Variant report

Variant	nsv979524
Chromosome Location	chr21:15431964-15441809
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:93)
CpG islands
(count:428)
Chromatin interactive
region (count:0)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:93 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CEBPB	chr21:15434082-15434240	A549	lung:	n/a	n/a
2	CEBPB	chr21:15434091-15434297	IMR90	lung:	n/a	n/a
3	CEBPB	chr21:15434434-15434634	HepG2	liver:	n/a	n/a
4	CTCF	chr21:15434007-15434042	Lung_OC	lung:	n/a	n/a
5	CTCF	chr21:15435972-15436005	H1-hESC	embryonic stem cell:	n/a	n/a
6	CTCF	chr21:15440987-15440998	GM10266	blood:	n/a	n/a
7	CTCF	chr21:15435964-15436158	GM19238	blood:	n/a	n/a
8	CTCF	chr21:15436040-15436190	GM12867	blood:	n/a	n/a
9	CTCF	chr21:15436280-15436284	MCF-7	breast:	n/a	n/a
10	CTCF	chr21:15436665-15436862	MCF-7	breast:	n/a	n/a
11	CTCF	chr21:15436244-15436319	MCF-7	breast:	n/a	chr21:15436278-15436291
12	CTCF	chr21:15436675-15436862	MCF-7	breast:	n/a	n/a
13	CTCF	chr21:15435937-15436126	A549	lung:	n/a	n/a
14	CTCF	chr21:15435884-15436277	MCF-7	breast:	n/a	n/a
15	CTCF	chr21:15435855-15436216	A549	lung:	n/a	n/a
16	CTCF	chr21:15435509-15435553	GM13976	blood:	n/a	n/a
17	CTCF	chr21:15432498-15432500	GM12891	blood:	n/a	n/a
18	CTCF	chr21:15435862-15436154	A549	lung:	n/a	n/a
19	CTCF	chr21:15435861-15436321	MCF-7	breast:	n/a	chr21:15436278-15436291
20	CTCF	chr21:15436696-15436823	MCF-7	breast:	n/a	n/a
21	CTCF	chr21:15436660-15436810	MCF-7	breast:	n/a	n/a
22	CTCF	chr21:15436053-15436093	GM12891	blood:	n/a	n/a
23	CTCF	chr21:15435900-15436134	MCF-7	breast:	n/a	n/a
24	CTCF	chr21:15435938-15436080	SK-N-SH_RA	brain:	n/a	n/a
25	CTCF	chr21:15435871-15436360	MCF-7	breast:	n/a	chr21:15436278-15436291
26	CTCF	chr21:15435890-15436167	MCF-7	breast:	n/a	n/a
27	CTCF	chr21:15436665-15436833	MCF-7	breast:	n/a	n/a
28	CTCF	chr21:15435980-15436130	AG09319	gingival:	n/a	n/a
29	CTCF	chr21:15436100-15436250	GM12870	blood:	n/a	n/a
30	CTCF	chr21:15436620-15436770	GM12873	blood:	n/a	n/a
31	CTCF	chr21:15431913-15431972	LNCaP	prostate:	n/a	chr21:15431952-15431970
32	CTCF	chr21:15436720-15436870	SK-N-SH_RA	brain:	n/a	n/a
33	CTCF	chr21:15431858-15432007	MCF-7	breast:	n/a	chr21:15431952-15431970
34	CTCF	chr21:15436160-15436310	GM12864	blood:	n/a	chr21:15436278-15436291
35	CTCF	chr21:15432453-15432497	GM12891	blood:	n/a	n/a
36	CTCF	chr21:15436669-15436861	MCF-7	breast:	n/a	n/a
37	CTCF	chr21:15431854-15432037	MCF-7	breast:	n/a	chr21:15431952-15431970
38	CTCF	chr21:15435975-15436134	A549	lung:	n/a	n/a
39	CTCF	chr21:15431847-15432024	MCF-7	breast:	n/a	chr21:15431952-15431970
40	CTCF	chr21:15435918-15436153	ProgFib	skin:	n/a	n/a
41	CTCF	chr21:15436000-15436150	SK-N-SH_RA	brain:	n/a	n/a
42	CTCF	chr21:15436680-15436830	NHDF-neo	bronchial:	n/a	n/a
43	CTCF	chr21:15431863-15432018	MCF-7	breast:	n/a	chr21:15431952-15431970
44	CTCF	chr21:15436719-15436772	ProgFib	skin:	n/a	n/a
45	CTCF	chr21:15436160-15436310	GM12871	blood:	n/a	chr21:15436278-15436291
46	CTCF	chr21:15436620-15436770	AG09319	gingival:	n/a	n/a
47	CTCF	chr21:15431854-15432028	MCF-7	breast:	n/a	chr21:15431952-15431970
48	CTCF	chr21:15435997-15436180	IMR90	lung:	n/a	n/a
49	ELF1	chr21:15435975-15436884	MCF-7	breast:	n/a	chr21:15436326-15436335 chr21:15436858-15436870 chr21:15436560-15436572 chr21:15436325-15436336 chr21:15436339-15436351
50	ELF1	chr21:15436528-15436820	SK-N-SH	brain:	n/a	chr21:15436560-15436572

(count:428 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr21:15436866-15436916	MCF-7	breast:	n/a
2	chr21:15436866-15436916	MCF-7	breast:	n/a
3	chr21:15436260-15436310	GM06990	blood:	n/a
4	chr21:15436866-15436916	MCF10A-Er-Src	breast:	n/a
5	chr21:15437169-15437219	HCF	heart:	n/a
6	chr21:15432857-15432907	H1-hESC	embryonic stem cell:	embryo
7	chr21:15435310-15435360	SK-N-SH_RA	brain:	n/a
8	chr21:15437169-15437219	AG04450	lung:	fetal
9	chr21:15434350-15434400	Hepatocyte	liver:	n/a
10	chr21:15434350-15434400	AG10803	skin:	n/a
11	chr21:15434350-15434400	HRE	kidney:	n/a
12	chr21:15435310-15435360	HMEC	breast:	n/a
13	chr21:15434350-15434400	AG04449	skin:	fetal
14	chr21:15435310-15435360	HepG2	liver:	n/a
15	chr21:15436866-15436916	HCF	heart:	n/a
16	chr21:15436260-15436310	HRE	kidney:	n/a
17	chr21:15436866-15436916	A549	lung:	n/a
18	chr21:15436260-15436310	IMR90	lung:	fetal
19	chr21:15434350-15434400	HNPCEpiC	eye:	n/a
20	chr21:15435310-15435360	NT2-D1	testis:	n/a
21	chr21:15436419-15436469	BJ	skin:	n/a
22	chr21:15434350-15434400	HCT-116	colon:	n/a
23	chr21:15435310-15435360	SKMC	muscle:	n/a
24	chr21:15435310-15435360	HCPEpiC	choroid plexus:	n/a
25	chr21:15437169-15437219	SK-N-SH_RA	brain:	n/a
26	chr21:15436866-15436916	GM12878	blood:	n/a
27	chr21:15436260-15436310	HRCEpiC	kidney:	n/a
28	chr21:15436866-15436916	HUVEC	blood vessel:	n/a
29	chr21:15436866-15436916	HCPEpiC	choroid plexus:	n/a
30	chr21:15436866-15436916	AoSMC	blood vessel:	n/a
31	chr21:15432857-15432907	AG09309	skin:	n/a
32	chr21:15437169-15437219	HepG2	liver:	n/a
33	chr21:15432857-15432907	HCM	heart:	n/a
34	chr21:15436419-15436469	PFSK-1	brain:	n/a
35	chr21:15437169-15437219	HMEC	breast:	n/a
36	chr21:15436866-15436916	CMK	blood:	n/a
37	chr21:15436260-15436310	A549	lung:	n/a
38	chr21:15436419-15436469	Jurkat	blood:	n/a
39	chr21:15436866-15436916	HEEpiC	esophagus:	n/a
40	chr21:15436419-15436469	AG04450	lung:	fetal
41	chr21:15434350-15434400	HEEpiC	esophagus:	n/a
42	chr21:15436260-15436310	GM12892	blood:	n/a
43	chr21:15432857-15432907	BJ	skin:	n/a
44	chr21:15436866-15436916	GM06990	blood:	n/a
45	chr21:15432857-15432907	NHDF-neo	bronchial:	n/a
46	chr21:15436419-15436469	HEK293	kidney:	embryo
47	chr21:15436866-15436916	NHBE	bronchial:	n/a
48	chr21:15434350-15434400	IMR90	lung:	fetal
49	chr21:15436260-15436310	BE2_C	brain:	n/a
50	chr21:15436260-15436310	T-47D	breast:	n/a

No data

Variant related genes	Relation type
RNA5SP488	TF binding region
ANKRD20A18P	TF binding region
RNA5SP488	CpG island
ANKRD20A18P	CpG island

Extended variants
information (count: 736 )
Associated
traits (count: 60 )

Variant overlapped rSNPs/rCNVs (count:736 , 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	rs368518167	chr21:15432001-15432002	Weak transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs558302417	chr21:15432097-15432098	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
3	rs528224133	chr21:15432101-15432102	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
4	rs201367651	chr21:15432148-15432149	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
5	rs76159057	chr21:15432199-15432200	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
6	rs79202232	chr21:15432228-15432229	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
7	rs561708797	chr21:15432237-15432238	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
8	rs375111626	chr21:15432252-15432253	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
9	rs369542178	chr21:15432253-15432254	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
10	rs571135599	chr21:15432266-15432267	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
11	rs372527549	chr21:15432292-15432293	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
12	rs200624059	chr21:15432311-15432312	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
13	rs369572033	chr21:15432316-15432317	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
14	rs373038362	chr21:15432339-15432340	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
15	rs111715837	chr21:15432356-15432357	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
16	rs111987918	chr21:15432552-15432553	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
17	rs569561378	chr21:15432562-15432563	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
18	rs71182501	chr21:15432571-15432572	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
19	rs547190902	chr21:15432599-15432600	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
20	rs566601905	chr21:15432618-15432619	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs13051997	chr21:15432620-15432621	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs535585709	chr21:15432636-15432637	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs184532572	chr21:15432646-15432647	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs568955628	chr21:15432647-15432648	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs1810863	chr21:15432657-15432658	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs543276002	chr21:15432686-15432687	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs199536049	chr21:15432711-15432712	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs556935206	chr21:15432712-15432713	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs140359394	chr21:15432716-15432717	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs545657643	chr21:15432723-15432724	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs71330026	chr21:15432736-15432737	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs369821629	chr21:15432744-15432745	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs112542280	chr21:15432764-15432765	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs374521882	chr21:15432765-15432766	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs553238799	chr21:15432768-15432769	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs71330961	chr21:15432774-15432775	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs71330962	chr21:15432785-15432786	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs71330963	chr21:15432791-15432792	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs200673755	chr21:15432809-15432810	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs71330964	chr21:15432818-15432819	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs71330965	chr21:15432832-15432833	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs71330966	chr21:15432858-15432859	ZNF genes & repeats Weak transcription Enhancers	CpG island	1 gene(s)	Overlapped CNVs	n/a
43	rs541994974	chr21:15432861-15432862	ZNF genes & repeats Weak transcription Enhancers	CpG island	1 gene(s)	Overlapped CNVs	n/a
44	rs11911702	chr21:15432862-15432863	ZNF genes & repeats Weak transcription Enhancers	CpG island	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs71321930	chr21:15432880-15432881	ZNF genes & repeats Weak transcription Enhancers	CpG island	1 gene(s)	Overlapped CNVs	n/a
46	rs530386858	chr21:15432890-15432891	ZNF genes & repeats Weak transcription Enhancers	CpG island	1 gene(s)	Overlapped CNVs	n/a
47	rs544213837	chr21:15432907-15432908	ZNF genes & repeats Weak transcription Enhancers	CpG island	1 gene(s)	Overlapped CNVs	n/a
48	rs71330967	chr21:15432908-15432909	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs113294903	chr21:15432913-15432914	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs71330968	chr21:15432924-15432925	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:60)

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
Sudden cardiac death	19188705	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
Breast cancer	20409316	CNVD
Autism	18414403	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

Chromatin state (count:95 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:15401800-15452000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
2	chr21:15402600-15442400	Weak transcription	Dnd41	blood
3	chr21:15423000-15442200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr21:15423400-15455600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
5	chr21:15423600-15443000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
6	chr21:15425800-15443400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr21:15427000-15432000	ZNF genes & repeats	Fetal Stomach	stomach
8	chr21:15427000-15433000	ZNF genes & repeats	Fetal Brain Female	brain
9	chr21:15427200-15436200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
10	chr21:15428200-15436000	Weak transcription	Right Atrium	heart
11	chr21:15428800-15432200	ZNF genes & repeats	Brain Germinal Matrix	brain
12	chr21:15428800-15449000	Weak transcription	Fetal Lung	lung
13	chr21:15429200-15433800	Weak transcription	Thymus	Thymus
14	chr21:15429200-15436000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
15	chr21:15429400-15436000	Weak transcription	Pancreas	Pancrea
16	chr21:15430400-15432600	Weak transcription	Skeletal Muscle Female	skeletal muscle
17	chr21:15430400-15433400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
18	chr21:15430400-15442400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
19	chr21:15431000-15436000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
20	chr21:15431200-15436000	Weak transcription	Stomach Smooth Muscle	stomach
21	chr21:15431200-15436200	Weak transcription	Aorta	Aorta
22	chr21:15431400-15432000	Genic enhancers	Esophagus	oesophagus
23	chr21:15431400-15434200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
24	chr21:15431400-15434600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
25	chr21:15431800-15432000	Strong transcription	iPS DF 19.11 Cell Line	embryonic stem cell
26	chr21:15431800-15432000	Strong transcription	Ovary	ovary
27	chr21:15431800-15432600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
28	chr21:15431800-15432600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
29	chr21:15431800-15432600	Weak transcription	Gastric	stomach
30	chr21:15432000-15435400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
31	chr21:15432000-15435400	Weak transcription	Ovary	ovary
32	chr21:15432000-15435800	Weak transcription	Esophagus	oesophagus
33	chr21:15432600-15432800	ZNF genes & repeats	Brain Germinal Matrix	brain
34	chr21:15432600-15433000	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
35	chr21:15432600-15433000	ZNF genes & repeats	H9 Derived Neuron Cultured Cells	ES cell derived
36	chr21:15432600-15433000	ZNF genes & repeats	Fetal Stomach	stomach
37	chr21:15432600-15433000	Enhancers	Gastric	stomach
38	chr21:15433000-15434000	Weak transcription	Fetal Brain Female	brain
39	chr21:15433000-15436400	Weak transcription	Gastric	stomach
40	chr21:15433000-15442200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
41	chr21:15433000-15442400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
42	chr21:15434000-15437600	ZNF genes & repeats	Fetal Brain Female	brain
43	chr21:15434600-15437000	ZNF genes & repeats	Brain Germinal Matrix	brain
44	chr21:15435400-15435600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
45	chr21:15435400-15436600	ZNF genes & repeats	Foreskin Keratinocyte Primary Cells skin03	Skin
46	chr21:15435600-15436800	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
47	chr21:15435600-15436800	ZNF genes & repeats	Fetal Stomach	stomach
48	chr21:15435800-15436800	Active TSS	iPS-18 Cell Line	embryonic stem cell
49	chr21:15435800-15437200	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
50	chr21:15435800-15438400	Active TSS	Esophagus	oesophagus

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