Variant report

Variant	esv1837818
Chromosome Location	chr21:44949285-44987079
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:250)
CpG islands
(count:427)
Chromatin interactive
region (count:21)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:250 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr21:44978207-44978307	K562	blood:	n/a	n/a
2	BATF	chr21:44985047-44985543	GM12878	blood:	n/a	n/a
3	BCL11A	chr21:44985340-44985534	GM12878	blood:	n/a	n/a
4	BCL11A	chr21:44985063-44985593	GM12878	blood:	n/a	n/a
5	CBX3	chr21:44964126-44964411	K562	blood:	n/a	n/a
6	CBX3	chr21:44964108-44964401	K562	blood:	n/a	n/a
7	CBX3	chr21:44985147-44985491	K562	blood:	n/a	n/a
8	CEBPB	chr21:44960403-44960428	HepG2	liver:	n/a	n/a
9	CEBPB	chr21:44985002-44985512	GM12878	blood:	n/a	n/a
10	CEBPB	chr21:44956319-44956330	HepG2	liver:	n/a	n/a
11	CTCF	chr21:44965257-44965309	LNCaP	prostate:	n/a	n/a
12	CTCF	chr21:44982520-44982670	SAEC	small airway:	n/a	n/a
13	CTCF	chr21:44970220-44970370	GM12864	blood:	n/a	n/a
14	CTCF	chr21:44982580-44982730	NHEK	skin:	n/a	n/a
15	CTCF	chr21:44982540-44982690	HMEC	breast:	n/a	n/a
16	CTCF	chr21:44985950-44985988	Lung_OC	lung:	n/a	n/a
17	CTCF	chr21:44962382-44962431	MCF-7	breast:	n/a	n/a
18	E2F4	chr21:44963788-44963988	MCF10A-Er-Src	breast:	n/a	n/a
19	EBF1	chr21:44985179-44985426	GM12878	blood:	n/a	n/a
20	EBF1	chr21:44985131-44985519	GM12878	blood:	n/a	n/a
21	EP300	chr21:44985067-44985466	GM12878	blood:	n/a	n/a
22	EP300	chr21:44985066-44985537	GM12878	blood:	n/a	n/a
23	EP300	chr21:44969004-44970296	SK-N-SH	brain:	n/a	n/a
24	FOS	chr21:44968071-44968411	MCF10A-Er-Src	breast:	n/a	n/a
25	FOS	chr21:44982397-44982716	MCF10A-Er-Src	breast:	n/a	n/a
26	FOS	chr21:44957871-44958033	MCF10A-Er-Src	breast:	n/a	n/a
27	FOS	chr21:44982353-44982646	MCF10A-Er-Src	breast:	n/a	n/a
28	FOS	chr21:44982373-44982775	MCF10A-Er-Src	breast:	n/a	n/a
29	FOS	chr21:44982374-44982736	MCF10A-Er-Src	breast:	n/a	n/a
30	FOS	chr21:44967959-44968499	MCF10A-Er-Src	breast:	n/a	n/a
31	FOS	chr21:44957889-44958089	MCF10A-Er-Src	breast:	n/a	n/a
32	FOS	chr21:44968072-44968265	MCF10A-Er-Src	breast:	n/a	n/a
33	FOSL2	chr21:44985072-44985508	HepG2	liver:	n/a	n/a
34	FOSL2	chr21:44985242-44985569	HepG2	liver:	n/a	n/a
35	FOXA1	chr21:44985218-44985552	HepG2	liver:	n/a	n/a
36	FOXA2	chr21:44985272-44985577	A549	lung:	n/a	n/a
37	FOXM1	chr21:44985043-44985417	GM12878	blood:	n/a	n/a
38	GABPA	chr21:44985002-44985276	Hela-S3	cervix:	n/a	n/a
39	GATA1	chr21:44951291-44952022	PBDE	blood:	n/a	chr21:44951706-44951717 chr21:44951695-44951712 chr21:44951825-44951835 chr21:44951825-44951834 chr21:44951827-44951834
40	GATA2	chr21:44984999-44985586	K562	blood:	n/a	n/a
41	GATA2	chr21:44985701-44986077	K562	blood:	n/a	n/a
42	GATA3	chr21:44954397-44954552	SH-SY5Y	brain:	n/a	n/a
43	HEY1	chr21:44985003-44985544	HepG2	liver:	n/a	n/a
44	HEY1	chr21:44984961-44985625	K562	blood:	n/a	n/a
45	HEY1	chr21:44984916-44986069	K562	blood:	n/a	n/a
46	HEY1	chr21:44985026-44985512	HepG2	liver:	n/a	n/a
47	IRF1	chr21:44961801-44961915	K562	blood:	n/a	n/a
48	IRF4	chr21:44984976-44985594	GM12878	blood:	n/a	n/a
49	IRF4	chr21:44984978-44985566	GM12878	blood:	n/a	n/a
50	JUN	chr21:44965178-44965360	K562	blood:	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	chr21:44982367-44982417	HCT-116	colon:	n/a
2	chr21:44985491-44985541	ECC-1	luminal epithelium:	n/a
3	chr21:44985357-44985407	HCT-116	colon:	n/a
4	chr21:44985491-44985541	SK-N-MC	brain:	n/a
5	chr21:44985092-44985142	NHDF-neo	bronchial:	n/a
6	chr21:44985005-44985055	HRPEpiC	eye:	n/a
7	chr21:44983258-44983308	HL-60	blood:	n/a
8	chr21:44985491-44985541	U87	brain:	n/a
9	chr21:44982367-44982417	ProgFib	skin:	n/a
10	chr21:44985491-44985541	HPAEpiC	pulmonary alveolar:	n/a
11	chr21:44985357-44985407	HMEC	breast:	n/a
12	chr21:44982367-44982417	CMK	blood:	n/a
13	chr21:44949625-44949675	NHBE	bronchial:	n/a
14	chr21:44985005-44985055	NB4	blood:	n/a
15	chr21:44985357-44985407	AG09319	gingival:	n/a
16	chr21:44949625-44949675	GM06990	blood:	n/a
17	chr21:44985491-44985541	H1-hESC	embryonic stem cell:	embryo
18	chr21:44985092-44985142	HEK293	kidney:	embryo
19	chr21:44985491-44985541	HIPEpiC	eye:	n/a
20	chr21:44985092-44985142	HEEpiC	esophagus:	n/a
21	chr21:44949625-44949675	HCT-116	colon:	n/a
22	chr21:44985357-44985407	SAEC	small airway:	n/a
23	chr21:44949625-44949675	HEEpiC	esophagus:	n/a
24	chr21:44983258-44983308	BE2_C	brain:	n/a
25	chr21:44985005-44985055	IMR90	lung:	fetal
26	chr21:44985491-44985541	CMK	blood:	n/a
27	chr21:44985092-44985142	AG04449	skin:	fetal
28	chr21:44985092-44985142	NB4	blood:	n/a
29	chr21:44983258-44983308	H1-hESC	embryonic stem cell:	embryo
30	chr21:44985005-44985055	HCT-116	colon:	n/a
31	chr21:44985357-44985407	T-47D	breast:	n/a
32	chr21:44985357-44985407	NHDF-neo	bronchial:	n/a
33	chr21:44985491-44985541	BJ	skin:	n/a
34	chr21:44985005-44985055	SK-N-SH_RA	brain:	n/a
35	chr21:44985092-44985142	BE2_C	brain:	n/a
36	chr21:44985491-44985541	HUVEC	blood vessel:	n/a
37	chr21:44985005-44985055	PFSK-1	brain:	n/a
38	chr21:44983258-44983308	IMR90	lung:	fetal
39	chr21:44985005-44985055	HCF	heart:	n/a
40	chr21:44985092-44985142	H1-hESC	embryonic stem cell:	embryo
41	chr21:44983258-44983308	SAEC	small airway:	n/a
42	chr21:44985357-44985407	MCF10A-Er-Src	breast:	n/a
43	chr21:44985092-44985142	NH-A	brain:	n/a
44	chr21:44949625-44949675	SKMC	muscle:	n/a
45	chr21:44982367-44982417	NH-A	brain:	n/a
46	chr21:44985491-44985541	MCF-7	breast:	n/a
47	chr21:44985005-44985055	HEEpiC	esophagus:	n/a
48	chr21:44985491-44985541	HEEpiC	esophagus:	n/a
49	chr21:44985092-44985142	HRCEpiC	kidney:	n/a
50	chr21:44949625-44949675	LNCaP	prostate:	n/a

(count:21 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr21:44934950..44937426-chr21:44968683..44970792,2	MCF-7	breast:
2	chr21:44943572..44946304-chr21:44954087..44956765,2	MCF-7	breast:
3	chr21:44947553..44949798-chr21:44957726..44959833,2	MCF-7	breast:
4	chr21:44942860..44944768-chr21:44951008..44952674,2	MCF-7	breast:
5	chr21:44938458..44941358-chr21:44949820..44951384,2	MCF-7	breast:
6	chr21:44947553..44949798-chr21:44957726..44959833,2	MCF-7	breast:
7	chr21:44763218..44765944-chr21:44956072..44958791,2	MCF-7	breast:
8	chr21:44947794..44949507-chr21:44953072..44955279,2	K562	blood:
9	chr21:44931615..44933117-chr21:44949429..44951810,2	K562	blood:
10	chr21:44957548..44959787-chr21:44963365..44965721,2	MCF-7	breast:
11	chr17:49633269..49633778-chr21:44982417..44983007,2	MCF-7	breast:
12	chr21:44871717..44874236-chr21:44949940..44952677,2	K562	blood:
13	chr21:44961687..44963545-chr21:45030403..45032227,2	MCF-7	breast:
14	chr21:44920968..44924573-chr21:44951870..44954060,3	MCF-7	breast:
15	chr10:32308854..32309354-chr21:44951717..44952253,2	NB4	blood:
16	chr21:44976320..44978488-chr21:45138337..45140856,2	K562	blood:
17	chr21:44958599..44960833-chr21:45017380..45019102,2	MCF-7	breast:
18	chr21:44969676..44971768-chr21:44981571..44983402,2	MCF-7	breast:
19	chr21:44957548..44959787-chr21:44963365..44965721,2	MCF-7	breast:
20	chr21:44947794..44949507-chr21:44953072..44955279,2	K562	blood:
21	chr21:44929525..44932273-chr21:44950323..44952927,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RRP1B-5	chr21:44971110-44971481	NONHSAT082437

No data

Variant related genes	Relation type
H2BFS	TF binding region
RPL31P1	TF binding region
H2BFS	CpG island
RPL31P1	CpG island
ENSG00000214326	chromatin interactions
ENSG00000160209	chromatin interactions

Extended variants
information (count: 1371 )
Associated
traits (count: 98 )

Variant overlapped rSNPs/rCNVs (count:1371 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs162398	chr21:44949285-44949286	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs531437554	chr21:44949327-44949328	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs117271204	chr21:44949389-44949390	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs577917311	chr21:44949417-44949418	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs116501678	chr21:44949456-44949457	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs528909938	chr21:44949490-44949491	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs537223888	chr21:44949542-44949543	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs185976550	chr21:44949549-44949550	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs374576827	chr21:44949592-44949593	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs376493602	chr21:44949598-44949599	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs200576511	chr21:44949599-44949600	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs533028897	chr21:44949611-44949612	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs374399301	chr21:44949626-44949627	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs545004279	chr21:44949627-44949628	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs142483325	chr21:44949684-44949685	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs151327305	chr21:44949685-44949686	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs569469116	chr21:44949694-44949695	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs368184709	chr21:44949696-44949697	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs140530326	chr21:44949704-44949705	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs371732136	chr21:44949716-44949717	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs145814386	chr21:44949728-44949729	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs138290442	chr21:44949729-44949730	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs141315363	chr21:44949730-44949731	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs201950743	chr21:44949783-44949784	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs144975683	chr21:44949821-44949822	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs367605171	chr21:44949840-44949841	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs371758893	chr21:44949846-44949847	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs535054387	chr21:44949903-44949904	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs375428409	chr21:44949945-44949946	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs113204549	chr21:44949946-44949947	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs148143002	chr21:44949947-44949948	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs191415028	chr21:44949962-44949963	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs181436652	chr21:44949963-44949964	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs571761556	chr21:44949969-44949970	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs543241201	chr21:44949973-44949974	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs561853903	chr21:44950018-44950019	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs162399	chr21:44950020-44950021	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
38	rs141065896	chr21:44950164-44950165	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs559039299	chr21:44950198-44950199	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs533063567	chr21:44950214-44950215	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs116777892	chr21:44950261-44950262	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs150270378	chr21:44950280-44950281	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs162400	chr21:44950305-44950306	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
44	rs548891953	chr21:44950351-44950352	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs115770731	chr21:44950368-44950369	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs534783215	chr21:44950373-44950374	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs528310795	chr21:44950380-44950381	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs536681320	chr21:44950386-44950387	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs77615195	chr21:44950397-44950398	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs186905842	chr21:44950435-44950436	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:98)

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 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
High-grade prostatic intraepithelial neoplasia	16573809	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
Autism	18414403	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Breast cancer	21858162	CNVD
Neuroblastoma	18923191	CNVD
Breast cancer	17899364	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Prostate cancer	20473283	CNVD
Chordoma	18071362	CNVD
Breast cancer	21364760	CNVD
Glioblastoma multiforme	18628472	CNVD
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-syndromic sensorineural hearing loss	17457615	CNVD
Ewing''s sarcoma	21437220	CNVD
Lung adenocarcinoma	17086460	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Ovarian neoplasms	16753589	CNVD
Non-small cell lung cancer	21829676	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Gastric adenocarcinoma	19115996	CNVD
Acute myeloid leukemia	21358987	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Prostate cancer	23341502	CNVD
Ovarian cancer	21720365	CNVD
Urothelial carcinoma	21177765	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Prostate cancer	18632612	CNVD
Neuroblastoma	20406844	CNVD
Acute myeloid leukemia	21251322	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Cholangiocarcinoma	16830362	CNVD
Down syndrome	17334655	CNVD
Neuroticism	17667963	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Autoimmune polyendocrine syndrome	18200029	CNVD
Prostate cancer	19363497	CNVD
Lung cancer	17086460	CNVD
Olfactory neuroblastoma	18408657	CNVD
Salivary gland adenoid cystic carcinoma	17545515	CNVD
Multiple myeloma	16616336	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Breast cancer	21509527	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Breast cancer	17142309	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Cancer	20164919	CNVD

Chromatin state (count:164 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:44941000-44949400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
2	chr21:44943000-44949400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr21:44943400-44956800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
4	chr21:44943600-44952400	Weak transcription	HMEC	breast
5	chr21:44943600-44952600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
6	chr21:44945400-44949600	Strong transcription	HSMMtube	muscle
7	chr21:44945600-44951400	Weak transcription	Placenta Amnion	Placenta Amnion
8	chr21:44946800-44951600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
9	chr21:44946800-44962800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr21:44947600-44949800	Strong transcription	NHEK	skin
11	chr21:44947800-44949600	Strong transcription	HSMM	muscle
12	chr21:44949000-44949600	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
13	chr21:44949400-44949600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
14	chr21:44949400-44949800	Strong transcription	Breast Myoepithelial Primary Cells	Breast
15	chr21:44949600-44952200	Weak transcription	HSMM	muscle
16	chr21:44949600-44953200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
17	chr21:44949600-44957600	Weak transcription	HSMMtube	muscle
18	chr21:44949800-44952000	Weak transcription	NHEK	skin
19	chr21:44949800-44956800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
20	chr21:44950600-44951200	Bivalent Enhancer	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr21:44950800-44951200	Enhancers	HUES48 Cell Line	embryonic stem cell
22	chr21:44950800-44951400	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
23	chr21:44951000-44952200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
24	chr21:44951200-44951400	Flanking Bivalent TSS/Enh	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
25	chr21:44951200-44952000	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
26	chr21:44951200-44959400	Weak transcription	Right Atrium	heart
27	chr21:44951400-44951600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
28	chr21:44951400-44951600	Bivalent Enhancer	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr21:44951400-44951600	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
30	chr21:44951400-44952600	Enhancers	Placenta Amnion	Placenta Amnion
31	chr21:44951400-44955000	Weak transcription	A549	lung
32	chr21:44951600-44952000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
33	chr21:44951600-44952200	Bivalent Enhancer	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
34	chr21:44951800-44952000	Enhancers	K562	blood
35	chr21:44952000-44952200	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
36	chr21:44952000-44952200	Enhancers	NHEK	skin
37	chr21:44952200-44952400	Enhancers	HSMM	muscle
38	chr21:44952400-44952600	Enhancers	HMEC	breast
39	chr21:44952400-44962600	Weak transcription	HSMM	muscle
40	chr21:44952600-44952800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
41	chr21:44953200-44953800	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
42	chr21:44953800-44956600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
43	chr21:44955400-44955800	Weak transcription	NHEK	skin
44	chr21:44956600-44958000	Enhancers	Fetal Thymus	thymus
45	chr21:44956600-44958400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
46	chr21:44956800-44957000	Enhancers	Breast Myoepithelial Primary Cells	Breast
47	chr21:44956800-44958400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
48	chr21:44956800-44958800	Enhancers	HMEC	breast
49	chr21:44957000-44957400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
50	chr21:44957000-44957800	Enhancers	NHEK	skin

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