Variant report

Variant	nsv880174
Chromosome Location	chr4:143639498-143848024
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1692)
CpG islands
(count:1221)
Chromatin interactive
region (count:55)
LncRNA
region (count:14)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1692 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr4:143737165-143737190	H1-hESC	embryonic stem cell:	n/a	n/a
2	BACH1	chr4:143768340-143768644	H1-hESC	embryonic stem cell:	n/a	n/a
3	BRCA1	chr4:143738598-143739035	Hela-S3	cervix:	n/a	n/a
4	CBX3	chr4:143640947-143641624	HCT-116	colon:	n/a	n/a
5	CBX3	chr4:143738385-143740006	HCT-116	colon:	n/a	n/a
6	CBX3	chr4:143723168-143723634	HCT-116	colon:	n/a	n/a
7	CBX3	chr4:143664207-143665012	HCT-116	colon:	n/a	n/a
8	CBX3	chr4:143738280-143739104	HCT-116	colon:	n/a	n/a
9	CEBPB	chr4:143738448-143739737	HCT-116	colon:	n/a	chr4:143738923-143738934 chr4:143738922-143738933 chr4:143738924-143738933
10	CEBPB	chr4:143738761-143739058	HepG2	liver:	n/a	chr4:143738923-143738934 chr4:143738922-143738933 chr4:143738924-143738933
11	CEBPB	chr4:143730724-143730997	IMR90	lung:	n/a	chr4:143730946-143730954 chr4:143730859-143730872
12	CEBPB	chr4:143698657-143698909	HepG2	liver:	n/a	n/a
13	CEBPB	chr4:143652895-143653164	IMR90	lung:	n/a	n/a
14	CEBPB	chr4:143698596-143698950	Hela-S3	cervix:	n/a	n/a
15	CEBPB	chr4:143647576-143647849	IMR90	lung:	n/a	chr4:143647716-143647729
16	CEBPB	chr4:143664062-143664720	HCT-116	colon:	n/a	chr4:143664319-143664330
17	CEBPB	chr4:143738788-143738977	H1-hESC	embryonic stem cell:	n/a	chr4:143738923-143738934 chr4:143738922-143738933 chr4:143738924-143738933
18	CEBPB	chr4:143647708-143647757	K562	blood:	n/a	chr4:143647716-143647729
19	CEBPB	chr4:143738321-143739857	HCT-116	colon:	n/a	chr4:143738923-143738934 chr4:143738922-143738933 chr4:143738924-143738933
20	CEBPB	chr4:143738630-143739116	IMR90	lung:	n/a	chr4:143738923-143738934 chr4:143738922-143738933 chr4:143738924-143738933
21	CEBPB	chr4:143737033-143737390	IMR90	lung:	n/a	n/a
22	CEBPB	chr4:143664206-143664406	A549	lung:	n/a	chr4:143664319-143664330
23	CEBPB	chr4:143844878-143845386	MCF-7	breast:	n/a	chr4:143845173-143845186
24	CEBPB	chr4:143699270-143699405	IMR90	lung:	n/a	n/a
25	CEBPB	chr4:143664214-143664470	HepG2	liver:	n/a	chr4:143664319-143664330
26	CEBPB	chr4:143664141-143664514	IMR90	lung:	n/a	chr4:143664319-143664330
27	CEBPB	chr4:143737008-143737347	Hela-S3	cervix:	n/a	n/a
28	CEBPB	chr4:143652977-143653126	H1-hESC	embryonic stem cell:	n/a	n/a
29	CEBPB	chr4:143765458-143765738	A549	lung:	n/a	chr4:143765553-143765566
30	CEBPB	chr4:143738590-143739134	Hela-S3	cervix:	n/a	chr4:143738923-143738934 chr4:143738922-143738933 chr4:143738924-143738933
31	CEBPB	chr4:143796747-143797030	HepG2	liver:	n/a	chr4:143796857-143796868
32	CEBPB	chr4:143732978-143733184	A549	lung:	n/a	n/a
33	CEBPB	chr4:143698743-143698867	A549	lung:	n/a	n/a
34	CHD2	chr4:143738570-143738994	Hela-S3	cervix:	n/a	n/a
35	CHD2	chr4:143768391-143768792	Hela-S3	cervix:	n/a	n/a
36	CHD2	chr4:143768468-143768600	GM12878	blood:	n/a	n/a
37	CHD2	chr4:143767470-143767862	Hela-S3	cervix:	n/a	n/a
38	CTCF	chr4:143663245-143663484	MCF-7	breast:	n/a	n/a
39	CTCF	chr4:143771722-143771920	HUVEC	blood vessel:	n/a	n/a
40	CTCF	chr4:143641400-143641550	HPAF	blood vessel:	n/a	chr4:143641490-143641511 chr4:143641496-143641512 chr4:143641495-143641513
41	CTCF	chr4:143663256-143663436	LNCaP	prostate:	n/a	n/a
42	CTCF	chr4:143771742-143771870	HepG2	liver:	n/a	n/a
43	CTCF	chr4:143663300-143663450	SAEC	small airway:	n/a	n/a
44	CTCF	chr4:143804760-143804910	HUVEC	blood vessel:	n/a	chr4:143804776-143804797 chr4:143804774-143804792
45	CTCF	chr4:143641420-143641570	WERI-Rb-1	eye:	n/a	chr4:143641490-143641511 chr4:143641496-143641512 chr4:143641495-143641513
46	CTCF	chr4:143771797-143771856	NHEK	skin:	n/a	n/a
47	CTCF	chr4:143804660-143804810	SAEC	small airway:	n/a	chr4:143804776-143804797 chr4:143804774-143804792
48	CTCF	chr4:143838978-143839083	GM12878	blood:	n/a	n/a
49	CTCF	chr4:143804700-143804850	Caco-2	colon:	n/a	chr4:143804776-143804797 chr4:143804774-143804792
50	CTCF	chr4:143771680-143771930	GM12872	blood:	n/a	n/a

(count:1221 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:143754306-143754356	HEK293	kidney:	embryo
2	chr4:143754306-143754356	HEK293	kidney:	embryo
3	chr4:143776422-143776472	Hepatocyte	liver:	n/a
4	chr4:143767645-143767695	Hela-S3	cervix:	n/a
5	chr4:143771325-143771375	NH-A	brain:	n/a
6	chr4:143767621-143767671	ECC-1	luminal epithelium:	n/a
7	chr4:143767118-143767168	MCF-7	breast:	n/a
8	chr4:143766916-143766966	ovcar-3	ovarian:	n/a
9	chr4:143767118-143767168	HEK293	kidney:	embryo
10	chr4:143767118-143767168	IMR90	lung:	fetal
11	chr4:143767118-143767168	HIPEpiC	eye:	n/a
12	chr4:143767647-143767697	HNPCEpiC	eye:	n/a
13	chr4:143766602-143766652	HCM	heart:	n/a
14	chr4:143754306-143754356	AG10803	skin:	n/a
15	chr4:143767621-143767671	HCT-116	colon:	n/a
16	chr4:143768727-143768777	GM19239	blood:	n/a
17	chr4:143767608-143767658	NB4	blood:	n/a
18	chr4:143776422-143776472	HEEpiC	esophagus:	n/a
19	chr4:143767424-143767474	NT2-D1	testis:	n/a
20	chr4:143767672-143767722	ECC-1	luminal epithelium:	n/a
21	chr4:143768134-143768184	HUVEC	blood vessel:	n/a
22	chr4:143748032-143748082	T-47D	breast:	n/a
23	chr4:143748032-143748082	HIPEpiC	eye:	n/a
24	chr4:143768134-143768184	T-47D	breast:	n/a
25	chr4:143767647-143767697	HIPEpiC	eye:	n/a
26	chr4:143748032-143748082	MCF-7	breast:	n/a
27	chr4:143767608-143767658	AG04449	skin:	fetal
28	chr4:143766916-143766966	HAEpiC	amniotic membrane:	n/a
29	chr4:143765657-143765707	IMR90	lung:	fetal
30	chr4:143767454-143767504	HRCEpiC	kidney:	n/a
31	chr4:143767645-143767695	AoSMC	blood vessel:	n/a
32	chr4:143754306-143754356	HRCEpiC	kidney:	n/a
33	chr4:143754306-143754356	K562	blood:	n/a
34	chr4:143767424-143767474	Hepatocyte	liver:	n/a
35	chr4:143767645-143767695	AG04450	lung:	fetal
36	chr4:143819041-143819091	NT2-D1	testis:	n/a
37	chr4:143766916-143766966	GM19239	blood:	n/a
38	chr4:143766916-143766966	HIPEpiC	eye:	n/a
39	chr4:143767670-143767720	SK-N-SH	brain:	n/a
40	chr4:143768275-143768325	A549	lung:	n/a
41	chr4:143767647-143767697	Caco-2	colon:	n/a
42	chr4:143766916-143766966	AG04450	lung:	fetal
43	chr4:143765657-143765707	HCT-116	colon:	n/a
44	chr4:143767454-143767504	NT2-D1	testis:	n/a
45	chr4:143767645-143767695	AG09319	gingival:	n/a
46	chr4:143765657-143765707	HEK293	kidney:	embryo
47	chr4:143767608-143767658	HMEC	breast:	n/a
48	chr4:143768134-143768184	BE2_C	brain:	n/a
49	chr4:143768134-143768184	HEEpiC	esophagus:	n/a
50	chr4:143765657-143765707	NT2-D1	testis:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr4:143391120..143394953-chr4:143764140..143771077,8	MCF-7	breast:
2	chr4:143767768..143770227-chr4:143771801..143773532,2	MCF-7	breast:
3	chr4:143804340..143805239-chr4:143946331..143947512,3	MCF-7	breast:
4	chr4:143757278..143761783-chr4:143763336..143768943,6	MCF-7	breast:
5	chr4:143393242..143395860-chr4:143757386..143759845,3	MCF-7	breast:
6	chr4:143401960..143404960-chr4:143637401..143640738,3	MCF-7	breast:
7	chr4:143393131..143399799-chr4:143636317..143645681,15	MCF-7	breast:
8	chr4:143845292..143846837-chr4:143847161..143849163,2	MCF-7	breast:
9	chr4:143724161..143726942-chr4:143730485..143732877,2	K562	blood:
10	chr4:143728789..143731644-chr4:143731660..143733720,2	MCF-7	breast:
11	chr4:143762270..143764702-chr4:143766052..143770313,5	MCF-7	breast:
12	chr4:143394255..143395855-chr4:143697810..143700529,2	MCF-7	breast:
13	chr4:143536517..143538495-chr4:143637512..143640289,2	MCF-7	breast:
14	chr4:143766691..143769165-chr4:143778080..143780463,3	MCF-7	breast:
15	chr4:143651955..143654079-chr4:143655734..143658142,2	MCF-7	breast:
16	chr4:143847589..143849714-chr4:144104307..144107096,2	K562	blood:
17	chr4:143651955..143654079-chr4:143655734..143658142,2	MCF-7	breast:
18	chr4:143740384..143741938-chr4:143748371..143749871,2	MCF-7	breast:
19	chr4:143381634..143384495-chr4:143762183..143764564,2	MCF-7	breast:
20	chr4:143771733..143772322-chr4:143906005..143906508,2	MCF-7	breast:
21	chr4:143804603..143805356-chr4:144006149..144006825,3	MCF-7	breast:
22	chr4:143637297..143639595-chr4:143640905..143643324,3	MCF-7	breast:
23	chr4:143391122..143393717-chr4:143678959..143680972,2	MCF-7	breast:
24	chr4:143637297..143639595-chr4:143640905..143643324,3	MCF-7	breast:
25	chr4:143845292..143846837-chr4:143847161..143849163,2	MCF-7	breast:
26	chr4:143653633..143656587-chr4:143659661..143662244,2	MCF-7	breast:
27	chr4:143740384..143741938-chr4:143748371..143749871,2	MCF-7	breast:
28	chr4:142782252..142782833-chr4:143767690..143768206,2	MCF-7	breast:
29	chr4:143395153..143399388-chr4:143754064..143757288,4	MCF-7	breast:
30	chr4:143728789..143731644-chr4:143731660..143733720,2	MCF-7	breast:
31	chr4:143795116..143796880-chr4:143868819..143870461,2	MCF-7	breast:
32	chr4:143392644..143398601-chr4:143638137..143645320,14	MCF-7	breast:
33	chr4:143395579..143398506-chr4:143758143..143759826,2	MCF-7	breast:
34	chr4:143764792..143768376-chr4:144104488..144107848,3	MCF-7	breast:
35	chr4:143391004..143397300-chr4:143759915..143764343,9	MCF-7	breast:
36	chr4:143470482..143472862-chr4:143765653..143767436,2	MCF-7	breast:
37	chr4:143535273..143539133-chr4:143641663..143644812,3	MCF-7	breast:
38	chr4:143562963..143564515-chr4:143746761..143748551,2	MCF-7	breast:
39	chr4:143741827..143744468-chr4:143744792..143746567,2	MCF-7	breast:
40	chr4:143682400..143684805-chr4:143686793..143689462,3	K562	blood:
41	chr4:143644944..143646737-chr4:143768301..143769914,2	MCF-7	breast:
42	chr4:143392966..143400087-chr4:143764739..143770446,12	MCF-7	breast:
43	chr4:143634044..143636846-chr4:143637396..143641073,3	MCF-7	breast:
44	chr4:143728679..143731015-chr4:143735952..143738151,2	MCF-7	breast:
45	chr4:143653633..143656587-chr4:143659661..143662244,2	MCF-7	breast:
46	chr4:143646473..143648911-chr4:143650261..143652367,2	MCF-7	breast:
47	chr4:143724161..143726942-chr4:143730485..143732877,2	K562	blood:
48	chr4:143803402..143804305-chr4:143946373..143947084,2	MCF-7	breast:
49	chr4:143646473..143648911-chr4:143650261..143652367,2	MCF-7	breast:
50	chr4:143777512..143779890-chr4:144104610..144106802,2	MCF-7	breast:

(count:14 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FREM3-8	chr4:143688742-143688814	NONHSAT098540
2	lnc-FREM3-8	chr4:143687891-143687990	NONHSAT098541
3	lnc-FREM3-7	chr4:143716305-143716766	NONHSAT098542
4	lnc-FREM3-7	chr4:143767362-143767484	NONHSAT098542
5	lnc-INPP4B-1	chr4:143839745-143839844	XLOC_004105
6	lnc-INPP4B-1	chr4:143837531-143837941	XLOC_004105
7	lnc-FREM3-8	chr4:143687891-143688005	NONHSAT098540
8	lnc-FREM3-8	chr4:143688985-143689122	NONHSAT098541
9	lnc-FREM3-8	chr4:143687027-143687156	NONHSAT098540
10	lnc-FREM3-8	chr4:143646992-143647054	NONHSAT098539
11	lnc-USP38-1	chr4:143778385-143778965	XLOC_003714
12	lnc-USP38-1	chr4:143772645-143772804	XLOC_003714
13	lnc-FREM3-8	chr4:143688985-143689007	NONHSAT098540
14	lnc-FREM3-8	chr4:143687891-143687972	NONHSAT098539

No data

Variant related genes	Relation type
INPP4B	TF binding region
INPP4B	CpG island
ENSG00000109452	chromatin interactions
ENSG00000170185	chromatin interactions
ENSG00000250326	chromatin interactions
NR3C2	miRNA target sites
RNF141	miRNA target sites

Extended variants
information (count: 6614 )
Associated
traits (count: 74 )

Variant overlapped rSNPs/rCNVs (count:6614 , 50 per page) page: 1 2 3 4 5 6 7 ... 133

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4690699	chr4:143639498-143639499	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs567994191	chr4:143639508-143639509	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs552061727	chr4:143639510-143639511	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs192788651	chr4:143639527-143639528	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs72728621	chr4:143639585-143639586	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs553799817	chr4:143639586-143639587	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs560803509	chr4:143639592-143639593	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs373646960	chr4:143639626-143639627	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs565928395	chr4:143639649-143639650	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs377388639	chr4:143639667-143639668	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs61289420	chr4:143639675-143639676	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs142630876	chr4:143639676-143639677	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs533361317	chr4:143639722-143639723	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs571259027	chr4:143639723-143639724	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs558031447	chr4:143639734-143639735	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs532420633	chr4:143639739-143639740	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs572449506	chr4:143639759-143639760	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs533920748	chr4:143639760-143639761	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs576295245	chr4:143639779-143639780	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs555767472	chr4:143639796-143639797	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs567568105	chr4:143639990-143639991	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs80115452	chr4:143639995-143639996	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs183795676	chr4:143640048-143640049	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs189258518	chr4:143640051-143640052	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs150981740	chr4:143640122-143640123	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs554085014	chr4:143640134-143640135	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs543969264	chr4:143640160-143640161	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs542571024	chr4:143640173-143640174	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs192058091	chr4:143640201-143640202	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs531208444	chr4:143640203-143640204	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs543467800	chr4:143640243-143640244	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs576818133	chr4:143640350-143640351	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs111341535	chr4:143640360-143640361	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs564682348	chr4:143640374-143640375	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs1373032	chr4:143640523-143640524	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs551588914	chr4:143640533-143640534	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs573966216	chr4:143640546-143640547	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs114736485	chr4:143640563-143640564	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs184201760	chr4:143640570-143640571	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs567605245	chr4:143640615-143640616	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs13135210	chr4:143640624-143640625	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs567593115	chr4:143640625-143640626	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs188953816	chr4:143640627-143640628	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs538819457	chr4:143640634-143640635	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs553972971	chr4:143640661-143640662	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs551016035	chr4:143640705-143640706	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs374182644	chr4:143640709-143640710	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs28369300	chr4:143640713-143640714	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs146067533	chr4:143640717-143640718	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs147774128	chr4:143640724-143640725	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:74)

Disease	PMID	Source
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Medulloblastoma	21979893	CNVD
Neuroblastoma	18923191	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	21858162	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Colorectal cancer	19359472	CNVD
Malignant mesothelioma	18160781	CNVD
Medulloblastoma	18056178	CNVD
Multiple myeloma	17077331	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Oral squamous cell carcinoma	17134496	CNVD
4q-syndrome	17576883	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Muscular dystrophy	21149563	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Cervical cancer	21062161	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	16608533	CNVD
Lung cancer	19208797	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21785460	CNVD
Lung cancer	18438408	CNVD
Cancer	22429812	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	21183584	CNVD
primary effusion lymphomas	17116491	CNVD
Breast cancer	16272173	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17133270	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Congenital anomalies of the kidney and urinary tract	20505237	CNVD
Breast cancer	17393978	CNVD
Esophageal cancer	21851588	CNVD
Testicular germ cell tumor	18059402	CNVD
Ovarian cancer	22174824	CNVD
Olfactory neuroblastoma	18408657	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Mental retardation	17901693	CNVD
small cell lung cancer	20016488	CNVD
Developmental delay	21147756	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Myelofibrosis	22110671	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Ewing''s sarcoma	17952124	CNVD
Obesity	20622171	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Breast cancer	22048815	CNVD
Autism	22241247	CNVD
Glioblastoma multiforme	22286061	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1158 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:143620800-143642000	Weak transcription	Fetal Heart	heart
2	chr4:143625200-143641600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr4:143630200-143640600	Weak transcription	Primary T cells fromperipheralblood	blood
4	chr4:143630800-143650200	Weak transcription	Aorta	Aorta
5	chr4:143632400-143640200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
6	chr4:143635000-143648200	Weak transcription	Thymus	Thymus
7	chr4:143635600-143641000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
8	chr4:143636200-143640000	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
9	chr4:143636400-143639600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
10	chr4:143636400-143641000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
11	chr4:143636600-143639800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
12	chr4:143636600-143641000	Weak transcription	Primary T cells from cord blood	blood
13	chr4:143636800-143639600	Weak transcription	Dnd41	blood
14	chr4:143637200-143653000	Weak transcription	Left Ventricle	heart
15	chr4:143637400-143640200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
16	chr4:143637400-143640600	Weak transcription	Primary hematopoietic stem cells	blood
17	chr4:143637800-143641000	Weak transcription	Primary T helper cells fromperipheralblood	blood
18	chr4:143639200-143641800	Enhancers	Primary T helper cells PMA-I stimulated	--
19	chr4:143639400-143640200	Enhancers	Primary T helper naive cells from peripheral blood	blood
20	chr4:143639600-143641400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
21	chr4:143639600-143641600	Enhancers	Primary T helper naive cells fromperipheralblood	blood
22	chr4:143639600-143647000	Enhancers	Dnd41	blood
23	chr4:143639800-143640400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
24	chr4:143640000-143641200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
25	chr4:143640000-143641400	Enhancers	Primary T regulatory cells fromperipheralblood	blood
26	chr4:143640200-143641000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
27	chr4:143640200-143641000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
28	chr4:143640200-143641400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
29	chr4:143640200-143641800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
30	chr4:143640200-143642200	Enhancers	NHEK	skin
31	chr4:143640200-143642800	Enhancers	HMEC	breast
32	chr4:143640400-143640800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
33	chr4:143640600-143640800	Enhancers	Primary T cells fromperipheralblood	blood
34	chr4:143640600-143641600	Enhancers	Primary hematopoietic stem cells	blood
35	chr4:143640800-143641400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
36	chr4:143641000-143641200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
37	chr4:143641000-143641200	Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
38	chr4:143641000-143641400	Enhancers	Primary T cells from cord blood	blood
39	chr4:143641000-143641400	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
40	chr4:143641000-143641400	Enhancers	Primary T helper cells fromperipheralblood	blood
41	chr4:143641000-143641400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
42	chr4:143641000-143641400	Enhancers	Pancreatic Islets	Pancreatic Islet
43	chr4:143641000-143641400	Enhancers	NHDF-Ad	bronchial
44	chr4:143641000-143641400	Enhancers	Osteobl	bone
45	chr4:143641000-143641800	Enhancers	Primary T helper naive cells from peripheral blood	blood
46	chr4:143641000-143641800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
47	chr4:143641000-143642600	Enhancers	Muscle Satellite Cultured Cells	--
48	chr4:143641000-143642600	Enhancers	NH-A	brain
49	chr4:143641200-143641400	Flanking Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
50	chr4:143641200-143641600	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin

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