Variant report

Variant	nsv879920
Chromosome Location	chr4:128554404-128694288
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:885)
CpG islands
(count:977)
Chromatin interactive
region (count:59)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:885 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:128653832-128654129	K562	blood:	n/a	n/a
2	ARID3A	chr4:128553939-128554513	HepG2	liver:	n/a	n/a
3	ARID3A	chr4:128658272-128658704	K562	blood:	n/a	n/a
4	ARID3A	chr4:128681078-128681272	HepG2	liver:	n/a	n/a
5	ARID3A	chr4:128692810-128693068	K562	blood:	n/a	n/a
6	ATF1	chr4:128692637-128692941	K562	blood:	n/a	n/a
7	ATF1	chr4:128653837-128654173	K562	blood:	n/a	n/a
8	ATF2	chr4:128619722-128620294	GM12878	blood:	n/a	n/a
9	ATF2	chr4:128619738-128620345	GM12878	blood:	n/a	n/a
10	ATF3	chr4:128619938-128620425	HCT-116	colon:	n/a	n/a
11	ATF3	chr4:128670080-128670482	K562	blood:	n/a	n/a
12	ATF3	chr4:128651355-128651575	K562	blood:	n/a	chr4:128651557-128651566
13	BATF	chr4:128619897-128620328	GM12878	blood:	n/a	n/a
14	BATF	chr4:128619916-128620358	GM12878	blood:	n/a	n/a
15	BCL11A	chr4:128619905-128620297	GM12878	blood:	n/a	n/a
16	BCL11A	chr4:128619778-128620281	GM12878	blood:	n/a	n/a
17	BCL3	chr4:128619800-128620319	GM12878	blood:	n/a	n/a
18	BCLAF1	chr4:128619855-128620353	GM12878	blood:	n/a	n/a
19	BCLAF1	chr4:128619765-128620391	GM12878	blood:	n/a	n/a
20	BHLHE40	chr4:128608804-128608829	K562	blood:	n/a	n/a
21	BHLHE40	chr4:128619830-128620287	GM12878	blood:	n/a	n/a
22	BHLHE40	chr4:128556123-128556195	K562	blood:	n/a	n/a
23	BHLHE40	chr4:128555081-128555088	GM12878	blood:	n/a	n/a
24	BHLHE40	chr4:128651381-128651572	K562	blood:	n/a	n/a
25	CBX3	chr4:128619927-128620413	HCT-116	colon:	n/a	n/a
26	CBX3	chr4:128629996-128630593	HCT-116	colon:	n/a	n/a
27	CBX3	chr4:128670109-128670502	K562	blood:	n/a	n/a
28	CBX3	chr4:128663246-128663643	K562	blood:	n/a	n/a
29	CBX3	chr4:128619911-128620372	HCT-116	colon:	n/a	n/a
30	CBX3	chr4:128670168-128670534	HCT-116	colon:	n/a	n/a
31	CBX3	chr4:128670087-128670514	K562	blood:	n/a	n/a
32	CBX3	chr4:128629998-128630740	HCT-116	colon:	n/a	n/a
33	CEBPB	chr4:128620085-128620432	A549	lung:	n/a	chr4:128620151-128620164
34	CEBPB	chr4:128670199-128670501	H1-hESC	embryonic stem cell:	n/a	n/a
35	CEBPB	chr4:128567258-128567458	HepG2	liver:	n/a	chr4:128567371-128567382
36	CEBPB	chr4:128619959-128620538	A549	lung:	n/a	chr4:128620151-128620164
37	CEBPB	chr4:128670033-128670574	HCT-116	colon:	n/a	n/a
38	CEBPB	chr4:128620165-128620873	K562	blood:	n/a	n/a
39	CEBPB	chr4:128656194-128656400	A549	lung:	n/a	n/a
40	CEBPB	chr4:128686132-128686276	HepG2	liver:	n/a	chr4:128686203-128686214
41	CEBPB	chr4:128563364-128563736	IMR90	lung:	n/a	n/a
42	CEBPB	chr4:128607797-128608186	Hela-S3	cervix:	n/a	n/a
43	CEBPB	chr4:128630125-128630810	Hela-S3	cervix:	n/a	n/a
44	CEBPB	chr4:128670126-128670518	K562	blood:	n/a	n/a
45	CEBPB	chr4:128567305-128567505	IMR90	lung:	n/a	chr4:128567371-128567382
46	CEBPB	chr4:128619883-128620426	GM12878	blood:	n/a	chr4:128620151-128620164
47	CEBPB	chr4:128619793-128620638	HCT-116	colon:	n/a	chr4:128620151-128620164
48	CEBPB	chr4:128670104-128670474	K562	blood:	n/a	n/a
49	CEBPB	chr4:128619803-128620583	HCT-116	colon:	n/a	chr4:128620151-128620164
50	CEBPB	chr4:128620014-128620810	IMR90	lung:	n/a	chr4:128620151-128620164

(count:977 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:128630266-128630316	AG09309	skin:	n/a
2	chr4:128630266-128630316	AG09309	skin:	n/a
3	chr4:128630266-128630316	HPAEpiC	pulmonary alveolar:	n/a
4	chr4:128651221-128651271	SK-N-MC	brain:	n/a
5	chr4:128647957-128648007	SK-N-MC	brain:	n/a
6	chr4:128650828-128650878	MCF10A-Er-Src	breast:	n/a
7	chr4:128651518-128651568	RPTEC	kidney:	n/a
8	chr4:128651532-128651582	SAEC	small airway:	n/a
9	chr4:128651936-128651986	HCPEpiC	choroid plexus:	n/a
10	chr4:128651936-128651986	SAEC	small airway:	n/a
11	chr4:128651500-128651550	ovcar-3	ovarian:	n/a
12	chr4:128650828-128650878	HCM	heart:	n/a
13	chr4:128637608-128637658	K562	blood:	n/a
14	chr4:128650828-128650878	AG04449	skin:	fetal
15	chr4:128651564-128651614	A549	lung:	n/a
16	chr4:128651221-128651271	ECC-1	luminal epithelium:	n/a
17	chr4:128651936-128651986	HEEpiC	esophagus:	n/a
18	chr4:128654094-128654144	SK-N-SH_RA	brain:	n/a
19	chr4:128651221-128651271	GM12878	blood:	n/a
20	chr4:128651564-128651614	HL-60	blood:	n/a
21	chr4:128637608-128637658	HepG2	liver:	n/a
22	chr4:128651543-128651593	U87	brain:	n/a
23	chr4:128650828-128650878	NHBE	bronchial:	n/a
24	chr4:128651526-128651576	HCF	heart:	n/a
25	chr4:128650828-128650878	GM19239	blood:	n/a
26	chr4:128651221-128651271	LNCaP	prostate:	n/a
27	chr4:128647957-128648007	HCPEpiC	choroid plexus:	n/a
28	chr4:128651564-128651614	HAEpiC	amniotic membrane:	n/a
29	chr4:128647957-128648007	A549	lung:	n/a
30	chr4:128654094-128654144	T-47D	breast:	n/a
31	chr4:128651526-128651576	ECC-1	luminal epithelium:	n/a
32	chr4:128651500-128651550	HL-60	blood:	n/a
33	chr4:128651500-128651550	HRCEpiC	kidney:	n/a
34	chr4:128630266-128630316	SKMC	muscle:	n/a
35	chr4:128651564-128651614	ECC-1	luminal epithelium:	n/a
36	chr4:128637608-128637658	NHBE	bronchial:	n/a
37	chr4:128651206-128651256	SK-N-SH	brain:	n/a
38	chr4:128650828-128650878	HUVEC	blood vessel:	n/a
39	chr4:128651936-128651986	HPAEpiC	pulmonary alveolar:	n/a
40	chr4:128651543-128651593	HRE	kidney:	n/a
41	chr4:128651707-128651757	AoSMC	blood vessel:	n/a
42	chr4:128654094-128654144	GM12891	blood:	n/a
43	chr4:128651206-128651256	NT2-D1	testis:	n/a
44	chr4:128630266-128630316	SAEC	small airway:	n/a
45	chr4:128651206-128651256	AG10803	skin:	n/a
46	chr4:128651532-128651582	HRE	kidney:	n/a
47	chr4:128651564-128651614	GM06990	blood:	n/a
48	chr4:128651936-128651986	GM06990	blood:	n/a
49	chr4:128651543-128651593	CMK	blood:	n/a
50	chr4:128651206-128651256	Hepatocyte	liver:	n/a

(count:59 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr4:128577312..128579326-chr4:128581308..128583694,3	K562	blood:
2	chr4:128653835..128656903-chr4:128701461..128704105,3	K562	blood:
3	chr4:128555533..128557776-chr4:128702998..128704623,2	K562	blood:
4	chr4:128522468..128525015-chr4:128578213..128580607,2	K562	blood:
5	chr4:128552130..128555058-chr4:128565621..128568955,3	MCF-7	breast:
6	chr4:128580018..128583364-chr4:128583861..128587537,3	K562	blood:
7	chr4:128564328..128566993-chr4:128568354..128570269,2	MCF-7	breast:
8	chr4:128609167..128611494-chr4:128612179..128614803,2	K562	blood:
9	chr4:128691903..128693530-chr4:128709934..128712766,2	K562	blood:
10	chr4:128576214..128579194-chr4:128579310..128580925,2	K562	blood:
11	chr4:128689601..128691361-chr4:128702000..128704848,2	K562	blood:
12	chr4:128525423..128527600-chr4:128653005..128654534,14	MCF-7	breast:
13	chr4:128651856..128654321-chr4:128662379..128665043,2	K562	blood:
14	chr4:128553197..128555974-chr4:128981706..128984336,2	K562	blood:
15	chr4:128558656..128560613-chr4:128567369..128568962,2	K562	blood:
16	chr4:128620470..128623327-chr4:128629151..128632115,2	K562	blood:
17	chr4:128590271..128592310-chr4:128594273..128597099,2	K562	blood:
18	chr4:128651856..128654321-chr4:128662379..128665043,2	K562	blood:
19	chr4:128552418..128557041-chr4:128564673..128569925,6	K562	blood:
20	chr4:128534491..128537175-chr4:128554257..128557179,2	MCF-7	breast:
21	chr4:128542741..128545143-chr4:128558778..128561297,2	MCF-7	breast:
22	chr4:128666387..128668298-chr4:128668505..128671466,2	K562	blood:
23	chr4:128657662..128659612-chr4:128665725..128667631,2	K562	blood:
24	chr4:128543078..128545882-chr4:128552977..128554729,2	MCF-7	breast:
25	chr4:128552732..128556241-chr4:128556449..128559668,4	K562	blood:
26	chr4:128575980..128578984-chr4:128579310..128583606,5	K562	blood:
27	chr4:128577312..128579326-chr4:128581308..128583694,3	K562	blood:
28	chr4:128580018..128583364-chr4:128583861..128587537,3	K562	blood:
29	chr4:128564328..128566993-chr4:128568354..128570269,2	MCF-7	breast:
30	chr4:128581030..128583943-chr4:128656313..128658380,2	K562	blood:
31	chr4:128553083..128556117-chr4:128559981..128561988,3	K562	blood:
32	chr4:128684085..128685592-chr4:128688518..128690302,2	K562	blood:
33	chr4:128552432..128554682-chr4:128586410..128589274,2	K562	blood:
34	chr4:128526494..128527032-chr4:128651880..128652572,2	MCF-7	breast:
35	chr4:128684085..128685592-chr4:128688518..128690302,2	K562	blood:
36	chr4:128552219..128554682-chr4:128585825..128589274,3	K562	blood:
37	chr4:128609167..128611494-chr4:128612179..128614803,2	K562	blood:
38	chr4:128666387..128668298-chr4:128668505..128671466,2	K562	blood:
39	chr4:128581030..128583943-chr4:128656313..128658380,2	K562	blood:
40	chr4:128553083..128555674-chr4:128560007..128562202,4	K562	blood:
41	chr4:128561660..128563498-chr4:128564714..128566263,2	MCF-7	breast:
42	chr4:128553241..128556204-chr4:128562261..128565320,4	K562	blood:
43	chr4:128575980..128578984-chr4:128579310..128583606,5	K562	blood:
44	chr4:128525866..128527137-chr4:128653218..128654151,10	K562	blood:
45	chr4:128684329..128686101-chr4:128689330..128691100,2	MCF-7	breast:
46	chr1:174967985..174968897-chr4:128553828..128554517,2	Hela-S3	cervix:
47	chr4:128587279..128589400-chr4:128808635..128811454,2	K562	blood:
48	chr4:128576214..128579194-chr4:128579310..128580925,2	K562	blood:
49	chr4:128521727..128523968-chr4:128577085..128579713,2	K562	blood:
50	chr4:128684329..128686101-chr4:128689330..128691100,2	MCF-7	breast:

(count:3 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SLC25A31-3	chr4:128595309-128595368	NONHSAT098240
2	lnc-SLC25A31-3	chr4:128606597-128607105	NONHSAT098240
3	lnc-SLC25A31-3	chr4:128605564-128605641	NONHSAT098240

No data

Variant related genes	Relation type
SLC25A31	TF binding region
INTU	TF binding region
SLC25A31	CpG island
INTU	CpG island
ENSG00000164066	chromatin interactions
ENSG00000164070	chromatin interactions
ENSG00000116161	chromatin interactions
ENSG00000138709	chromatin interactions

Extended variants
information (count: 4024 )
Associated
traits (count: 72 )

Variant overlapped rSNPs/rCNVs (count:4024 , 50 per page) page: 1 2 3 4 5 6 7 ... 81

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2255457	chr4:128554404-128554405	Active TSS Flanking Active TSS Bivalent/Poised TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs377700399	chr4:128554433-128554434	Active TSS Flanking Active TSS Bivalent/Poised TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs528887434	chr4:128554434-128554435	Active TSS Flanking Active TSS Bivalent/Poised TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs547427317	chr4:128554443-128554444	Active TSS Flanking Active TSS Bivalent/Poised TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs376480510	chr4:128554447-128554448	Active TSS Flanking Active TSS Bivalent/Poised TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs565735369	chr4:128554515-128554516	Active TSS Flanking Active TSS Bivalent/Poised TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs532908626	chr4:128554622-128554623	Active TSS Flanking Active TSS Enhancers Bivalent Enhancer Bivalent/Poised TSS Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs551521711	chr4:128554644-128554645	Active TSS Flanking Active TSS Enhancers Bivalent Enhancer Bivalent/Poised TSS Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs569727569	chr4:128554645-128554646	Active TSS Flanking Active TSS Enhancers Bivalent Enhancer Bivalent/Poised TSS Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs537297398	chr4:128554665-128554666	Active TSS Flanking Active TSS Enhancers Bivalent Enhancer Bivalent/Poised TSS Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs555230906	chr4:128554669-128554670	Active TSS Flanking Active TSS Enhancers Bivalent Enhancer Bivalent/Poised TSS Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs567230388	chr4:128554708-128554709	Active TSS Flanking Active TSS Enhancers Bivalent Enhancer Bivalent/Poised TSS Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs568947727	chr4:128554736-128554737	Active TSS Flanking Active TSS Enhancers Bivalent Enhancer Bivalent/Poised TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs80342004	chr4:128554825-128554826	Active TSS Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs553771655	chr4:128554848-128554849	Active TSS Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs572467607	chr4:128554888-128554889	Active TSS Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs72624504	chr4:128554952-128554953	Active TSS Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs189689076	chr4:128554983-128554984	Active TSS Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs181025875	chr4:128555014-128555015	Active TSS Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs535948010	chr4:128555053-128555054	Active TSS Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs554167955	chr4:128555066-128555067	Active TSS Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs373558640	chr4:128555067-128555068	Active TSS Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs544035598	chr4:128555186-128555187	Active TSS Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs552441807	chr4:128555288-128555289	Weak transcription Flanking Active TSS Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs562331252	chr4:128555305-128555306	Weak transcription Flanking Active TSS Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs142254344	chr4:128555328-128555329	Weak transcription Flanking Active TSS Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs541000404	chr4:128555329-128555330	Weak transcription Flanking Active TSS Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs559409331	chr4:128555346-128555347	Weak transcription Flanking Active TSS Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs367739327	chr4:128555362-128555363	Weak transcription Flanking Active TSS Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs532969701	chr4:128555415-128555416	Weak transcription Flanking Active TSS Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs10009032	chr4:128555418-128555419	Weak transcription Flanking Active TSS Active TSS Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs201603470	chr4:128555467-128555468	Weak transcription Flanking Active TSS Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs72624505	chr4:128555469-128555470	Weak transcription Flanking Active TSS Active TSS Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs548768567	chr4:128555494-128555495	Weak transcription Flanking Active TSS Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs185288698	chr4:128555613-128555614	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs534617477	chr4:128555684-128555685	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs151250210	chr4:128555701-128555702	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs140473667	chr4:128555724-128555725	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs539870003	chr4:128555780-128555781	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs143058522	chr4:128555781-128555782	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs73847023	chr4:128555820-128555821	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs576491303	chr4:128555827-128555828	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs138144693	chr4:128555857-128555858	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs368786084	chr4:128555858-128555859	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs537597249	chr4:128555889-128555890	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs556020784	chr4:128555920-128555921	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs190150807	chr4:128555934-128555935	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs368133597	chr4:128556024-128556025	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs541733285	chr4:128556070-128556071	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs6836676	chr4:128556242-128556243	Weak transcription Active TSS Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:72)

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
Thoracic aortic aneurysm	21092924	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
Breast cancer	16272173	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
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17133270	CNVD
Colorectal cancer	20459617	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
Colorectal cancer	16272173	CNVD
Testicular germ cell tumor	18059402	CNVD
Ovarian cancer	22174824	CNVD
Neuroblastoma	21899760	CNVD
Renal cell carcinoma	18194544	CNVD
Olfactory neuroblastoma	18408657	CNVD
Developmental delay	21147756	CNVD
Renal cell carcinoma	18765545	CNVD
Hepatocellular carcinoma	16750200	CNVD
Myelofibrosis	22110671	CNVD
Acute myeloid leukemia	16864856	CNVD
Hodgkin''s lymphoma	18641027	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1394 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:128553000-128554800	Active TSS	Pancreatic Islets	Pancreatic Islet
2	chr4:128553000-128555200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
3	chr4:128553200-128554800	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
4	chr4:128553200-128555400	Active TSS	HUES48 Cell Line	embryonic stem cell
5	chr4:128553200-128555800	Active TSS	iPS-20b Cell Line	embryonic stem cell
6	chr4:128553400-128554600	Active TSS	ES-WA7 Cell Line	embryonic stem cell
7	chr4:128553400-128554600	Bivalent/Poised TSS	Primary B cells from cord blood	blood
8	chr4:128553400-128554600	Active TSS	Fetal Heart	heart
9	chr4:128553400-128554600	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
10	chr4:128553400-128554600	Bivalent/Poised TSS	HepG2	liver
11	chr4:128553400-128554800	Active TSS	H9 Cell Line	embryonic stem cell
12	chr4:128553400-128554800	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
13	chr4:128553400-128554800	Active TSS	iPS-18 Cell Line	embryonic stem cell
14	chr4:128553400-128554800	Active TSS	Aorta	Aorta
15	chr4:128553400-128554800	Active TSS	Fetal Lung	lung
16	chr4:128553400-128554800	Active TSS	Fetal Muscle Leg	muscle
17	chr4:128553400-128554800	Active TSS	Skeletal Muscle Male	skeletal muscle
18	chr4:128553400-128554800	Active TSS	NH-A	brain
19	chr4:128553400-128555000	Active TSS	ES-I3 Cell Line	embryonic stem cell
20	chr4:128553400-128555000	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
21	chr4:128553400-128555000	Active TSS	Breast Myoepithelial Primary Cells	Breast
22	chr4:128553400-128555000	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
23	chr4:128553400-128555000	Active TSS	Brain Anterior Caudate	brain
24	chr4:128553400-128555000	Active TSS	Brain Cingulate Gyrus	brain
25	chr4:128553400-128555000	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
26	chr4:128553400-128555000	Active TSS	Brain Substantia Nigra	brain
27	chr4:128553400-128555000	Active TSS	Fetal Adrenal Gland	Adrenal Gland
28	chr4:128553400-128555000	Active TSS	Fetal Kidney	kidney
29	chr4:128553400-128555000	Active TSS	Fetal Stomach	stomach
30	chr4:128553400-128555000	Active TSS	Psoas Muscle	Psoas
31	chr4:128553400-128555000	Active TSS	Stomach Smooth Muscle	stomach
32	chr4:128553400-128555000	Active TSS	A549	lung
33	chr4:128553400-128555000	Active TSS	Hela-S3	cervix
34	chr4:128553400-128555000	Active TSS	NHDF-Ad	bronchial
35	chr4:128553400-128555200	Active TSS	H1 Cell Line	embryonic stem cell
36	chr4:128553400-128555200	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr4:128553400-128555200	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
38	chr4:128553400-128555200	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
39	chr4:128553400-128555200	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
40	chr4:128553400-128555200	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
41	chr4:128553400-128555200	Active TSS	Brain Hippocampus Middle	brain
42	chr4:128553400-128555200	Active TSS	Duodenum Mucosa	Duodenum
43	chr4:128553400-128555200	Active TSS	Duodenum Smooth Muscle	Duodenum
44	chr4:128553400-128555200	Active TSS	Fetal Intestine Large	intestine
45	chr4:128553400-128555200	Active TSS	Ovary	ovary
46	chr4:128553400-128555200	Active TSS	Rectal Mucosa Donor 29	rectum
47	chr4:128553400-128555200	Active TSS	Right Atrium	heart
48	chr4:128553400-128555200	Active TSS	NHLF	lung
49	chr4:128553400-128555600	Active TSS	HUES6 Cell Line	embryonic stem cell
50	chr4:128553400-128555600	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung

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