Variant report

Variant	nsv913422
Chromosome Location	chr21:17791751-17826260
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	BRCA1	chr21:17791560-17792044	Hela-S3	cervix:	n/a	n/a
2	CCNT2	chr21:17793344-17793475	K562	blood:	n/a	n/a
3	CEBPB	chr21:17796273-17796481	Hela-S3	cervix:	n/a	chr21:17796368-17796379 chr21:17796366-17796379
4	CEBPB	chr21:17818801-17819060	HepG2	liver:	n/a	chr21:17818924-17818935
5	CEBPB	chr21:17794875-17795400	Hela-S3	cervix:	n/a	chr21:17794990-17795001 chr21:17794990-17795003
6	CEBPB	chr21:17797768-17798408	Hela-S3	cervix:	n/a	n/a
7	CEBPB	chr21:17792367-17792742	ECC-1	luminal epithelium:	n/a	chr21:17792377-17792386
8	CEBPB	chr21:17792425-17792909	Hela-S3	cervix:	n/a	n/a
9	CHD2	chr21:17791479-17792210	Hela-S3	cervix:	n/a	n/a
10	CTCF	chr21:17800537-17800627	Kidney_OC	kidney:	n/a	n/a
11	E2F4	chr21:17792581-17792835	MCF10A-Er-Src	breast:	n/a	n/a
12	E2F4	chr21:17799768-17799938	MCF10A-Er-Src	breast:	n/a	n/a
13	ELF1	chr21:17791233-17791845	MCF-7	breast:	n/a	n/a
14	EP300	chr21:17797663-17798260	Hela-S3	cervix:	n/a	n/a
15	EP300	chr21:17797155-17799919	SK-N-SH	brain:	n/a	chr21:17797369-17797378
16	EP300	chr21:17826072-17826076	GM12878	blood:	n/a	n/a
17	EP300	chr21:17798156-17798429	SK-N-SH_RA	brain:	n/a	n/a
18	EP300	chr21:17791466-17791843	SK-N-SH_RA	brain:	n/a	chr21:17791596-17791606
19	EP300	chr21:17799814-17800446	ECC-1	luminal epithelium:	n/a	chr21:17799971-17799985 chr21:17799978-17799992 chr21:17799968-17799982 chr21:17799970-17799984 chr21:17799969-17799983 chr21:17799972-17799986
20	EP300	chr21:17792320-17792861	Hela-S3	cervix:	n/a	n/a
21	EP300	chr21:17792447-17792711	SK-N-SH_RA	brain:	n/a	n/a
22	EP300	chr21:17792345-17792885	ECC-1	luminal epithelium:	n/a	n/a
23	EP300	chr21:17791394-17791805	SK-N-SH_RA	brain:	n/a	chr21:17791596-17791606
24	EP300	chr21:17792230-17793023	ECC-1	luminal epithelium:	n/a	n/a
25	ESR1	chr21:17792349-17792958	ECC-1	luminal epithelium:	n/a	chr21:17792723-17792740
26	ESR1	chr21:17803418-17803879	ECC-1	luminal epithelium:	n/a	n/a
27	ESR1	chr21:17803396-17803834	ECC-1	luminal epithelium:	n/a	n/a
28	ESR1	chr21:17800643-17801437	ECC-1	luminal epithelium:	n/a	chr21:17800982-17800999 chr21:17800983-17801000
29	ESR1	chr21:17803565-17803786	ECC-1	luminal epithelium:	n/a	n/a
30	ESR1	chr21:17792410-17792831	ECC-1	luminal epithelium:	n/a	chr21:17792723-17792740
31	ESR1	chr21:17800801-17801392	ECC-1	luminal epithelium:	n/a	chr21:17800982-17800999 chr21:17800983-17801000
32	ESR1	chr21:17800843-17801192	ECC-1	luminal epithelium:	n/a	chr21:17800982-17800999 chr21:17800983-17801000
33	ESR1	chr21:17800738-17801435	ECC-1	luminal epithelium:	n/a	chr21:17800982-17800999 chr21:17800983-17801000
34	ESR1	chr21:17803443-17803867	ECC-1	luminal epithelium:	n/a	n/a
35	ESR1	chr21:17800724-17801392	ECC-1	luminal epithelium:	n/a	chr21:17800982-17800999 chr21:17800983-17801000
36	ESR1	chr21:17792414-17792864	ECC-1	luminal epithelium:	n/a	chr21:17792723-17792740
37	FOS	chr21:17797602-17798217	HUVEC	blood vessel:	n/a	n/a
38	FOS	chr21:17818869-17819045	MCF10A-Er-Src	breast:	n/a	n/a
39	FOS	chr21:17818346-17818635	MCF10A-Er-Src	breast:	n/a	n/a
40	FOS	chr21:17818869-17819102	MCF10A-Er-Src	breast:	n/a	n/a
41	FOS	chr21:17798152-17798305	MCF10A-Er-Src	breast:	n/a	n/a
42	FOS	chr21:17818346-17818632	MCF10A-Er-Src	breast:	n/a	n/a
43	FOS	chr21:17818346-17818656	MCF10A-Er-Src	breast:	n/a	n/a
44	FOS	chr21:17798165-17798330	MCF10A-Er-Src	breast:	n/a	n/a
45	FOS	chr21:17796729-17797285	HUVEC	blood vessel:	n/a	chr21:17797059-17797069
46	FOXA1	chr21:17792445-17792710	T-47D	breast:	n/a	n/a
47	FOXA1	chr21:17791426-17791756	T-47D	breast:	n/a	chr21:17791447-17791459
48	FOXA1	chr21:17792406-17792815	T-47D	breast:	n/a	n/a
49	FOXA1	chr21:17792433-17792758	HepG2	liver:	n/a	n/a
50	FOXA1	chr21:17792438-17792848	ECC-1	luminal epithelium:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr21:17795082..17798298-chr21:17801061..17804757,3	MCF-7	breast:
2	chr21:17802778..17805125-chr21:17808909..17810799,2	MCF-7	breast:
3	chr21:17812930..17814449-chr21:17824658..17826257,2	MCF-7	breast:
4	chr21:17793428..17795619-chr21:17796309..17799030,2	MCF-7	breast:
5	chr21:17795082..17798298-chr21:17801061..17804757,3	MCF-7	breast:
6	chr21:17793428..17795619-chr21:17796309..17799030,2	MCF-7	breast:
7	chr21:17812930..17814449-chr21:17824658..17826257,2	MCF-7	breast:
8	chr21:17789969..17792696-chr21:17799605..17801790,2	MCF-7	breast:
9	chr21:17802778..17805125-chr21:17808909..17810799,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-USP25-2	chr21:17791999-17792061	ENSG00000215386
2	lnc-USP25-2	chr21:17791716-17792061	NONHSAT081235
3	lnc-USP25-2	chr21:17791752-17792061	ENSG00000215386
4	lnc-USP25-2	chr21:17791722-17792061	ENSG00000215386.6
5	lnc-USP25-2	chr21:17791593-17792061	XLOC_013868
6	lnc-USP25-2	chr21:17791648-17792061	ENSG00000215386.6
7	lnc-USP25-2	chr21:17792775-17792892	ENSG00000215386.6
8	lnc-USP25-2	chr21:17791838-17792061	ENSG00000215386

Variant related genes	Relation type
ENSG00000270139	TF binding region
LINC00478	TF binding region
ENSG00000215386	chromatin interactions
ENSG00000270139	chromatin interactions
RNF145	miRNA target sites
COX7A2L	miRNA target sites
CAMTA1	miRNA target sites

Extended variants
information (count: 1417 )
Associated
traits (count: 72 )

Variant overlapped rSNPs/rCNVs (count:1417 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs3737408	chr21:17791751-17791752	Enhancers Active TSS Flanking Active TSS	TF binding region lncRNA	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs61441283	chr21:17791770-17791771	Enhancers Active TSS Flanking Active TSS	TF binding region lncRNA	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs150994926	chr21:17791801-17791802	Enhancers Flanking Active TSS Active TSS	TF binding region lncRNA	2 gene(s)	Overlapped CNVs	n/a
4	rs58524891	chr21:17791809-17791810	Enhancers Flanking Active TSS Active TSS	TF binding region lncRNA	2 gene(s)	Overlapped CNVs	n/a
5	rs397774381	chr21:17791822-17791823	Enhancers Flanking Active TSS Active TSS	TF binding region lncRNA	2 gene(s)	Overlapped CNVs	n/a
6	rs240452	chr21:17791840-17791841	Enhancers Flanking Active TSS Active TSS	TF binding region lncRNA	2 gene(s)	Overlapped CNVs	n/a
7	rs240451	chr21:17791847-17791848	Enhancers Flanking Active TSS Active TSS	TF binding region lncRNA	2 gene(s)	Overlapped CNVs	n/a
8	rs140862771	chr21:17791915-17791916	Enhancers Flanking Active TSS Active TSS	TF binding region lncRNA	2 gene(s)	Overlapped CNVs	n/a
9	rs149750570	chr21:17791954-17791955	Enhancers Flanking Active TSS Active TSS	TF binding region lncRNA	2 gene(s)	Overlapped CNVs	n/a
10	rs79131195	chr21:17792020-17792021	Enhancers Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region lncRNA	2 gene(s)	Overlapped CNVs	n/a
11	rs191158415	chr21:17792031-17792032	Enhancers Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region lncRNA	2 gene(s)	Overlapped CNVs	n/a
12	rs552674379	chr21:17792137-17792138	Enhancers Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region	2 gene(s)	Overlapped CNVs	n/a
13	rs558673335	chr21:17792144-17792145	Enhancers Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region	2 gene(s)	Overlapped CNVs	n/a
14	rs578132900	chr21:17792160-17792161	Enhancers Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region	2 gene(s)	Overlapped CNVs	n/a
15	rs575076896	chr21:17792162-17792163	Enhancers Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region	2 gene(s)	Overlapped CNVs	n/a
16	rs371451026	chr21:17792212-17792213	Enhancers Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region	2 gene(s)	Overlapped CNVs	n/a
17	rs9977021	chr21:17792239-17792240	Enhancers Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs560641535	chr21:17792275-17792276	Enhancers Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region	2 gene(s)	Overlapped CNVs	n/a
19	rs574239342	chr21:17792302-17792303	Enhancers Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region	2 gene(s)	Overlapped CNVs	n/a
20	rs183120804	chr21:17792347-17792348	Enhancers Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region	2 gene(s)	Overlapped CNVs	n/a
21	rs562495072	chr21:17792404-17792405	Enhancers Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region	2 gene(s)	Overlapped CNVs	n/a
22	rs117716045	chr21:17792567-17792568	Enhancers Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region	2 gene(s)	Overlapped CNVs	n/a
23	rs565018068	chr21:17792575-17792576	Enhancers Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region	2 gene(s)	Overlapped CNVs	n/a
24	rs186024489	chr21:17792590-17792591	Enhancers Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region	2 gene(s)	Overlapped CNVs	n/a
25	rs371482628	chr21:17792660-17792661	Enhancers Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region	2 gene(s)	Overlapped CNVs	n/a
26	rs34336169	chr21:17792661-17792662	Enhancers Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region	2 gene(s)	Overlapped CNVs	n/a
27	rs376588628	chr21:17792677-17792678	Enhancers Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region	2 gene(s)	Overlapped CNVs	n/a
28	rs527516591	chr21:17792746-17792747	Enhancers Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region	2 gene(s)	Overlapped CNVs	n/a
29	rs190494648	chr21:17792830-17792831	Enhancers Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
30	rs567460209	chr21:17792857-17792858	Enhancers Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
31	rs146654061	chr21:17792884-17792885	Enhancers Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
32	rs550099451	chr21:17792891-17792892	Enhancers Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
33	rs569710986	chr21:17792908-17792909	Enhancers Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs538620383	chr21:17792911-17792912	Enhancers Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs140225006	chr21:17792918-17792919	Enhancers Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs528507470	chr21:17792964-17792965	Enhancers Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs561760249	chr21:17793034-17793035	Flanking Active TSS Active TSS Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs548555638	chr21:17793036-17793037	Flanking Active TSS Active TSS Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs572077209	chr21:17793050-17793051	Flanking Active TSS Active TSS Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs527326533	chr21:17793073-17793074	Flanking Active TSS Active TSS Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs534142753	chr21:17793115-17793116	Flanking Active TSS Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs183463843	chr21:17793129-17793130	Flanking Active TSS Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs574253885	chr21:17793180-17793181	Flanking Active TSS Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs542960424	chr21:17793196-17793197	Flanking Active TSS Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs547041158	chr21:17793263-17793264	Flanking Active TSS Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs187695477	chr21:17793280-17793281	Flanking Active TSS Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs75142640	chr21:17793407-17793408	Flanking Active TSS Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs544973976	chr21:17793421-17793422	Flanking Active TSS Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs565251525	chr21:17793428-17793429	Flanking Active TSS Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs192726251	chr21:17793432-17793433	Flanking Active TSS Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:72)

Disease	PMID	Source
Ovarian cancer	21720365	CNVD
Wilms tumour	21544195	CNVD
Esophageal cancer	21851588	CNVD
Glioblastoma multiforme	21080181	CNVD
Cancer	16751803	CNVD
Medulloblastoma	21979893	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Down syndrome	17412756	CNVD
Down syndrome	17576883	CNVD
Acute promyelocytic leukemia	19109227	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	20729466	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell lymphomas	19863542	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	17387387	CNVD
Renal cell carcinoma	19461508	CNVD
Seminomas	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Metanephric adenoma	20802469	CNVD
Neuroblastoma	18923191	CNVD
Prostate cancer	19156837	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Cancer	20164919	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
lymphocytic leukemia	21291569	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Acute myeloid leukemia	21251322	CNVD
abnormal development	18461090	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21364760	CNVD
Multiple myeloma	17550852	CNVD
Myelofibrosis	22110671	CNVD
Alzheimer''s disease	18923514	CNVD
Alzheimer''s disease	20877625	CNVD
Follicular lymphoma	20505157	CNVD
Alzheimer''s disease	21956041	CNVD
Cancer	21183584	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Melanoma	18172304	CNVD
Autism	22958593	CNVD
Schizophrenia	22958593	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Epilepsy	20502679	CNVD
22q11.2 microdeletion syndrome	19750312	CNVD
Breast cancer	20409316	CNVD
Gastric cancer	18160780	CNVD
Medullary thyroid carcinoma	18765511	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Pancreatic cancer	17952125	CNVD
T-cell lymphomas	22341440	CNVD

Chromatin state (count:378 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:17790400-17792400	Flanking Active TSS	Osteobl	bone
2	chr21:17790400-17793000	Active TSS	Psoas Muscle	Psoas
3	chr21:17790400-17797000	Active TSS	Skeletal Muscle Female	skeletal muscle
4	chr21:17790600-17793000	Active TSS	Right Ventricle	heart
5	chr21:17790600-17793200	Active TSS	Right Atrium	heart
6	chr21:17790800-17791800	Flanking Active TSS	Adipose Nuclei	Adipose
7	chr21:17790800-17793000	Active TSS	NHDF-Ad	bronchial
8	chr21:17791000-17791800	Enhancers	HUES6 Cell Line	embryonic stem cell
9	chr21:17791000-17791800	Enhancers	NHEK	skin
10	chr21:17791000-17793000	Enhancers	Stomach Mucosa	stomach
11	chr21:17791200-17792000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
12	chr21:17791200-17795200	Active TSS	A549	lung
13	chr21:17791200-17797000	Active TSS	Fetal Brain Female	brain
14	chr21:17791400-17791800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
15	chr21:17791400-17791800	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
16	chr21:17791400-17791800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
17	chr21:17791400-17791800	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
18	chr21:17791400-17791800	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
19	chr21:17791400-17791800	Flanking Active TSS	Brain Anterior Caudate	brain
20	chr21:17791400-17791800	Flanking Active TSS	Fetal Lung	lung
21	chr21:17791400-17792600	Active TSS	Esophagus	oesophagus
22	chr21:17791400-17792800	Active TSS	Brain Substantia Nigra	brain
23	chr21:17791400-17792800	Active TSS	Left Ventricle	heart
24	chr21:17791400-17793000	Flanking Active TSS	Muscle Satellite Cultured Cells	--
25	chr21:17791400-17793000	Active TSS	Fetal Muscle Trunk	muscle
26	chr21:17791400-17793000	Active TSS	Ovary	ovary
27	chr21:17791400-17793000	Active TSS	Rectal Smooth Muscle	rectum
28	chr21:17791400-17793400	Active TSS	Brain Angular Gyrus	brain
29	chr21:17791400-17793600	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
30	chr21:17791400-17793600	Active TSS	Duodenum Smooth Muscle	Duodenum
31	chr21:17791400-17793800	Active TSS	Brain Cingulate Gyrus	brain
32	chr21:17791400-17795000	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
33	chr21:17791400-17795200	Active TSS	Pancreatic Islets	Pancreatic Islet
34	chr21:17791400-17795400	Active TSS	Brain Hippocampus Middle	brain
35	chr21:17791400-17795600	Active TSS	Brain Germinal Matrix	brain
36	chr21:17791400-17796800	Active TSS	Skeletal Muscle Male	skeletal muscle
37	chr21:17791400-17797000	Active TSS	Stomach Smooth Muscle	stomach
38	chr21:17791400-17797200	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
39	chr21:17791400-17797200	Active TSS	Breast Myoepithelial Primary Cells	Breast
40	chr21:17791600-17791800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
41	chr21:17791600-17791800	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
42	chr21:17791600-17791800	Flanking Active TSS	HSMM	muscle
43	chr21:17791600-17792000	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
44	chr21:17791600-17792000	Active TSS	Fetal Kidney	kidney
45	chr21:17791600-17792400	Active TSS	Rectal Mucosa Donor 29	rectum
46	chr21:17791600-17792600	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
47	chr21:17791600-17793000	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
48	chr21:17791600-17793000	Active TSS	Aorta	Aorta
49	chr21:17791600-17793200	Active TSS	Fetal Adrenal Gland	Adrenal Gland
50	chr21:17791600-17793200	Active TSS	Hela-S3	cervix

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