Variant report

Variant	esv2762111
Chromosome Location	chr21:37967924-38023546
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:760)
CpG islands
(count:0)
Chromatin interactive
region (count:49)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:760 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr21:38020070-38020381	HepG2	liver:	n/a	n/a
2	ARID3A	chr21:37985492-37985692	HepG2	liver:	n/a	n/a
3	ARID3A	chr21:38003064-38003279	HepG2	liver:	n/a	n/a
4	ATF1	chr21:38020059-38020133	K562	blood:	n/a	n/a
5	ATF2	chr21:38003001-38003432	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr21:38003245-38003342	H1-hESC	embryonic stem cell:	n/a	n/a
7	BHLHE40	chr21:38001516-38001600	K562	blood:	n/a	n/a
8	BHLHE40	chr21:38003212-38003277	K562	blood:	n/a	n/a
9	BHLHE40	chr21:38020102-38020331	HepG2	liver:	n/a	n/a
10	BHLHE40	chr21:37985495-37985589	HepG2	liver:	n/a	n/a
11	BHLHE40	chr21:38003195-38003315	GM12878	blood:	n/a	n/a
12	BRCA1	chr21:37969586-37969647	GM12878	blood:	n/a	n/a
13	BRCA1	chr21:38003205-38003264	H1-hESC	embryonic stem cell:	n/a	n/a
14	BRCA1	chr21:38003327-38003369	GM12878	blood:	n/a	n/a
15	CCNT2	chr21:38012806-38013006	K562	blood:	n/a	n/a
16	CEBPB	chr21:37997183-37997320	Hela-S3	cervix:	n/a	n/a
17	CEBPB	chr21:37975883-37975910	HepG2	liver:	n/a	chr21:37975891-37975902
18	CEBPB	chr21:38005669-38005795	HepG2	liver:	n/a	chr21:38005726-38005737
19	CEBPB	chr21:37973697-37974011	Hela-S3	cervix:	n/a	n/a
20	CEBPB	chr21:38020055-38020238	HepG2	liver:	n/a	n/a
21	CEBPB	chr21:37997116-37997372	HepG2	liver:	n/a	n/a
22	CEBPB	chr21:37985916-37986238	Hela-S3	cervix:	n/a	chr21:37986060-37986071
23	CEBPB	chr21:38012815-38013004	IMR90	lung:	n/a	n/a
24	CEBPB	chr21:37985913-37986249	A549	lung:	n/a	chr21:37986060-37986071
25	CEBPB	chr21:37985972-37986155	K562	blood:	n/a	chr21:37986060-37986071
26	CEBPB	chr21:37985845-37986205	MCF-7	breast:	n/a	chr21:37986060-37986071
27	CEBPB	chr21:38005632-38005832	IMR90	lung:	n/a	chr21:38005726-38005737
28	CEBPB	chr21:37977499-37977713	A549	lung:	n/a	chr21:37977575-37977586
29	CEBPB	chr21:37985918-37986213	IMR90	lung:	n/a	chr21:37986060-37986071
30	CEBPB	chr21:38013267-38013504	H1-hESC	embryonic stem cell:	n/a	n/a
31	CEBPB	chr21:37997070-37997433	A549	lung:	n/a	n/a
32	CEBPB	chr21:37997120-37997442	IMR90	lung:	n/a	n/a
33	CEBPB	chr21:38003172-38003421	H1-hESC	embryonic stem cell:	n/a	n/a
34	CEBPB	chr21:38003127-38003430	Hela-S3	cervix:	n/a	n/a
35	CEBPB	chr21:37986044-37986071	H1-hESC	embryonic stem cell:	n/a	chr21:37986060-37986071
36	CEBPB	chr21:37979932-37979958	HepG2	liver:	n/a	n/a
37	CEBPB	chr21:37977548-37977719	K562	blood:	n/a	chr21:37977575-37977586
38	CEBPB	chr21:38001475-38001558	K562	blood:	n/a	n/a
39	CEBPB	chr21:37985926-37986191	HepG2	liver:	n/a	chr21:37986060-37986071
40	CEBPB	chr21:38012733-38013103	Hela-S3	cervix:	n/a	n/a
41	CEBPB	chr21:37977415-37977724	HepG2	liver:	n/a	chr21:37977575-37977586
42	CHD1	chr21:38003120-38003290	H1-hESC	embryonic stem cell:	n/a	n/a
43	CHD2	chr21:38013310-38013381	H1-hESC	embryonic stem cell:	n/a	n/a
44	CHD2	chr21:38003151-38003274	H1-hESC	embryonic stem cell:	n/a	n/a
45	CTCF	chr21:38003140-38003290	GM12865	blood:	n/a	chr21:38003207-38003220 chr21:38003207-38003220 chr21:38003204-38003222 chr21:38003207-38003216 chr21:38003209-38003219 chr21:38003206-38003227 chr21:38003205-38003221
46	CTCF	chr21:38013220-38013370	HepG2	liver:	n/a	n/a
47	CTCF	chr21:38013320-38013470	GM12873	blood:	n/a	n/a
48	CTCF	chr21:37987800-37987950	HRE	kidney:	n/a	n/a
49	CTCF	chr21:37987682-37987881	GM12878	blood:	n/a	n/a
50	CTCF	chr21:37987700-37987850	AG04450	lung:	n/a	n/a

No data

(count:49 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:20299715..20301403-chr21:38005000..38006593,2	MCF-7	breast:
2	chr21:37794914..37795627-chr21:38007603..38008381,2	MCF-7	breast:
3	chr21:38002757..38003438-chr21:38311864..38312417,2	K562	blood:
4	chr21:37972910..37975712-chr21:37978328..37980849,2	MCF-7	breast:
5	chr21:38009294..38012972-chr21:38013930..38015457,3	K562	blood:
6	chr21:38012217..38014977-chr21:38016045..38018740,3	MCF-7	breast:
7	chr21:38013864..38015523-chr21:38031564..38034377,2	K562	blood:
8	chr21:38003011..38003670-chr21:38119687..38120282,3	MCF-7	breast:
9	chr21:38009294..38011893-chr21:38013930..38015440,2	K562	blood:
10	chr21:37970149..37972535-chr21:37972835..37974907,2	K562	blood:
11	chr21:37794982..37796991-chr21:37998830..38001272,2	K562	blood:
12	chr21:38002649..38006364-chr21:38007976..38010340,3	MCF-7	breast:
13	chr21:38002688..38003668-chr21:38226578..38227441,3	MCF-7	breast:
14	chr21:38012217..38014977-chr21:38016045..38018740,3	MCF-7	breast:
15	chr21:37972910..37975712-chr21:37978328..37980849,2	MCF-7	breast:
16	chr21:37987143..37987862-chr21:38002899..38003681,3	MCF-7	breast:
17	chr21:37970149..37972535-chr21:37972835..37974907,2	K562	blood:
18	chr21:38004251..38005826-chr21:38011095..38012905,2	MCF-7	breast:
19	chr21:37993760..37996592-chr21:38001803..38004283,2	MCF-7	breast:
20	chr21:37900509..37902393-chr21:38014528..38016261,2	MCF-7	breast:
21	chr21:38002701..38004136-chr21:38299631..38300607,8	K562	blood:
22	chr21:38001387..38003379-chr21:38011716..38014513,2	K562	blood:
23	chr21:38019419..38021646-chr21:38023297..38025801,2	MCF-7	breast:
24	chr21:37966496..37969164-chr21:37974994..37977509,2	K562	blood:
25	chr21:37958771..37961149-chr21:37984167..37986664,2	MCF-7	breast:
26	chr21:37873311..37874137-chr21:37985296..37985906,2	MCF-7	breast:
27	chr21:38002158..38005829-chr21:38006876..38010739,3	K562	blood:
28	chr21:37975190..37976872-chr21:37977276..37978822,2	K562	blood:
29	chr21:38014813..38017005-chr21:38019870..38021539,2	K562	blood:
30	chr21:37876312..37877270-chr21:37987783..37988597,2	MCF-7	breast:
31	chr21:37973420..37975043-chr21:37996316..37998941,2	K562	blood:
32	chr21:38019419..38021646-chr21:38023297..38025801,2	MCF-7	breast:
33	chr21:37960058..37963190-chr21:37967136..37970728,3	K562	blood:
34	chr21:37961845..37963348-chr21:37965336..37968270,2	K562	blood:
35	chr21:38014017..38016313-chr21:38020039..38021948,2	K562	blood:
36	chr21:37975190..37976872-chr21:37977276..37978822,2	K562	blood:
37	chr21:37973420..37975043-chr21:37996316..37998941,2	K562	blood:
38	chr21:37993760..37996592-chr21:38001803..38004283,2	MCF-7	breast:
39	chr21:38014017..38016313-chr21:38020039..38021948,2	K562	blood:
40	chr21:37797860..37800286-chr21:37973474..37976401,2	MCF-7	breast:
41	chr21:38004251..38005826-chr21:38011095..38012905,2	MCF-7	breast:
42	chr21:38014023..38015744-chr21:38032650..38034377,2	K562	blood:
43	chr21:38010914..38013220-chr21:38015944..38018928,2	MCF-7	breast:
44	chr21:37987143..37987862-chr21:38002899..38003681,3	MCF-7	breast:
45	chr21:38014813..38017005-chr21:38019870..38021539,2	K562	blood:
46	chr21:38010914..38013220-chr21:38015944..38018928,2	MCF-7	breast:
47	chr21:37966496..37969164-chr21:37974994..37977509,2	K562	blood:
48	chr21:38001387..38003379-chr21:38011716..38014513,2	K562	blood:
49	chr21:37987249..37987877-chr21:38299679..38300587,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CLDN14-1	chr21:38004979-38005868	XLOC_014068
2	lnc-CLDN14-1	chr21:38009089-38009331	XLOC_014068

No data

Variant related genes	Relation type
ENSG00000231324	TF binding region
ENSG00000231324	chromatin interactions

Extended variants
information (count: 2238 )
Associated
traits (count: 68 )

Variant overlapped rSNPs/rCNVs (count:2238 , 50 per page) page: 1 2 3 4 5 6 7 ... 45

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs117269230	chr21:37968009-37968010	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs111707169	chr21:37968049-37968050	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs2835398	chr21:37968106-37968107	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
4	rs140980943	chr21:37968125-37968126	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs566138245	chr21:37968205-37968206	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs535138023	chr21:37968263-37968264	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs555171364	chr21:37968305-37968306	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs543068457	chr21:37968386-37968387	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs575121379	chr21:37968451-37968452	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs537335550	chr21:37968474-37968475	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs561147050	chr21:37968488-37968489	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs557682951	chr21:37968500-37968501	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs577471282	chr21:37968501-37968502	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs544951048	chr21:37968590-37968591	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs370004605	chr21:37968613-37968614	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs573156438	chr21:37968621-37968622	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs571782328	chr21:37968652-37968653	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs540756598	chr21:37968693-37968694	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs34065849	chr21:37968709-37968710	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs560732383	chr21:37968749-37968750	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs529938485	chr21:37968757-37968758	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs77061104	chr21:37968802-37968803	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs553782395	chr21:37968826-37968827	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs563549142	chr21:37968832-37968833	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs532314689	chr21:37968855-37968856	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs2835399	chr21:37968894-37968895	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
27	rs566099741	chr21:37968918-37968919	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs565332040	chr21:37968920-37968921	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs114573378	chr21:37968921-37968922	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs568558993	chr21:37968965-37968966	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs189531632	chr21:37968977-37968978	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs557282205	chr21:37969057-37969058	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs79895613	chr21:37969065-37969066	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs193201067	chr21:37969096-37969097	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs144916895	chr21:37969122-37969123	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs539768767	chr21:37969148-37969149	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs558111379	chr21:37969151-37969152	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs571745359	chr21:37969178-37969179	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs560901117	chr21:37969183-37969184	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs540714924	chr21:37969206-37969207	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs554288514	chr21:37969216-37969217	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs34689132	chr21:37969219-37969220	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs532637435	chr21:37969233-37969234	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs550747179	chr21:37969238-37969239	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs201202218	chr21:37969252-37969253	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs55833466	chr21:37969284-37969285	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs34358980	chr21:37969304-37969305	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs55757209	chr21:37969310-37969311	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs543563239	chr21:37969313-37969314	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs563352903	chr21:37969325-37969326	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:68)

Disease	PMID	Source
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
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
Prostate cancer	19156837	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
small cell lung cancer	20016488	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
lymphocytic leukemia	21291569	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
Chronic lymphocytic leukemia	20421269	CNVD
Wilms tumour	21544195	CNVD
Ewing''s sarcoma	17952124	CNVD
Ovarian cancer	22174824	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Breast cancer	21364760	CNVD
Acute myeloid leukemia	16864856	CNVD
Mental retardation	21031080	CNVD
Polymicrogyria	21031080	CNVD
periventricular nodular heterotopia	21031080	CNVD
Myelodysplastic syndrome	21606161	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Acute myeloid leukemia	17237825	CNVD
Autism	18414403	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Breast cancer	21858162	CNVD
Neuroblastoma	18923191	CNVD
Breast cancer	17899364	CNVD
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Down syndrome	20877625	CNVD
Acute myeloid leukemia	21251322	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
T-cell lymphomas	22341440	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:241 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:37965600-37973000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr21:37970600-37974800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
3	chr21:37971800-37972000	Enhancers	Primary T helper naive cells fromperipheralblood	blood
4	chr21:37972200-37973400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
5	chr21:37973000-37973600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr21:37973400-37973600	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
7	chr21:37973400-37973800	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin03	Skin
8	chr21:37973400-37974200	Enhancers	Primary T helper naive cells from peripheral blood	blood
9	chr21:37973400-37975200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
10	chr21:37973600-37976400	Enhancers	Primary T cells fromperipheralblood	blood
11	chr21:37973600-37978800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
12	chr21:37974200-37974600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
13	chr21:37974200-37975200	Enhancers	Primary T cells from cord blood	blood
14	chr21:37974200-37975200	Enhancers	Primary T helper cells fromperipheralblood	blood
15	chr21:37974200-37976000	Enhancers	Primary T helper cells PMA-I stimulated	--
16	chr21:37974600-37977200	Enhancers	Primary T helper naive cells from peripheral blood	blood
17	chr21:37974800-37976600	Enhancers	Fetal Thymus	thymus
18	chr21:37974800-37976800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
19	chr21:37975000-37975800	Enhancers	Primary T killer memory cells from peripheral blood	blood
20	chr21:37975000-37976400	Enhancers	Thymus	Thymus
21	chr21:37975200-37975400	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
22	chr21:37975200-37975400	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
23	chr21:37975200-37975600	Flanking Active TSS	Primary T cells from cord blood	blood
24	chr21:37975400-37975600	Active TSS	Primary T helper cells fromperipheralblood	blood
25	chr21:37975400-37975800	Active TSS	Primary T helper naive cells fromperipheralblood	blood
26	chr21:37975600-37976400	Weak transcription	Primary T helper cells fromperipheralblood	blood
27	chr21:37975600-37976800	Enhancers	Primary T cells from cord blood	blood
28	chr21:37975600-37981800	Weak transcription	Right Atrium	heart
29	chr21:37975800-37976000	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
30	chr21:37976000-37976400	Weak transcription	Primary T helper cells PMA-I stimulated	--
31	chr21:37976000-37977000	Enhancers	Primary T helper naive cells fromperipheralblood	blood
32	chr21:37976400-37976800	Enhancers	Primary T helper cells PMA-I stimulated	--
33	chr21:37976400-37977200	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
34	chr21:37976600-37976800	Enhancers	Primary T helper cells fromperipheralblood	blood
35	chr21:37977400-37979600	Enhancers	Brain Cingulate Gyrus	brain
36	chr21:37977400-37979600	Enhancers	Brain Hippocampus Middle	brain
37	chr21:37977600-37977800	Enhancers	Fetal Kidney	kidney
38	chr21:37977600-37978200	Enhancers	Fetal Lung	lung
39	chr21:37977600-37978200	Enhancers	Spleen	Spleen
40	chr21:37977600-37979200	Enhancers	Brain Anterior Caudate	brain
41	chr21:37977600-37979400	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
42	chr21:37977600-37979400	Enhancers	Brain Substantia Nigra	brain
43	chr21:37977600-37979600	Enhancers	Brain Inferior Temporal Lobe	brain
44	chr21:37977800-37978800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
45	chr21:37977800-37979200	Enhancers	Brain Angular Gyrus	brain
46	chr21:37977800-37979600	Bivalent Enhancer	Fetal Muscle Trunk	muscle
47	chr21:37978000-37978200	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
48	chr21:37978000-37978600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
49	chr21:37978000-37979400	Enhancers	Cortex derived primary cultured neurospheres	brain
50	chr21:37978200-37978400	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin

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