Variant report

Variant	esv19216
Chromosome Location	chr21:15283220-15352389
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:427)
CpG islands
(count:427)
Chromatin interactive
region (count:0)
LncRNA
region (count:22)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:427 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr21:15295624-15295648	K562	blood:	n/a	n/a
2	ARID3A	chr21:15346922-15347270	K562	blood:	n/a	n/a
3	ARID3A	chr21:15346022-15346251	K562	blood:	n/a	n/a
4	ATF1	chr21:15342677-15342811	K562	blood:	n/a	n/a
5	BACH1	chr21:15347039-15347218	K562	blood:	n/a	n/a
6	BATF	chr21:15321908-15322326	GM12878	blood:	n/a	chr21:15322062-15322070
7	BATF	chr21:15319344-15319735	GM12878	blood:	n/a	n/a
8	BATF	chr21:15295228-15295568	GM12878	blood:	n/a	chr21:15295405-15295416
9	BATF	chr21:15319369-15319639	GM12878	blood:	n/a	n/a
10	BATF	chr21:15340388-15340909	GM12878	blood:	n/a	n/a
11	BATF	chr21:15315223-15315545	GM12878	blood:	n/a	n/a
12	BATF	chr21:15340450-15340827	GM12878	blood:	n/a	n/a
13	BATF	chr21:15295169-15295585	GM12878	blood:	n/a	chr21:15295405-15295416
14	BATF	chr21:15321950-15322323	GM12878	blood:	n/a	chr21:15322062-15322070
15	BATF	chr21:15293789-15294119	GM12878	blood:	n/a	chr21:15293876-15293886
16	BATF	chr21:15341379-15341645	GM12878	blood:	n/a	chr21:15341542-15341553
17	BATF	chr21:15315150-15315618	GM12878	blood:	n/a	n/a
18	BATF	chr21:15302414-15302611	GM12878	blood:	n/a	chr21:15302548-15302559
19	BATF	chr21:15293789-15294118	GM12878	blood:	n/a	chr21:15293876-15293886
20	BATF	chr21:15315664-15315881	GM12878	blood:	n/a	n/a
21	BCL11A	chr21:15328745-15328928	GM12878	blood:	n/a	n/a
22	BCL11A	chr21:15340450-15340836	GM12878	blood:	n/a	chr21:15340521-15340530 chr21:15340574-15340583
23	BCL11A	chr21:15319397-15319586	GM12878	blood:	n/a	n/a
24	BCL11A	chr21:15293842-15294225	GM12878	blood:	n/a	n/a
25	BCL11A	chr21:15340406-15340552	GM12878	blood:	n/a	chr21:15340521-15340530
26	BCL11A	chr21:15322021-15322201	GM12878	blood:	n/a	n/a
27	BCL11A	chr21:15321900-15322332	GM12878	blood:	n/a	n/a
28	BCL11A	chr21:15319352-15319733	GM12878	blood:	n/a	n/a
29	BCL11A	chr21:15315283-15315608	GM12878	blood:	n/a	n/a
30	BCL11A	chr21:15315306-15315658	GM12878	blood:	n/a	chr21:15315610-15315619
31	BHLHE40	chr21:15352368-15352716	GM12878	blood:	n/a	n/a
32	BHLHE40	chr21:15295613-15295821	K562	blood:	n/a	n/a
33	BHLHE40	chr21:15347507-15347656	K562	blood:	n/a	n/a
34	CBX3	chr21:15352365-15352825	K562	blood:	n/a	n/a
35	CCNT2	chr21:15295624-15295806	K562	blood:	n/a	n/a
36	CEBPB	chr21:15347031-15347099	K562	blood:	n/a	n/a
37	CEBPB	chr21:15346232-15346412	K562	blood:	n/a	n/a
38	CEBPB	chr21:15294348-15294556	IMR90	lung:	n/a	n/a
39	CEBPD	chr21:15295340-15295897	K562	blood:	n/a	n/a
40	CEBPD	chr21:15346361-15346742	K562	blood:	n/a	n/a
41	CTCF	chr21:15302540-15302690	SK-N-SH_RA	brain:	n/a	n/a
42	CTCF	chr21:15352322-15352926	K562	blood:	n/a	n/a
43	CTCF	chr21:15302640-15302790	NHDF-neo	bronchial:	n/a	n/a
44	CTCF	chr21:15302510-15302750	MCF-7	breast:	n/a	n/a
45	CTCF	chr21:15302456-15302656	IMR90	lung:	n/a	n/a
46	CTCF	chr21:15352243-15352965	K562	blood:	n/a	n/a
47	CTCF	chr21:15292952-15293068	GM13976	blood:	n/a	n/a
48	CTCF	chr21:15302533-15302739	MCF-7	breast:	n/a	n/a
49	CTCF	chr21:15320100-15320250	HEK293	kidney:	n/a	n/a
50	CTCF	chr21:15352275-15352980	A549	lung:	n/a	n/a

(count:427 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr21:15309634-15309684	AG04449	skin:	fetal
2	chr21:15352085-15352135	HEK293	kidney:	embryo
3	chr21:15309846-15309896	NB4	blood:	n/a
4	chr21:15352213-15352263	HCT-116	colon:	n/a
5	chr21:15309846-15309896	SK-N-SH	brain:	n/a
6	chr21:15352213-15352263	MCF-7	breast:	n/a
7	chr21:15311594-15311644	A549	lung:	n/a
8	chr21:15309724-15309774	HCF	heart:	n/a
9	chr21:15311594-15311644	MCF-7	breast:	n/a
10	chr21:15309846-15309896	HCT-116	colon:	n/a
11	chr21:15309724-15309774	AG09309	skin:	n/a
12	chr21:15309634-15309684	RPTEC	kidney:	n/a
13	chr21:15352213-15352263	CMK	blood:	n/a
14	chr21:15352085-15352135	SK-N-SH	brain:	n/a
15	chr21:15309724-15309774	PrEC	prostate:	n/a
16	chr21:15309846-15309896	BE2_C	brain:	n/a
17	chr21:15311594-15311644	SK-N-SH_RA	brain:	n/a
18	chr21:15309724-15309774	PANC-1	pancreas:	n/a
19	chr21:15309724-15309774	A549	lung:	n/a
20	chr21:15309846-15309896	ProgFib	skin:	n/a
21	chr21:15309724-15309774	HRE	kidney:	n/a
22	chr21:15352085-15352135	HAEpiC	amniotic membrane:	n/a
23	chr21:15309724-15309774	LNCaP	prostate:	n/a
24	chr21:15352085-15352135	HMEC	breast:	n/a
25	chr21:15352213-15352263	AG10803	skin:	n/a
26	chr21:15309634-15309684	HRPEpiC	eye:	n/a
27	chr21:15352085-15352135	SKMC	muscle:	n/a
28	chr21:15352085-15352135	HCF	heart:	n/a
29	chr21:15352085-15352135	HCT-116	colon:	n/a
30	chr21:15311594-15311644	HRE	kidney:	n/a
31	chr21:15309846-15309896	MCF-7	breast:	n/a
32	chr21:15307662-15307712	PANC-1	pancreas:	n/a
33	chr21:15311594-15311644	Jurkat	blood:	n/a
34	chr21:15307662-15307712	SK-N-SH	brain:	n/a
35	chr21:15352085-15352135	HRCEpiC	kidney:	n/a
36	chr21:15309846-15309896	HEEpiC	esophagus:	n/a
37	chr21:15307662-15307712	HUVEC	blood vessel:	n/a
38	chr21:15352085-15352135	ProgFib	skin:	n/a
39	chr21:15309634-15309684	Hepatocyte	liver:	n/a
40	chr21:15307662-15307712	HCT-116	colon:	n/a
41	chr21:15309634-15309684	SKMC	muscle:	n/a
42	chr21:15311594-15311644	K562	blood:	n/a
43	chr21:15307662-15307712	NH-A	brain:	n/a
44	chr21:15307662-15307712	SK-N-SH_RA	brain:	n/a
45	chr21:15309634-15309684	HUVEC	blood vessel:	n/a
46	chr21:15309724-15309774	NHBE	bronchial:	n/a
47	chr21:15309846-15309896	HEK293	kidney:	embryo
48	chr21:15309724-15309774	AG10803	skin:	n/a
49	chr21:15307662-15307712	GM12892	blood:	n/a
50	chr21:15309634-15309684	HIPEpiC	eye:	n/a

No data

(count:22 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-LIPI-4	chr21:15323388-15323460	NONHSAT081132
2	lnc-LIPI-4	chr21:15344317-15344450	NONHSAT081133
3	lnc-LIPI-4	chr21:15323388-15323460	NONHSAT081131
4	lnc-LIPI-4	chr21:15323553-15323581	NONHSAT081133
5	lnc-LIPI-4	chr21:15323388-15323460	NONHSAT081133
6	lnc-LIPI-4	chr21:15335061-15335192	NONHSAT081133
7	lnc-LIPI-4	chr21:15311695-15311749	NONHSAT081132
8	lnc-LIPI-4	chr21:15317360-15317430	NONHSAT081133
9	lnc-LIPI-4	chr21:15316065-15316183	NONHSAT081133
10	lnc-LIPI-4	chr21:15313136-15313299	NONHSAT081132
11	lnc-LIPI-4	chr21:15313136-15313299	NONHSAT081131
12	lnc-LIPI-4	chr21:15335061-15335106	NONHSAT081132
13	lnc-LIPI-4	chr21:15317360-15317430	NONHSAT081131
14	lnc-LIPI-4	chr21:15339702-15339757	NONHSAT081133
15	lnc-LIPI-4	chr21:15311567-15311749	NONHSAT081131
16	lnc-LIPI-4	chr21:15323553-15323581	NONHSAT081131
17	lnc-LIPI-4	chr21:15323553-15323581	NONHSAT081132
18	lnc-LIPI-4	chr21:15310267-15310388	NONHSAT081131
19	lnc-POTED-11	chr21:15286426-15287046	NONHSAT081129
20	lnc-LIPI-4	chr21:15342294-15342431	NONHSAT081133
21	lnc-LIPI-4	chr21:15342294-15342324	NONHSAT081131
22	lnc-LIPI-4	chr21:15317360-15317464	NONHSAT081132

No data

Variant related genes	Relation type
RNU6-954P	TF binding region
SNX18P13	TF binding region
RHOT1P2	TF binding region
ANKRD20A11P	TF binding region
RNU6-954P	CpG island
SNX18P13	CpG island
RHOT1P2	CpG island
ANKRD20A11P	CpG island

Extended variants
information (count: 4491 )
Associated
traits (count: 66 )

Variant overlapped rSNPs/rCNVs (count:4491 , 50 per page) page: 1 2 3 4 5 6 7 ... 90

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs112561523	chr21:15283221-15283222	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs2822246	chr21:15283236-15283237	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs405690	chr21:15283243-15283244	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs548363872	chr21:15283248-15283249	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs190855399	chr21:15283254-15283255	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs532388852	chr21:15283291-15283292	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs4818676	chr21:15283295-15283296	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs35642930	chr21:15283323-15283324	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs115686809	chr21:15283325-15283326	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs34399188	chr21:15283378-15283379	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs4816871	chr21:15283381-15283382	Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs537727153	chr21:15283396-15283397	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs146822713	chr21:15283408-15283409	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs376455864	chr21:15283417-15283418	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs35407671	chr21:15283421-15283422	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs556308332	chr21:15283422-15283423	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs569640988	chr21:15283438-15283439	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs4816872	chr21:15283450-15283451	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs34068294	chr21:15283451-15283452	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs187819238	chr21:15283455-15283456	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs423681	chr21:15283458-15283459	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs373300599	chr21:15283489-15283490	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs4818680	chr21:15283490-15283491	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs555099460	chr21:15283545-15283546	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs112454215	chr21:15283580-15283581	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs373513769	chr21:15283581-15283582	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs370061582	chr21:15283675-15283676	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs574945477	chr21:15283682-15283683	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs190951702	chr21:15283726-15283727	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs563465555	chr21:15283760-15283761	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs576955702	chr21:15283816-15283817	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs545780675	chr21:15283830-15283831	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs559531890	chr21:15283843-15283844	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs527532017	chr21:15283860-15283861	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs547382271	chr21:15283897-15283898	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs202239229	chr21:15283923-15283924	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs529935272	chr21:15283928-15283929	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs550028618	chr21:15283937-15283938	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs569752351	chr21:15283952-15283953	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs370996247	chr21:15283972-15283973	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs374758658	chr21:15284009-15284010	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs200778250	chr21:15284081-15284082	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs538779955	chr21:15284111-15284112	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs552199513	chr21:15284124-15284125	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs565544532	chr21:15284150-15284151	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs201289722	chr21:15284158-15284159	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs201730418	chr21:15284203-15284204	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs13046909	chr21:15284227-15284228	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs200228966	chr21:15284231-15284232	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs568807993	chr21:15284256-15284257	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:66)

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
Breast cancer	21509527	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
Myelofibrosis	22110671	CNVD
Congenital abnormalities	21549014	CNVD
Developmental delay	21549014	CNVD
Mental retardation	21549014	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
Melanoma	17363583	CNVD
Breast cancer	22522925	CNVD
Multiple myeloma	17550852	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:131 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:15277000-15292200	Weak transcription	Dnd41	blood
2	chr21:15292200-15296200	Enhancers	Dnd41	blood
3	chr21:15292800-15293200	Enhancers	K562	blood
4	chr21:15293200-15293600	Weak transcription	K562	blood
5	chr21:15293600-15296200	Enhancers	K562	blood
6	chr21:15295200-15295800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr21:15295200-15296200	Enhancers	ES-I3 Cell Line	embryonic stem cell
8	chr21:15295200-15296200	Enhancers	HMEC	breast
9	chr21:15295400-15295800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
10	chr21:15296200-15298000	Weak transcription	K562	blood
11	chr21:15296200-15307200	Weak transcription	Dnd41	blood
12	chr21:15298000-15298200	Enhancers	K562	blood
13	chr21:15301600-15308400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
14	chr21:15306000-15307400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
15	chr21:15307200-15307400	ZNF genes & repeats	Dnd41	blood
16	chr21:15307200-15309800	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
17	chr21:15307200-15309800	ZNF genes & repeats	Esophagus	oesophagus
18	chr21:15307400-15308000	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
19	chr21:15307400-15309200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
20	chr21:15307600-15309200	ZNF genes & repeats	Thymus	Thymus
21	chr21:15307800-15308600	ZNF genes & repeats	Brain Anterior Caudate	brain
22	chr21:15307800-15309800	ZNF genes & repeats	IMR90 fetal lung fibroblasts Cell Line	lung
23	chr21:15308000-15309800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
24	chr21:15308200-15309000	ZNF genes & repeats	Spleen	Spleen
25	chr21:15308400-15309000	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast
26	chr21:15308400-15309800	ZNF genes & repeats	Dnd41	blood
27	chr21:15308600-15309200	ZNF genes & repeats	Colonic Mucosa	Colon
28	chr21:15308600-15311200	Weak transcription	Brain Anterior Caudate	brain
29	chr21:15309000-15312600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
30	chr21:15309000-15314000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
31	chr21:15309200-15310000	Weak transcription	Colonic Mucosa	Colon
32	chr21:15309200-15311000	Weak transcription	Thymus	Thymus
33	chr21:15309800-15310400	Strong transcription	Dnd41	blood
34	chr21:15309800-15311200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
35	chr21:15309800-15311400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
36	chr21:15310400-15347400	Weak transcription	Dnd41	blood
37	chr21:15311200-15311400	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
38	chr21:15341400-15341800	Active TSS	A549	lung
39	chr21:15341400-15342000	Enhancers	HMEC	breast
40	chr21:15341400-15342800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
41	chr21:15341400-15342800	Enhancers	Hela-S3	cervix
42	chr21:15341400-15342800	Enhancers	K562	blood
43	chr21:15342000-15342600	Weak transcription	HMEC	breast
44	chr21:15342600-15342800	Enhancers	HMEC	breast
45	chr21:15342800-15345800	Weak transcription	K562	blood
46	chr21:15345800-15346400	Flanking Active TSS	K562	blood
47	chr21:15346000-15346200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
48	chr21:15346400-15346800	Enhancers	K562	blood
49	chr21:15346800-15347000	Flanking Active TSS	K562	blood
50	chr21:15347000-15347200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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