta
8	chr4:95678200-95680400	Bivalent/Poised TSS	Rectal Smooth Muscle	rectum
9	chr4:95678200-95680400	Active TSS	HMEC	breast
10	chr4:95678400-95679400	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
11	chr4:95678400-95679600	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin01	Skin
12	chr4:95678400-95679600	Bivalent/Poised TSS	Foreskin Melanocyte Primary Cells skin03	Skin
13	chr4:95678400-95679600	Active TSS	Fetal Brain Female	brain
14	chr4:95678400-95679800	Bivalent/Poised TSS	IMR90 fetal lung fibroblasts Cell Line	lung
15	chr4:95678400-95679800	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
16	chr4:95678400-95680000	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
17	chr4:95678400-95680000	Bivalent/Poised TSS	Thymus	Thymus
18	chr4:95678400-95680200	Bivalent/Poised TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
19	chr4:95678400-95680200	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
20	chr4:95678400-95680400	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
21	chr4:95678400-95680600	Bivalent/Poised TSS	H1 Cell Line	embryonic stem cell
22	chr4:95678400-95680600	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
23	chr4:95678400-95680600	Active TSS	Ovary	ovary
24	chr4:95678400-95680800	Bivalent/Poised TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
25	chr4:95678400-95680800	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
26	chr4:95678600-95679200	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
27	chr4:95678600-95679200	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Female	--
28	chr4:95678600-95679600	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
29	chr4:95678600-95679600	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
30	chr4:95678600-95679600	Bivalent/Poised TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
31	chr4:95678600-95679600	Bivalent/Poised TSS	Duodenum Mucosa	Duodenum
32	chr4:95678600-95679600	Active TSS	Fetal Kidney	kidney
33	chr4:95678600-95679600	Active TSS	Right Atrium	heart
34	chr4:95678600-95679800	Active TSS	Brain Angular Gyrus	brain
35	chr4:95678600-95679800	Bivalent/Poised TSS	Rectal Mucosa Donor 31	rectum
36	chr4:95678600-95680000	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
37	chr4:95678600-95680000	Active TSS	Pancreatic Islets	Pancreatic Islet
38	chr4:95678600-95680000	Bivalent/Poised TSS	Left Ventricle	heart
39	chr4:95678600-95680200	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
40	chr4:95678600-95680200	Active TSS	Breast Myoepithelial Primary Cells	Breast
41	chr4:95678600-95680200	Bivalent/Poised TSS	Skeletal Muscle Male	skeletal muscle
42	chr4:95678600-95680400	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
43	chr4:95678600-95680400	Bivalent/Poised TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
44	chr4:95678600-95680400	Bivalent/Poised TSS	iPS DF 6.9 Cell Line	embryonic stem cell
45	chr4:95678600-95680400	Bivalent/Poised TSS	Primary T cells from cord blood	blood
46	chr4:95678600-95680400	Active TSS	Brain Substantia Nigra	brain
47	chr4:95678600-95680400	Bivalent/Poised TSS	Fetal Stomach	stomach
48	chr4:95678600-95680400	Active TSS	Pancreas	Pancrea
49	chr4:95678600-95680600	Active TSS	Brain Anterior Caudate	brain
50	chr4:95678600-95680600	Active TSS	Brain Inferior Temporal Lobe	brain

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