Variant report

Variant	nsv537203
Chromosome Location	chr4:103419352-103504042
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2167)
CpG islands
(count:976)
Chromatin interactive
region (count:137)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2167 , 50 per page) page: 1 2 3 4 5 6 7 ... 44

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:103423127-103423903	HepG2	liver:	n/a	n/a
2	ARID3A	chr4:103481283-103481344	K562	blood:	n/a	n/a
3	ARID3A	chr4:103422419-103422497	HepG2	liver:	n/a	n/a
4	ARID3A	chr4:103426031-103426436	HepG2	liver:	n/a	chr4:103426037-103426053 chr4:103426038-103426054
5	ARID3A	chr4:103425308-103425429	K562	blood:	n/a	n/a
6	ARID3A	chr4:103497012-103497331	HepG2	liver:	n/a	n/a
7	ARID3A	chr4:103423428-103423977	K562	blood:	n/a	n/a
8	ARID3A	chr4:103424393-103425266	HepG2	liver:	n/a	n/a
9	ARID3A	chr4:103435697-103436116	HepG2	liver:	n/a	n/a
10	ARID3A	chr4:103426914-103427114	HepG2	liver:	n/a	n/a
11	ATF1	chr4:103482780-103482850	K562	blood:	n/a	n/a
12	ATF1	chr4:103470052-103470119	K562	blood:	n/a	n/a
13	ATF1	chr4:103446350-103446507	K562	blood:	n/a	n/a
14	ATF2	chr4:103422336-103422605	GM12878	blood:	n/a	chr4:103422577-103422591
15	ATF2	chr4:103485364-103486250	GM12878	blood:	n/a	n/a
16	ATF2	chr4:103422176-103422703	GM12878	blood:	n/a	chr4:103422577-103422591
17	ATF2	chr4:103421662-103422167	GM12878	blood:	n/a	n/a
18	ATF2	chr4:103467584-103468353	GM12878	blood:	n/a	n/a
19	ATF2	chr4:103473953-103474364	GM12878	blood:	n/a	n/a
20	ATF2	chr4:103456290-103457324	GM12878	blood:	n/a	n/a
21	ATF2	chr4:103481194-103481741	GM12878	blood:	n/a	n/a
22	ATF2	chr4:103485318-103486080	GM12878	blood:	n/a	n/a
23	ATF2	chr4:103464118-103464690	GM12878	blood:	n/a	n/a
24	ATF2	chr4:103422951-103423653	GM12878	blood:	n/a	n/a
25	ATF2	chr4:103464116-103464637	GM12878	blood:	n/a	n/a
26	ATF2	chr4:103467707-103468230	GM12878	blood:	n/a	n/a
27	ATF2	chr4:103422841-103423891	GM12878	blood:	n/a	n/a
28	ATF2	chr4:103500846-103501584	GM12878	blood:	n/a	n/a
29	ATF2	chr4:103456394-103457222	GM12878	blood:	n/a	n/a
30	BACH1	chr4:103422903-103422972	K562	blood:	n/a	n/a
31	BACH1	chr4:103422814-103423269	H1-hESC	embryonic stem cell:	n/a	n/a
32	BATF	chr4:103464134-103464421	GM12878	blood:	n/a	n/a
33	BATF	chr4:103481241-103481524	GM12878	blood:	n/a	n/a
34	BATF	chr4:103423200-103423659	GM12878	blood:	n/a	n/a
35	BATF	chr4:103422320-103422641	GM12878	blood:	n/a	n/a
36	BATF	chr4:103467872-103468229	GM12878	blood:	n/a	n/a
37	BATF	chr4:103501706-103501943	GM12878	blood:	n/a	n/a
38	BATF	chr4:103485489-103485892	GM12878	blood:	n/a	n/a
39	BATF	chr4:103456579-103456914	GM12878	blood:	n/a	chr4:103456746-103456757 chr4:103456718-103456729
40	BATF	chr4:103448895-103449211	GM12878	blood:	n/a	n/a
41	BATF	chr4:103467775-103468215	GM12878	blood:	n/a	n/a
42	BATF	chr4:103485420-103485987	GM12878	blood:	n/a	n/a
43	BATF	chr4:103456514-103456880	GM12878	blood:	n/a	chr4:103456746-103456757 chr4:103456718-103456729
44	BATF	chr4:103464139-103464581	GM12878	blood:	n/a	n/a
45	BATF	chr4:103501677-103502000	GM12878	blood:	n/a	n/a
46	BATF	chr4:103456925-103457269	GM12878	blood:	n/a	chr4:103457135-103457145 chr4:103457131-103457141 chr4:103457130-103457141
47	BATF	chr4:103496549-103496811	GM12878	blood:	n/a	n/a
48	BATF	chr4:103484207-103484485	GM12878	blood:	n/a	chr4:103484413-103484421 chr4:103484382-103484393
49	BATF	chr4:103422394-103422574	GM12878	blood:	n/a	n/a
50	BATF	chr4:103481241-103481506	GM12878	blood:	n/a	n/a

(count:976 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:103422196-103422246	MCF-7	breast:	n/a
2	chr4:103489295-103489345	HMEC	breast:	n/a
3	chr4:103499194-103499244	AG04449	skin:	fetal
4	chr4:103475833-103475883	HEEpiC	esophagus:	n/a
5	chr4:103489295-103489345	HAEpiC	amniotic membrane:	n/a
6	chr4:103475833-103475883	PrEC	prostate:	n/a
7	chr4:103422050-103422100	AG04449	skin:	fetal
8	chr4:103422050-103422100	GM12892	blood:	n/a
9	chr4:103422974-103423024	T-47D	breast:	n/a
10	chr4:103489295-103489345	HEEpiC	esophagus:	n/a
11	chr4:103423492-103423542	AG04450	lung:	fetal
12	chr4:103422460-103422510	U87	brain:	n/a
13	chr4:103489295-103489345	BE2_C	brain:	n/a
14	chr4:103422460-103422510	GM06990	blood:	n/a
15	chr4:103489295-103489345	MCF10A-Er-Src	breast:	n/a
16	chr4:103422196-103422246	AG09319	gingival:	n/a
17	chr4:103423146-103423196	Jurkat	blood:	n/a
18	chr4:103422429-103422479	IMR90	lung:	fetal
19	chr4:103423368-103423418	PFSK-1	brain:	n/a
20	chr4:103475833-103475883	HAEpiC	amniotic membrane:	n/a
21	chr4:103422196-103422246	HAEpiC	amniotic membrane:	n/a
22	chr4:103426288-103426338	HEK293	kidney:	embryo
23	chr4:103423146-103423196	GM12878	blood:	n/a
24	chr4:103422460-103422510	MCF10A-Er-Src	breast:	n/a
25	chr4:103482058-103482108	RPTEC	kidney:	n/a
26	chr4:103423368-103423418	AG10803	skin:	n/a
27	chr4:103489295-103489345	AoSMC	blood vessel:	n/a
28	chr4:103423146-103423196	AG04449	skin:	fetal
29	chr4:103423368-103423418	PANC-1	pancreas:	n/a
30	chr4:103423368-103423418	LNCaP	prostate:	n/a
31	chr4:103423492-103423542	HPAEpiC	pulmonary alveolar:	n/a
32	chr4:103422050-103422100	LNCaP	prostate:	n/a
33	chr4:103422050-103422100	NH-A	brain:	n/a
34	chr4:103422429-103422479	HCF	heart:	n/a
35	chr4:103423368-103423418	HCF	heart:	n/a
36	chr4:103422050-103422100	HCPEpiC	choroid plexus:	n/a
37	chr4:103426288-103426338	GM12891	blood:	n/a
38	chr4:103482058-103482108	HIPEpiC	eye:	n/a
39	chr4:103475833-103475883	AG04450	lung:	fetal
40	chr4:103458703-103458753	LNCaP	prostate:	n/a
41	chr4:103422429-103422479	HNPCEpiC	eye:	n/a
42	chr4:103423146-103423196	HCM	heart:	n/a
43	chr4:103423368-103423418	U87	brain:	n/a
44	chr4:103482058-103482108	HCPEpiC	choroid plexus:	n/a
45	chr4:103458703-103458753	A549	lung:	n/a
46	chr4:103422460-103422510	SKMC	muscle:	n/a
47	chr4:103482058-103482108	SKMC	muscle:	n/a
48	chr4:103422050-103422100	SK-N-SH_RA	brain:	n/a
49	chr4:103422050-103422100	HCF	heart:	n/a
50	chr4:103426288-103426338	HepG2	liver:	n/a

(count:137 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr4:103426144..103427805-chr4:103429263..103431794,2	MCF-7	breast:
2	chr4:103438442..103440658-chr4:103444124..103446101,2	MCF-7	breast:
3	chr4:103351901..103354156-chr4:103421461..103424407,3	MCF-7	breast:
4	chr4:103439093..103441146-chr4:103445747..103447716,2	MCF-7	breast:
5	chr4:103422449..103425804-chr4:103447009..103450716,4	K562	blood:
6	chr4:103421758..103423723-chr4:103430580..103432552,3	MCF-7	breast:
7	chr4:103419957..103425638-chr4:103495824..103504548,11	MCF-7	breast:
8	chr4:103349492..103352803-chr4:103420968..103424398,3	MCF-7	breast:
9	chr4:103438272..103440503-chr4:103440992..103443713,2	MCF-7	breast:
10	chr4:103427425..103429169-chr4:103437672..103439992,2	K562	blood:
11	chr4:103423042..103423659-chr7:72971558..72972250,3	Hela-S3	cervix:
12	chr4:103422194..103424603-chr4:103745115..103749014,4	K562	blood:
13	chr4:103352302..103353294-chr4:103422214..103423235,3	K562	blood:
14	chr4:103422074..103424260-chr4:103435435..103440016,5	K562	blood:
15	chr4:103424918..103427629-chr4:103441760..103444240,2	K562	blood:
16	chr4:103418457..103421752-chr4:103450464..103454174,4	MCF-7	breast:
17	chr4:103442501..103444375-chr4:103444794..103447284,2	K562	blood:
18	chr4:103427680..103429888-chr4:103432571..103434498,2	MCF-7	breast:
19	chr4:103420096..103422829-chr4:103464276..103466057,2	K562	blood:
20	chr11:62606453..62609348-chr4:103421636..103424436,2	MCF-7	breast:
21	chr4:103420745..103423144-chr4:103433405..103436115,3	MCF-7	breast:
22	chr4:103495247..103497005-chr4:103498545..103500219,2	K562	blood:
23	chr3:32022654..32023494-chr4:103422493..103423209,2	Hela-S3	cervix:
24	chr4:103447010..103448533-chr4:103454015..103456334,2	K562	blood:
25	chr4:103489104..103492778-chr4:103495068..103498574,4	MCF-7	breast:
26	chr4:103420331..103423503-chr4:103475320..103478755,3	MCF-7	breast:
27	chr4:103424918..103426820-chr4:103440847..103443260,2	K562	blood:
28	chr4:103442501..103444375-chr4:103444794..103447284,2	K562	blood:
29	chr4:103425524..103427364-chr4:103430743..103433529,2	MCF-7	breast:
30	chr4:103438442..103440658-chr4:103444124..103446101,2	MCF-7	breast:
31	chr4:103440956..103442582-chr4:103451787..103454591,2	MCF-7	breast:
32	chr4:103421642..103424651-chr4:103432017..103435020,7	MCF-7	breast:
33	chr4:103427425..103432192-chr4:103434612..103439992,6	K562	blood:
34	chr20:5986594..5987204-chr4:103422419..103423322,2	HCT-116	colon:
35	chr4:103447755..103449902-chr4:103466038..103467792,2	K562	blood:
36	chr3:49055528..49056300-chr4:103422455..103423039,2	HCT-116	colon:
37	chr4:103481967..103484496-chr4:103488750..103491219,2	MCF-7	breast:
38	chr4:103449757..103452698-chr4:103468709..103470681,2	MCF-7	breast:
39	chr4:103474292..103476069-chr4:103481101..103483068,2	MCF-7	breast:
40	chr4:103434755..103437108-chr4:103437162..103439778,2	MCF-7	breast:
41	chr4:103423143..103423688-chr5:10249942..10250633,2	Hela-S3	cervix:
42	chr4:103438526..103440026-chr4:103449881..103451773,2	K562	blood:
43	chr4:103421335..103424541-chr4:103427509..103429638,4	MCF-7	breast:
44	chr4:103421566..103424767-chr4:103746039..103749014,5	K562	blood:
45	chr4:103421882..103423442-chr4:103462587..103465084,2	MCF-7	breast:
46	chr4:103439093..103441146-chr4:103445747..103447716,2	MCF-7	breast:
47	chr4:103426144..103427805-chr4:103429263..103431794,2	MCF-7	breast:
48	chr4:103462309..103464444-chr4:103468632..103471060,2	MCF-7	breast:
49	chr4:103434755..103437108-chr4:103437162..103439778,2	MCF-7	breast:
50	chr4:103489104..103492778-chr4:103495068..103498574,4	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SLC39A8-1	chr4:103421975-103422476	NONHSAT097590
2	lnc-SLC39A8-1	chr4:103421998-103422476	ENSG00000260651.1

No data

Variant related genes	Relation type
ENSG00000260651	TF binding region
ENSG00000238553	TF binding region
NFKB1	TF binding region
ENSG00000260651	CpG island
ENSG00000238553	CpG island
NFKB1	CpG island
ENSG00000065243	chromatin interactions
ENSG00000246560	chromatin interactions
ENSG00000150756	chromatin interactions
ENSG00000164037	chromatin interactions
ENSG00000251572	chromatin interactions
ENSG00000150753	chromatin interactions
ENSG00000260651	chromatin interactions
ENSG00000088766	chromatin interactions
ENSG00000109332	chromatin interactions
ENSG00000142227	chromatin interactions
ENSG00000234028	chromatin interactions
ENSG00000238553	chromatin interactions
ENSG00000106635	chromatin interactions
ENSG00000144645	chromatin interactions
ENSG00000133316	chromatin interactions
ENSG00000145354	chromatin interactions
ENSG00000178149	chromatin interactions
ENSG00000197385	chromatin interactions
ENSG00000273162	chromatin interactions
ENSG00000109320	chromatin interactions
ENSG00000105479	chromatin interactions
ENSG00000124198	chromatin interactions
ENSG00000138821	chromatin interactions
ENSG00000248161	chromatin interactions

Extended variants
information (count: 2883 )
Associated
traits (count: 78 )

Variant overlapped rSNPs/rCNVs (count:2883 , 50 per page) page: 1 2 3 4 5 6 7 ... 58

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs576049483	chr4:103419380-103419381	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
2	rs186230010	chr4:103419423-103419424	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
3	rs530099218	chr4:103419437-103419438	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
4	rs530185334	chr4:103419522-103419523	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
5	rs567753819	chr4:103419537-103419538	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
6	rs560379843	chr4:103419570-103419571	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
7	rs191938576	chr4:103419572-103419573	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
8	rs184241215	chr4:103419612-103419613	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
9	rs139917233	chr4:103419619-103419620	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
10	rs570973059	chr4:103419631-103419632	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
11	rs531704100	chr4:103419664-103419665	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
12	rs145343814	chr4:103419691-103419692	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
13	rs548303117	chr4:103419732-103419733	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
14	rs535075878	chr4:103419737-103419738	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
15	rs187367324	chr4:103419798-103419799	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
16	rs547731841	chr4:103419855-103419856	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
17	rs565812261	chr4:103419905-103419906	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
18	rs575203503	chr4:103419957-103419958	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs545989429	chr4:103419969-103419970	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs145104176	chr4:103420060-103420061	Weak transcription Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
21	rs557457896	chr4:103420148-103420149	Weak transcription Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
22	rs35054647	chr4:103420162-103420163	Weak transcription Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
23	rs575950515	chr4:103420175-103420176	Weak transcription Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
24	rs561191137	chr4:103420213-103420214	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
25	rs536750049	chr4:103420300-103420301	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
26	rs369705043	chr4:103420319-103420320	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
27	rs555015406	chr4:103420340-103420341	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
28	rs192196344	chr4:103420341-103420342	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
29	rs148679067	chr4:103420377-103420378	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
30	rs560441411	chr4:103420379-103420380	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
31	rs182550101	chr4:103420389-103420390	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
32	rs187252387	chr4:103420402-103420403	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
33	rs142178828	chr4:103420465-103420466	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
34	rs557635287	chr4:103420491-103420492	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
35	rs554928400	chr4:103420519-103420520	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
36	rs368176124	chr4:103420542-103420543	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
37	rs564333131	chr4:103420604-103420605	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
38	rs78023109	chr4:103420609-103420610	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
39	rs550321827	chr4:103420612-103420613	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
40	rs34425291	chr4:103420626-103420627	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
41	rs574643151	chr4:103420672-103420673	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
42	rs562132247	chr4:103420705-103420706	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
43	rs11940017	chr4:103420759-103420760	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
44	rs547607162	chr4:103420762-103420763	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
45	rs566003175	chr4:103420778-103420779	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
46	rs6819775	chr4:103420838-103420839	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
47	rs371002833	chr4:103420843-103420844	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
48	rs569333155	chr4:103420844-103420845	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
49	rs62328539	chr4:103420851-103420852	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
50	rs66641861	chr4:103420852-103420853	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:78)

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
Autism	22495311	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
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	17603634	CNVD
Hepatocellular carcinoma	16750200	CNVD
Myxofibrosarcoma	16751306	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
Adenoid cystic carcinoma	18698036	CNVD
Lung cancer	19208797	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21785460	CNVD
Myelodysplastic syndrome	21251322	CNVD
Lung cancer	18438408	CNVD
Cancer	22429812	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	21183584	CNVD
primary effusion lymphomas	17116491	CNVD
small cell lung cancer	20016488	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17133270	CNVD
T-cell prolymphocytic leukemia	19278963	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
Ovarian cancer	21720365	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Esophageal cancer	21851588	CNVD
Prostate cancer	16573809	CNVD
Multiple myeloma	16616336	CNVD
Melanoma	20688739	CNVD
Breast cancer	16397240	CNVD
Acute myeloid leukemia	18000384	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Myelofibrosis	22110671	CNVD
myeloid cancer	21057493	CNVD
Cancer	20164919	CNVD
Obesity	20935630	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:3167 , 50 per page) page: 1 2 3 4 5 6 7 ... 64

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:103414600-103419400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
2	chr4:103415200-103420400	Weak transcription	Brain Cingulate Gyrus	brain
3	chr4:103415200-103421200	Weak transcription	Brain Substantia Nigra	brain
4	chr4:103415200-103421200	Weak transcription	Left Ventricle	heart
5	chr4:103415200-103421200	Weak transcription	Pancreas	Pancrea
6	chr4:103415200-103421200	Weak transcription	Psoas Muscle	Psoas
7	chr4:103415200-103421400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
8	chr4:103415200-103421400	Weak transcription	Duodenum Mucosa	Duodenum
9	chr4:103415200-103421400	Weak transcription	HMEC	breast
10	chr4:103415400-103421200	Weak transcription	Brain Angular Gyrus	brain
11	chr4:103415400-103421200	Weak transcription	Stomach Mucosa	stomach
12	chr4:103415400-103421400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
13	chr4:103415400-103421400	Weak transcription	Rectal Mucosa Donor 31	rectum
14	chr4:103415400-103421800	Weak transcription	Dnd41	blood
15	chr4:103416000-103421200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
16	chr4:103416000-103421200	Weak transcription	Primary T helper cells PMA-I stimulated	--
17	chr4:103416000-103421200	Weak transcription	Sigmoid Colon	Sigmoid Colon
18	chr4:103416000-103421400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
19	chr4:103416000-103421400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
20	chr4:103417600-103419800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
21	chr4:103417600-103421200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
22	chr4:103418200-103419800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
23	chr4:103418400-103419600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
24	chr4:103418400-103421400	Weak transcription	Fetal Kidney	kidney
25	chr4:103418400-103421400	Weak transcription	Ovary	ovary
26	chr4:103418400-103421400	Weak transcription	K562	blood
27	chr4:103418600-103419400	Enhancers	Fetal Heart	heart
28	chr4:103418600-103420400	Weak transcription	Brain Anterior Caudate	brain
29	chr4:103418600-103420400	Weak transcription	Stomach Smooth Muscle	stomach
30	chr4:103418600-103421200	Weak transcription	Brain Hippocampus Middle	brain
31	chr4:103418800-103420200	Weak transcription	Colon Smooth Muscle	Colon
32	chr4:103418800-103421400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
33	chr4:103419000-103419400	Weak transcription	NHEK	skin
34	chr4:103419200-103419400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
35	chr4:103419400-103419600	Enhancers	NHEK	skin
36	chr4:103419400-103420400	Weak transcription	Fetal Heart	heart
37	chr4:103419400-103421200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
38	chr4:103419600-103419800	Enhancers	Lung	lung
39	chr4:103419600-103421400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
40	chr4:103419600-103421400	Weak transcription	NHEK	skin
41	chr4:103419800-103420600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
42	chr4:103419800-103421400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
43	chr4:103419800-103421600	Weak transcription	Lung	lung
44	chr4:103420000-103420200	Active TSS	Brain Inferior Temporal Lobe	brain
45	chr4:103420200-103420400	Enhancers	Brain Inferior Temporal Lobe	brain
46	chr4:103420200-103421200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
47	chr4:103420200-103421400	Enhancers	Colon Smooth Muscle	Colon
48	chr4:103420400-103420600	Enhancers	Brain Anterior Caudate	brain
49	chr4:103420400-103420600	Enhancers	Brain Cingulate Gyrus	brain
50	chr4:103420400-103420600	Flanking Active TSS	Brain Inferior Temporal Lobe	brain

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