Variant report

Variant	nsv528495
Chromosome Location	chr21:48015869-48052838
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:225)
CpG islands
(count:980)
Chromatin interactive
region (count:38)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:225 , 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	ATF2	chr21:48028361-48029224	GM12878	blood:	n/a	n/a
2	ATF3	chr21:48017955-48018252	K562	blood:	n/a	chr21:48018068-48018088
3	BATF	chr21:48028436-48029053	GM12878	blood:	n/a	n/a
4	BATF	chr21:48028473-48028947	GM12878	blood:	n/a	n/a
5	BCLAF1	chr21:48025984-48026402	GM12878	blood:	n/a	n/a
6	BCLAF1	chr21:48028466-48029094	GM12878	blood:	n/a	n/a
7	CBX3	chr21:48017920-48018249	K562	blood:	n/a	n/a
8	CBX3	chr21:48017809-48018333	K562	blood:	n/a	n/a
9	CEBPB	chr21:48047791-48047968	K562	blood:	n/a	n/a
10	CEBPB	chr21:48047658-48048067	K562	blood:	n/a	n/a
11	CEBPB	chr21:48020264-48020558	K562	blood:	n/a	n/a
12	CTCF	chr21:48018048-48018372	K562	blood:	n/a	chr21:48018186-48018199
13	CTCF	chr21:48018165-48018252	K562	blood:	n/a	chr21:48018186-48018199
14	CTCF	chr21:48046860-48047010	HepG2	liver:	n/a	n/a
15	CTCF	chr21:48018100-48018250	GM12867	blood:	n/a	chr21:48018186-48018199
16	CTCF	chr21:48018005-48018273	K562	blood:	n/a	chr21:48018186-48018199
17	CTCF	chr21:48046900-48047050	HepG2	liver:	n/a	n/a
18	CTCF	chr21:48028993-48029068	GM12878	blood:	n/a	n/a
19	CTCF	chr21:48028977-48029064	GM10266	blood:	n/a	n/a
20	CTCF	chr21:48028820-48028970	GM12873	blood:	n/a	n/a
21	CTCF	chr21:48018020-48018170	K562	blood:	n/a	n/a
22	CTCF	chr21:48018080-48018230	K562	blood:	n/a	chr21:48018186-48018199
23	CTCF	chr21:48028680-48028830	GM12864	blood:	n/a	n/a
24	CTCF	chr21:48018049-48018377	K562	blood:	n/a	chr21:48018186-48018199
25	CTCF	chr21:48018060-48018210	Hela-S3	cervix:	n/a	chr21:48018186-48018199
26	EBF1	chr21:48025973-48026546	GM12878	blood:	n/a	n/a
27	EBF1	chr21:48042233-48042490	GM12878	blood:	n/a	n/a
28	EBF1	chr21:48026020-48026423	GM12878	blood:	n/a	n/a
29	EGR1	chr21:48024963-48025225	K562	blood:	n/a	chr21:48025215-48025224 chr21:48025099-48025108 chr21:48025096-48025109
30	EGR1	chr21:48024950-48025231	K562	blood:	n/a	chr21:48025215-48025224 chr21:48025099-48025108 chr21:48025096-48025109
31	EGR1	chr21:48039897-48040129	K562	blood:	n/a	n/a
32	EGR1	chr21:48018008-48018258	K562	blood:	n/a	chr21:48018193-48018206
33	EGR1	chr21:48024900-48025237	H1-hESC	embryonic stem cell:	n/a	chr21:48025215-48025224 chr21:48025099-48025108 chr21:48025096-48025109
34	EGR1	chr21:48039894-48040150	K562	blood:	n/a	n/a
35	EGR1	chr21:48018016-48018248	K562	blood:	n/a	chr21:48018193-48018206
36	EGR1	chr21:48024866-48025287	ECC-1	luminal epithelium:	n/a	chr21:48025215-48025224 chr21:48025099-48025108 chr21:48025096-48025109
37	ELF1	chr21:48017729-48017997	K562	blood:	n/a	chr21:48017927-48017938
38	ELF1	chr21:48017731-48018266	K562	blood:	n/a	chr21:48017927-48017938
39	ELF1	chr21:48024860-48025163	GM12878	blood:	n/a	n/a
40	ELF1	chr21:48042131-48042533	HepG2	liver:	n/a	chr21:48042242-48042254 chr21:48042469-48042480
41	ELF1	chr21:48042126-48042552	HepG2	liver:	n/a	chr21:48042242-48042254 chr21:48042469-48042480
42	ELF1	chr21:48026001-48026710	GM12878	blood:	n/a	chr21:48026169-48026182
43	ELF1	chr21:48042112-48042422	GM12878	blood:	n/a	chr21:48042242-48042254
44	ELF1	chr21:48018047-48018261	K562	blood:	n/a	n/a
45	ELF1	chr21:48025991-48026352	K562	blood:	n/a	chr21:48026169-48026182
46	ELF1	chr21:48017829-48018255	GM12878	blood:	n/a	chr21:48017927-48017938
47	ELF1	chr21:48042102-48042464	GM12878	blood:	n/a	chr21:48042242-48042254
48	EP300	chr21:48041999-48042536	HepG2	liver:	n/a	chr21:48042360-48042369 chr21:48042510-48042524 chr21:48042272-48042282 chr21:48042471-48042480
49	EP300	chr21:48041378-48041856	HepG2	liver:	n/a	n/a
50	EP300	chr21:48041959-48042528	HepG2	liver:	n/a	chr21:48042360-48042369 chr21:48042510-48042524 chr21:48042272-48042282 chr21:48042471-48042480

(count:980 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr21:48018790-48018840	SAEC	small airway:	n/a
2	chr21:48052757-48052807	HUVEC	blood vessel:	n/a
3	chr21:48025691-48025741	MCF10A-Er-Src	breast:	n/a
4	chr21:48024639-48024689	ProgFib	skin:	n/a
5	chr21:48018790-48018840	SAEC	small airway:	n/a
6	chr21:48052757-48052807	HUVEC	blood vessel:	n/a
7	chr21:48025691-48025741	MCF10A-Er-Src	breast:	n/a
8	chr21:48024639-48024689	ProgFib	skin:	n/a
9	chr21:48018608-48018658	HMEC	breast:	n/a
10	chr21:48026298-48026348	HCT-116	colon:	n/a
11	chr21:48026298-48026348	ECC-1	luminal epithelium:	n/a
12	chr21:48026181-48026231	HMEC	breast:	n/a
13	chr21:48024639-48024689	Hela-S3	cervix:	n/a
14	chr21:48025691-48025741	HepG2	liver:	n/a
15	chr21:48021941-48021991	AoSMC	blood vessel:	n/a
16	chr21:48018632-48018682	H1-hESC	embryonic stem cell:	embryo
17	chr21:48022339-48022389	Jurkat	blood:	n/a
18	chr21:48022339-48022389	HEK293	kidney:	embryo
19	chr21:48019296-48019346	BE2_C	brain:	n/a
20	chr21:48025100-48025150	HMEC	breast:	n/a
21	chr21:48018790-48018840	PFSK-1	brain:	n/a
22	chr21:48025155-48025205	HL-60	blood:	n/a
23	chr21:48025155-48025205	BE2_C	brain:	n/a
24	chr21:48019296-48019346	GM12891	blood:	n/a
25	chr21:48025155-48025205	Caco-2	colon:	n/a
26	chr21:48026298-48026348	BJ	skin:	n/a
27	chr21:48025691-48025741	HRE	kidney:	n/a
28	chr21:48026043-48026093	MCF-7	breast:	n/a
29	chr21:48019296-48019346	AG10803	skin:	n/a
30	chr21:48025155-48025205	ovcar-3	ovarian:	n/a
31	chr21:48017232-48017282	SKMC	muscle:	n/a
32	chr21:48025691-48025741	H1-hESC	embryonic stem cell:	embryo
33	chr21:48025155-48025205	GM12878	blood:	n/a
34	chr21:48025155-48025205	RPTEC	kidney:	n/a
35	chr21:48024683-48024733	GM06990	blood:	n/a
36	chr21:48024639-48024689	ECC-1	luminal epithelium:	n/a
37	chr21:48019296-48019346	H1-hESC	embryonic stem cell:	embryo
38	chr21:48024683-48024733	GM12891	blood:	n/a
39	chr21:48024639-48024689	H1-hESC	embryonic stem cell:	embryo
40	chr21:48026181-48026231	NHBE	bronchial:	n/a
41	chr21:48052757-48052807	HNPCEpiC	eye:	n/a
42	chr21:48026181-48026231	AG09319	gingival:	n/a
43	chr21:48052757-48052807	NT2-D1	testis:	n/a
44	chr21:48025691-48025741	HIPEpiC	eye:	n/a
45	chr21:48052757-48052807	MCF10A-Er-Src	breast:	n/a
46	chr21:48025691-48025741	HCM	heart:	n/a
47	chr21:48019296-48019346	HPAEpiC	pulmonary alveolar:	n/a
48	chr21:48018608-48018658	PFSK-1	brain:	n/a
49	chr21:48018632-48018682	PrEC	prostate:	n/a
50	chr21:48026043-48026093	H1-hESC	embryonic stem cell:	embryo

(count:38 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr21:48023339..48026982-chr21:48053855..48056881,6	MCF-7	breast:
2	chr21:48044131..48047004-chr21:48048003..48050751,2	MCF-7	breast:
3	chr21:48017805..48022026-chr21:48053687..48056894,4	K562	blood:
4	chr21:47986444..47988898-chr21:48015731..48017367,2	K562	blood:
5	chr21:48025603..48028303-chr21:48029330..48031658,3	MCF-7	breast:
6	chr21:47980753..47982887-chr21:48026648..48028879,2	MCF-7	breast:
7	chr21:48028979..48030812-chr21:48051870..48054019,2	K562	blood:
8	chr21:48048775..48050687-chr21:48053494..48055105,2	MCF-7	breast:
9	chr21:48021540..48023901-chr21:48055495..48057109,2	MCF-7	breast:
10	chr21:47920604..47922605-chr21:48015742..48017826,2	K562	blood:
11	chr21:48043406..48045723-chr21:48050633..48054621,3	K562	blood:
12	chr21:48021498..48023722-chr21:48025363..48027869,3	K562	blood:
13	chr21:48043562..48050060-chr21:48053506..48056859,7	MCF-7	breast:
14	chr21:48044131..48047004-chr21:48048003..48050751,2	MCF-7	breast:
15	chr21:48043406..48045723-chr21:48050633..48054621,3	K562	blood:
16	chr21:48044480..48047952-chr21:48055875..48058667,3	MCF-7	breast:
17	chr21:48042730..48044237-chr21:48044461..48046707,2	K562	blood:
18	chr21:48048002..48052146-chr21:48052427..48057052,6	K562	blood:
19	chr21:48024575..48027546-chr21:48055306..48056858,2	K562	blood:
20	chr21:48045325..48047440-chr21:48054807..48056877,2	K562	blood:
21	chr21:48013557..48016686-chr21:48017781..48019868,3	MCF-7	breast:
22	chr21:48016127..48018173-chr21:48020936..48022713,2	K562	blood:
23	chr21:48016422..48019126-chr21:48030129..48032645,2	K562	blood:
24	chr21:48043420..48045155-chr21:48055192..48058063,2	K562	blood:
25	chr21:48024544..48027148-chr21:48052838..48054939,2	K562	blood:
26	chr21:48042730..48044237-chr21:48044461..48046707,2	K562	blood:
27	chr21:48013557..48016686-chr21:48017781..48019868,3	MCF-7	breast:
28	chr21:48017941..48023722-chr21:48025363..48028133,5	K562	blood:
29	chr21:48028979..48030812-chr21:48051870..48054019,2	K562	blood:
30	chr21:48016127..48018173-chr21:48020936..48022713,2	K562	blood:
31	chr21:48025522..48028149-chr21:48060514..48063166,2	MCF-7	breast:
32	chr21:48027694..48030453-chr21:48039157..48041006,2	MCF-7	breast:
33	chr21:48019242..48021637-chr21:48023777..48026826,3	MCF-7	breast:
34	chr21:48010670..48012334-chr21:48047542..48049804,2	K562	blood:
35	chr21:48031009..48033882-chr21:48053845..48056552,2	MCF-7	breast:
36	chr21:48025603..48028303-chr21:48029330..48031658,3	MCF-7	breast:
37	chr21:48027694..48030453-chr21:48039157..48041006,2	MCF-7	breast:
38	chr21:48016422..48019126-chr21:48030129..48032645,2	K562	blood:

No data

Variant related genes	Relation type
PRMT2	TF binding region
S100B	TF binding region
PRMT2	CpG island
S100B	CpG island
ENSG00000160305	chromatin interactions
ENSG00000160310	chromatin interactions
ENSG00000160307	chromatin interactions

Extended variants
information (count: 1436 )
Associated
traits (count: 36 )

Variant overlapped rSNPs/rCNVs (count:1436 , 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	rs2839343	chr21:48015869-48015870	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs148008615	chr21:48015876-48015877	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs537411560	chr21:48015886-48015887	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs558651437	chr21:48015913-48015914	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs555499060	chr21:48015938-48015939	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs147436409	chr21:48015972-48015973	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs184351011	chr21:48016058-48016059	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs386819457	chr21:48016067-48016068	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs59220795	chr21:48016068-48016069	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
10	rs112345771	chr21:48016069-48016070	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs376496789	chr21:48016070-48016071	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs183963065	chr21:48016091-48016092	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs536880313	chr21:48016110-48016111	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs189367046	chr21:48016169-48016170	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs575185578	chr21:48016293-48016294	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs59454503	chr21:48016326-48016327	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs542578321	chr21:48016350-48016351	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs79527268	chr21:48016408-48016409	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs575034694	chr21:48016415-48016416	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs76359771	chr21:48016422-48016423	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs540963796	chr21:48016423-48016424	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs180741147	chr21:48016472-48016473	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs9974426	chr21:48016477-48016478	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
24	rs186652607	chr21:48016497-48016498	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs373930839	chr21:48016500-48016501	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs572824780	chr21:48016506-48016507	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs139176151	chr21:48016516-48016517	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs35657740	chr21:48016559-48016560	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs544992911	chr21:48016578-48016579	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs16979449	chr21:48016605-48016606	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs13046595	chr21:48016641-48016642	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs567544276	chr21:48016646-48016647	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs73907532	chr21:48016670-48016671	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs190999058	chr21:48016690-48016691	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs2839344	chr21:48016691-48016692	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs538414685	chr21:48016695-48016696	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs181577451	chr21:48016710-48016711	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs544424018	chr21:48016735-48016736	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs2839345	chr21:48016737-48016738	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs13050390	chr21:48016739-48016740	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs13050395	chr21:48016742-48016743	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs2839346	chr21:48016748-48016749	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs561274351	chr21:48016772-48016773	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs529479275	chr21:48016829-48016830	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs572745277	chr21:48016833-48016834	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs546904035	chr21:48016847-48016848	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs28524577	chr21:48016855-48016856	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs2839347	chr21:48016948-48016949	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
49	rs373361301	chr21:48017011-48017012	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs77739211	chr21:48017017-48017018	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	mRNA abundance

Variant related diseases (count:36)

Disease	PMID	Source
Down syndrome	17576883	CNVD
Acute promyelocytic leukemia	19109227	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Prostate cancer	19156837	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	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
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Autism	18414403	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Breast cancer	17899364	CNVD
Prostate cancer	20473283	CNVD
Chordoma	18071362	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 adenocarcinoma	17086460	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

Chromatin state (count:769 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:48006000-48018600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
2	chr21:48013600-48018800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr21:48014000-48018600	Weak transcription	Primary T cells from cord blood	blood
4	chr21:48014400-48018000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
5	chr21:48014600-48018600	Weak transcription	Brain Anterior Caudate	brain
6	chr21:48014800-48017600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
7	chr21:48015200-48016200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
8	chr21:48015200-48017800	Enhancers	Breast Myoepithelial Primary Cells	Breast
9	chr21:48015200-48018600	Weak transcription	Brain Cingulate Gyrus	brain
10	chr21:48015600-48016000	Enhancers	Brain Hippocampus Middle	brain
11	chr21:48015800-48016600	Enhancers	Brain Substantia Nigra	brain
12	chr21:48015800-48018600	Weak transcription	Cortex derived primary cultured neurospheres	brain
13	chr21:48016000-48016800	Enhancers	Fetal Muscle Leg	muscle
14	chr21:48016000-48016800	Enhancers	HepG2	liver
15	chr21:48016000-48018600	Weak transcription	Brain Hippocampus Middle	brain
16	chr21:48016200-48016600	Enhancers	Fetal Muscle Trunk	muscle
17	chr21:48016200-48017400	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
18	chr21:48016400-48016600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
19	chr21:48016600-48018000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
20	chr21:48016600-48018600	Weak transcription	Brain Substantia Nigra	brain
21	chr21:48016800-48018600	Weak transcription	Fetal Muscle Leg	muscle
22	chr21:48016800-48018600	Weak transcription	HepG2	liver
23	chr21:48017000-48018400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
24	chr21:48017200-48017600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
25	chr21:48017200-48017600	Enhancers	Osteobl	bone
26	chr21:48017400-48017800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
27	chr21:48017400-48019400	Enhancers	Primary T cells fromperipheralblood	blood
28	chr21:48017600-48017800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
29	chr21:48017600-48017800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
30	chr21:48017600-48018600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
31	chr21:48017600-48018600	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
32	chr21:48017600-48018800	Weak transcription	Osteobl	bone
33	chr21:48017600-48020200	Enhancers	Primary T killer naive cells fromperipheralblood	blood
34	chr21:48017800-48018000	ZNF genes & repeats	iPS DF 6.9 Cell Line	embryonic stem cell
35	chr21:48017800-48018000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
36	chr21:48017800-48018000	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
37	chr21:48017800-48018000	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
38	chr21:48017800-48018000	Enhancers	Gastric	stomach
39	chr21:48017800-48018000	Enhancers	Spleen	Spleen
40	chr21:48017800-48018200	ZNF genes & repeats	Primary hematopoietic stem cells short term culture	blood
41	chr21:48017800-48018600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
42	chr21:48017800-48018800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
43	chr21:48017800-48019200	Strong transcription	Foreskin Melanocyte Primary Cells skin01	Skin
44	chr21:48017800-48019400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
45	chr21:48017800-48020800	Enhancers	Primary T helper cells PMA-I stimulated	--
46	chr21:48018000-48018200	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin01	Skin
47	chr21:48018000-48018200	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
48	chr21:48018000-48018400	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
49	chr21:48018000-48018600	Strong transcription	Brain Dorsolateral Prefrontal Cortex	brain
50	chr21:48018000-48019000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived

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