Variant report

Variant	nsv1066052
Chromosome Location	chr21:47982925-48050534
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:372)
CpG islands
(count:1039)
Chromatin interactive
region (count:55)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:372 , 50 per page) page: 1 2 3 4 5 6 7 8

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	BHLHE40	chr21:47983229-47983425	K562	blood:	n/a	n/a
8	BHLHE40	chr21:47984475-47984548	K562	blood:	n/a	n/a
9	CBX3	chr21:48014212-48014536	K562	blood:	n/a	n/a
10	CBX3	chr21:48017920-48018249	K562	blood:	n/a	n/a
11	CBX3	chr21:48017809-48018333	K562	blood:	n/a	n/a
12	CEBPB	chr21:48047658-48048067	K562	blood:	n/a	n/a
13	CEBPB	chr21:47989027-47989372	HepG2	liver:	n/a	n/a
14	CEBPB	chr21:48047791-48047968	K562	blood:	n/a	n/a
15	CEBPB	chr21:48020264-48020558	K562	blood:	n/a	n/a
16	CEBPB	chr21:47989029-47989304	A549	lung:	n/a	n/a
17	CEBPB	chr21:47988938-47989373	IMR90	lung:	n/a	n/a
18	CTCF	chr21:48046860-48047010	HepG2	liver:	n/a	n/a
19	CTCF	chr21:47987940-47988090	HL-60	blood:	n/a	n/a
20	CTCF	chr21:48018005-48018273	K562	blood:	n/a	chr21:48018186-48018199
21	CTCF	chr21:48028977-48029064	GM10266	blood:	n/a	n/a
22	CTCF	chr21:48018049-48018377	K562	blood:	n/a	chr21:48018186-48018199
23	CTCF	chr21:48028680-48028830	GM12864	blood:	n/a	n/a
24	CTCF	chr21:47988007-47988145	HepG2	liver:	n/a	n/a
25	CTCF	chr21:48028820-48028970	GM12873	blood:	n/a	n/a
26	CTCF	chr21:47995160-47995310	MCF-7	breast:	n/a	n/a
27	CTCF	chr21:48028993-48029068	GM12878	blood:	n/a	n/a
28	CTCF	chr21:48018048-48018372	K562	blood:	n/a	chr21:48018186-48018199
29	CTCF	chr21:47988000-47988150	HCPEpiC	choroid plexus:	n/a	n/a
30	CTCF	chr21:48007283-48007335	LNCaP	prostate:	n/a	n/a
31	CTCF	chr21:47988074-47988126	MCF-7	breast:	n/a	n/a
32	CTCF	chr21:47988095-47988122	HepG2	liver:	n/a	n/a
33	CTCF	chr21:48015320-48015470	GM12866	blood:	n/a	n/a
34	CTCF	chr21:48018165-48018252	K562	blood:	n/a	chr21:48018186-48018199
35	CTCF	chr21:48018060-48018210	Hela-S3	cervix:	n/a	chr21:48018186-48018199
36	CTCF	chr21:48018020-48018170	K562	blood:	n/a	n/a
37	CTCF	chr21:47988020-47988170	WERI-Rb-1	eye:	n/a	n/a
38	CTCF	chr21:48018100-48018250	GM12867	blood:	n/a	chr21:48018186-48018199
39	CTCF	chr21:48008431-48008493	Spleen_OC	spleen:	n/a	n/a
40	CTCF	chr21:47988042-47988109	Hela-S3	cervix:	n/a	n/a
41	CTCF	chr21:48002020-48002170	HepG2	liver:	n/a	n/a
42	CTCF	chr21:48018080-48018230	K562	blood:	n/a	chr21:48018186-48018199
43	CTCF	chr21:47988076-47988108	MCF-7	breast:	n/a	n/a
44	CTCF	chr21:48046900-48047050	HepG2	liver:	n/a	n/a
45	EBF1	chr21:48025973-48026546	GM12878	blood:	n/a	n/a
46	EBF1	chr21:48026020-48026423	GM12878	blood:	n/a	n/a
47	EBF1	chr21:48042233-48042490	GM12878	blood:	n/a	n/a
48	EGR1	chr21:48018016-48018248	K562	blood:	n/a	chr21:48018193-48018206
49	EGR1	chr21:48024866-48025287	ECC-1	luminal epithelium:	n/a	chr21:48025215-48025224 chr21:48025099-48025108 chr21:48025096-48025109
50	EGR1	chr21:48024900-48025237	H1-hESC	embryonic stem cell:	n/a	chr21:48025215-48025224 chr21:48025099-48025108 chr21:48025096-48025109

(count:1039 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr21:48025100-48025150	ProgFib	skin:	n/a
2	chr21:48018790-48018840	SK-N-SH_RA	brain:	n/a
3	chr21:48025100-48025150	ProgFib	skin:	n/a
4	chr21:48018790-48018840	SK-N-SH_RA	brain:	n/a
5	chr21:48021941-48021991	Hepatocyte	liver:	n/a
6	chr21:48018608-48018658	SK-N-MC	brain:	n/a
7	chr21:48025691-48025741	GM12891	blood:	n/a
8	chr21:48026181-48026231	HEK293	kidney:	embryo
9	chr21:48026043-48026093	PANC-1	pancreas:	n/a
10	chr21:48025100-48025150	PrEC	prostate:	n/a
11	chr21:48025100-48025150	CMK	blood:	n/a
12	chr21:48017232-48017282	ovcar-3	ovarian:	n/a
13	chr21:48018790-48018840	SAEC	small airway:	n/a
14	chr21:48018608-48018658	PANC-1	pancreas:	n/a
15	chr21:48017232-48017282	LNCaP	prostate:	n/a
16	chr21:48017232-48017282	NT2-D1	testis:	n/a
17	chr21:47987607-47987657	SK-N-SH_RA	brain:	n/a
18	chr21:48019296-48019346	PFSK-1	brain:	n/a
19	chr21:48021941-48021991	Jurkat	blood:	n/a
20	chr21:48024639-48024689	BE2_C	brain:	n/a
21	chr21:48025691-48025741	HCPEpiC	choroid plexus:	n/a
22	chr21:48026043-48026093	NHBE	bronchial:	n/a
23	chr21:48018608-48018658	NHDF-neo	bronchial:	n/a
24	chr21:48026181-48026231	SKMC	muscle:	n/a
25	chr21:48021941-48021991	ECC-1	luminal epithelium:	n/a
26	chr21:48026181-48026231	BJ	skin:	n/a
27	chr21:48022339-48022389	SK-N-SH	brain:	n/a
28	chr21:48025100-48025150	NHBE	bronchial:	n/a
29	chr21:48022339-48022389	HEEpiC	esophagus:	n/a
30	chr21:48026298-48026348	NH-A	brain:	n/a
31	chr21:48024683-48024733	GM19239	blood:	n/a
32	chr21:48026043-48026093	HCPEpiC	choroid plexus:	n/a
33	chr21:48026043-48026093	HRE	kidney:	n/a
34	chr21:48025100-48025150	AG04450	lung:	fetal
35	chr21:48018632-48018682	MCF10A-Er-Src	breast:	n/a
36	chr21:48021941-48021991	GM06990	blood:	n/a
37	chr21:48018790-48018840	IMR90	lung:	fetal
38	chr21:48024683-48024733	LNCaP	prostate:	n/a
39	chr21:48024683-48024733	HCM	heart:	n/a
40	chr21:48021941-48021991	HRPEpiC	eye:	n/a
41	chr21:48026298-48026348	HAEpiC	amniotic membrane:	n/a
42	chr21:48019296-48019346	AoSMC	blood vessel:	n/a
43	chr21:48019296-48019346	Jurkat	blood:	n/a
44	chr21:47987607-47987657	K562	blood:	n/a
45	chr21:48017232-48017282	HMEC	breast:	n/a
46	chr21:48024639-48024689	ProgFib	skin:	n/a
47	chr21:48021941-48021991	HIPEpiC	eye:	n/a
48	chr21:48022339-48022389	NHBE	bronchial:	n/a
49	chr21:48022339-48022389	HNPCEpiC	eye:	n/a
50	chr21:48025100-48025150	PFSK-1	brain:	n/a

(count:55 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr21:47986444..47988898-chr21:48015731..48017367,2	K562	blood:
2	chr21:48024575..48027546-chr21:48055306..48056858,2	K562	blood:
3	chr21:47974804..47979372-chr21:47979836..47984256,6	MCF-7	breast:
4	chr21:48048002..48052146-chr21:48052427..48057052,6	K562	blood:
5	chr21:48013557..48016686-chr21:48017781..48019868,3	MCF-7	breast:
6	chr21:47971877..47975830-chr21:47983188..47986029,3	K562	blood:
7	chr21:48045325..48047440-chr21:48054807..48056877,2	K562	blood:
8	chr21:48044131..48047004-chr21:48048003..48050751,2	MCF-7	breast:
9	chr21:47990428..47992783-chr21:47994801..47997759,2	K562	blood:
10	chr21:48013557..48016686-chr21:48017781..48019868,3	MCF-7	breast:
11	chr21:48019242..48021637-chr21:48023777..48026826,3	MCF-7	breast:
12	chr21:48010670..48012334-chr21:48047542..48049804,2	K562	blood:
13	chr21:47990428..47992783-chr21:47994801..47997759,2	K562	blood:
14	chr21:48016422..48019126-chr21:48030129..48032645,2	K562	blood:
15	chr21:47995242..47996902-chr21:48001318..48004298,2	K562	blood:
16	chr21:48005218..48007630-chr21:48055834..48057649,2	K562	blood:
17	chr21:47980753..47982887-chr21:48026648..48028879,2	MCF-7	breast:
18	chr21:47977884..47980372-chr21:47985950..47987706,2	K562	blood:
19	chr21:47877021..47880570-chr21:47984512..47987705,4	K562	blood:
20	chr21:48025603..48028303-chr21:48029330..48031658,3	MCF-7	breast:
21	chr21:48043562..48050060-chr21:48053506..48056859,7	MCF-7	breast:
22	chr21:48044131..48047004-chr21:48048003..48050751,2	MCF-7	breast:
23	chr21:48027694..48030453-chr21:48039157..48041006,2	MCF-7	breast:
24	chr21:48002194..48004914-chr21:48055144..48057333,3	MCF-7	breast:
25	chr21:47980561..47982874-chr21:47984744..47986654,2	MCF-7	breast:
26	chr21:48021498..48023722-chr21:48025363..48027869,3	K562	blood:
27	chr21:47872410..47874001-chr21:47987885..47990582,2	K562	blood:
28	chr21:48025522..48028149-chr21:48060514..48063166,2	MCF-7	breast:
29	chr21:48017805..48022026-chr21:48053687..48056894,4	K562	blood:
30	chr21:48003128..48004642-chr21:48053741..48055698,2	MCF-7	breast:
31	chr21:48010670..48012334-chr21:48047542..48049804,2	K562	blood:
32	chr21:48028979..48030812-chr21:48051870..48054019,2	K562	blood:
33	chr21:48042730..48044237-chr21:48044461..48046707,2	K562	blood:
34	chr21:48025603..48028303-chr21:48029330..48031658,3	MCF-7	breast:
35	chr21:47986444..47988898-chr21:48015731..48017367,2	K562	blood:
36	chr21:47984970..47986522-chr21:48008602..48011495,2	K562	blood:
37	chr21:48021540..48023901-chr21:48055495..48057109,2	MCF-7	breast:
38	chr21:47984970..47986522-chr21:48008602..48011495,2	K562	blood:
39	chr21:47995242..47996902-chr21:48001318..48004298,2	K562	blood:
40	chr21:48044480..48047952-chr21:48055875..48058667,3	MCF-7	breast:
41	chr21:47973166..47976163-chr21:48002439..48005009,2	K562	blood:
42	chr21:48042730..48044237-chr21:48044461..48046707,2	K562	blood:
43	chr21:48027694..48030453-chr21:48039157..48041006,2	MCF-7	breast:
44	chr21:47920604..47922605-chr21:48015742..48017826,2	K562	blood:
45	chr21:48023339..48026982-chr21:48053855..48056881,6	MCF-7	breast:
46	chr21:48043406..48045723-chr21:48050633..48054621,3	K562	blood:
47	chr21:47982466..47985451-chr21:47987034..47988568,2	MCF-7	breast:
48	chr21:47986038..47989683-chr21:48053926..48057221,4	MCF-7	breast:
49	chr21:48043420..48045155-chr21:48055192..48058063,2	K562	blood:
50	chr21:48016422..48019126-chr21:48030129..48032645,2	K562	blood:

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	DIP2A	hsa-miR-125a-5p	chr21:47989806-47989829

Variant related genes	Relation type
DIP2A	TF binding region
PRMT2	TF binding region
S100B	TF binding region
DIP2A	CpG island
PRMT2	CpG island
S100B	CpG island
ENSG00000160310	chromatin interactions
ENSG00000160305	chromatin interactions
ENSG00000160307	chromatin interactions

Extended variants
information (count: 2721 )
Associated
traits (count: 36 )

Variant overlapped rSNPs/rCNVs (count:2721 , 50 per page) page: 1 2 3 4 5 6 7 ... 55

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs549990715	chr21:47982950-47982951	Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs112691003	chr21:47983017-47983018	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs146605910	chr21:47983073-47983074	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs743349	chr21:47983089-47983090	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs141455345	chr21:47983096-47983097	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs8127425	chr21:47983121-47983122	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs193172731	chr21:47983123-47983124	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs138925665	chr21:47983205-47983206	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs550445130	chr21:47983245-47983246	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs576484806	chr21:47983265-47983266	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs543639420	chr21:47983295-47983296	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs115728142	chr21:47983303-47983304	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs117311752	chr21:47983304-47983305	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs541334521	chr21:47983311-47983312	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs149038483	chr21:47983348-47983349	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs543367411	chr21:47983356-47983357	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs62225717	chr21:47983379-47983380	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs143002021	chr21:47983388-47983389	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs111647996	chr21:47983394-47983395	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs183324876	chr21:47983431-47983432	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs549955915	chr21:47983476-47983477	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs2070431	chr21:47983543-47983544	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
23	rs189074363	chr21:47983614-47983615	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs548083722	chr21:47983627-47983628	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs112065199	chr21:47983631-47983632	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs538893506	chr21:47983632-47983633	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs114660007	chr21:47983639-47983640	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs762253	chr21:47983657-47983658	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
29	rs538277707	chr21:47983666-47983667	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs762254	chr21:47983680-47983681	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
31	rs540737631	chr21:47983692-47983693	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs371829020	chr21:47983725-47983726	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs200045627	chr21:47983733-47983734	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs573901139	chr21:47983739-47983740	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs541299761	chr21:47983768-47983769	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs368827348	chr21:47983782-47983783	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs201790767	chr21:47983806-47983807	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs199921671	chr21:47983819-47983820	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs373337235	chr21:47983848-47983849	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs377397326	chr21:47983877-47983878	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs743350	chr21:47983975-47983976	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs79694455	chr21:47983979-47983980	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs193016862	chr21:47983993-47983994	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs561909948	chr21:47983996-47983997	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs529429196	chr21:47984003-47984004	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs147418001	chr21:47984030-47984031	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs62225718	chr21:47984105-47984106	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs138094396	chr21:47984142-47984143	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs73375721	chr21:47984171-47984172	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs533495364	chr21:47984177-47984178	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

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:1560 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:47943600-47990600	Strong transcription	Fetal Stomach	stomach
2	chr21:47947600-47989000	Strong transcription	Dnd41	blood
3	chr21:47947600-47991000	Strong transcription	Fetal Muscle Leg	muscle
4	chr21:47948400-47993600	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
5	chr21:47948600-47993200	Strong transcription	Fetal Intestine Large	intestine
6	chr21:47949000-47988200	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
7	chr21:47949000-47993600	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
8	chr21:47949800-47991800	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
9	chr21:47950000-47989200	Strong transcription	Skeletal Muscle Female	skeletal muscle
10	chr21:47950000-47991000	Strong transcription	Sigmoid Colon	Sigmoid Colon
11	chr21:47950200-47993200	Strong transcription	Stomach Smooth Muscle	stomach
12	chr21:47953000-47988200	Strong transcription	Gastric	stomach
13	chr21:47953000-47988600	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
14	chr21:47953200-47983400	Strong transcription	Brain Inferior Temporal Lobe	brain
15	chr21:47953200-47988400	Strong transcription	Fetal Intestine Small	intestine
16	chr21:47953200-47993000	Strong transcription	Osteobl	bone
17	chr21:47953400-47988000	Strong transcription	Cortex derived primary cultured neurospheres	brain
18	chr21:47956200-48001800	Weak transcription	Stomach Mucosa	stomach
19	chr21:47959200-47983400	Weak transcription	Pancreatic Islets	Pancreatic Islet
20	chr21:47961600-47992800	Strong transcription	Brain Hippocampus Middle	brain
21	chr21:47964600-47988400	Strong transcription	Brain Germinal Matrix	brain
22	chr21:47965200-47991200	Strong transcription	HUES6 Cell Line	embryonic stem cell
23	chr21:47965800-47988600	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
24	chr21:47965800-47993400	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
25	chr21:47966200-47993400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
26	chr21:47966400-47987800	Strong transcription	Muscle Satellite Cultured Cells	--
27	chr21:47966600-47988200	Strong transcription	Esophagus	oesophagus
28	chr21:47966800-47985400	Strong transcription	HMEC	breast
29	chr21:47966800-47985800	Weak transcription	K562	blood
30	chr21:47967400-47994800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
31	chr21:47968600-47990800	Strong transcription	Fetal Brain Female	brain
32	chr21:47969400-47987600	Strong transcription	Aorta	Aorta
33	chr21:47969600-47988200	Strong transcription	Brain Dorsolateral Prefrontal Cortex	brain
34	chr21:47969600-47988400	Strong transcription	Colonic Mucosa	Colon
35	chr21:47969800-47989200	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
36	chr21:47970200-47992400	Strong transcription	Duodenum Smooth Muscle	Duodenum
37	chr21:47970400-47988200	Strong transcription	Placenta Amnion	Placenta Amnion
38	chr21:47970400-47993200	Strong transcription	Brain Cingulate Gyrus	brain
39	chr21:47971000-47989200	Strong transcription	Placenta	Placenta
40	chr21:47971600-47991600	Strong transcription	Brain Substantia Nigra	brain
41	chr21:47972000-47988800	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
42	chr21:47973200-47993000	Strong transcription	Duodenum Mucosa	Duodenum
43	chr21:47973400-47993200	Strong transcription	Rectal Smooth Muscle	rectum
44	chr21:47973600-47989600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
45	chr21:47973600-47990600	Strong transcription	Breast Myoepithelial Primary Cells	Breast
46	chr21:47973600-47991600	Strong transcription	Rectal Mucosa Donor 31	rectum
47	chr21:47973600-47992600	Strong transcription	Monocytes-CD14+_RO01746	blood
48	chr21:47973800-47983200	Strong transcription	Primary neutrophils fromperipheralblood	blood
49	chr21:47973800-47984200	Strong transcription	Brain Angular Gyrus	brain
50	chr21:47973800-47990600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--

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