Variant report

Variant	nsv556943
Chromosome Location	chr12:1106783-1220688
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:879)
CpG islands
(count:245)
Chromatin interactive
region (count:58)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:879 , 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	chr12:1163435-1164108	HepG2	liver:	n/a	n/a
2	ATF1	chr12:1179144-1179336	K562	blood:	n/a	n/a
3	ATF2	chr12:1189964-1190438	GM12878	blood:	n/a	n/a
4	ATF2	chr12:1107093-1107558	GM12878	blood:	n/a	n/a
5	ATF2	chr12:1208138-1208787	GM12878	blood:	n/a	n/a
6	ATF2	chr12:1107105-1107535	GM12878	blood:	n/a	n/a
7	ATF2	chr12:1208015-1208794	GM12878	blood:	n/a	n/a
8	ATF2	chr12:1189942-1190432	GM12878	blood:	n/a	n/a
9	BACH1	chr12:1192252-1192568	H1-hESC	embryonic stem cell:	n/a	n/a
10	BATF	chr12:1217501-1217717	GM12878	blood:	n/a	n/a
11	BATF	chr12:1208381-1208673	GM12878	blood:	n/a	n/a
12	BATF	chr12:1217437-1217773	GM12878	blood:	n/a	n/a
13	BATF	chr12:1212791-1213131	GM12878	blood:	n/a	chr12:1212980-1212991
14	BATF	chr12:1208306-1208662	GM12878	blood:	n/a	n/a
15	BATF	chr12:1189802-1190073	GM12878	blood:	n/a	n/a
16	BCL11A	chr12:1208360-1208704	GM12878	blood:	n/a	n/a
17	BCL11A	chr12:1189805-1190045	GM12878	blood:	n/a	n/a
18	BCL3	chr12:1150800-1150994	GM12878	blood:	n/a	n/a
19	BCL3	chr12:1208266-1208639	GM12878	blood:	n/a	n/a
20	BCL3	chr12:1150791-1151090	GM12878	blood:	n/a	n/a
21	BCL3	chr12:1189974-1190400	GM12878	blood:	n/a	n/a
22	BCLAF1	chr12:1107112-1107694	GM12878	blood:	n/a	n/a
23	BHLHE40	chr12:1163677-1163970	HepG2	liver:	n/a	n/a
24	BHLHE40	chr12:1107115-1107512	GM12878	blood:	n/a	n/a
25	BHLHE40	chr12:1193133-1193153	GM12878	blood:	n/a	n/a
26	BRCA1	chr12:1189702-1189919	GM12878	blood:	n/a	n/a
27	CEBPB	chr12:1107668-1107969	HepG2	liver:	n/a	chr12:1107835-1107846
28	CEBPB	chr12:1219018-1219304	A549	lung:	n/a	chr12:1219163-1219174
29	CEBPB	chr12:1175887-1176058	IMR90	lung:	n/a	n/a
30	CEBPB	chr12:1107713-1107927	HepG2	liver:	n/a	chr12:1107835-1107846
31	CEBPB	chr12:1163627-1163960	HepG2	liver:	n/a	n/a
32	CEBPB	chr12:1107735-1107884	K562	blood:	n/a	chr12:1107835-1107846
33	CEBPB	chr12:1219099-1219334	MCF-7	breast:	n/a	chr12:1219163-1219174
34	CEBPB	chr12:1107643-1108030	HepG2	liver:	n/a	chr12:1107835-1107846
35	CEBPB	chr12:1131460-1131797	IMR90	lung:	n/a	chr12:1131628-1131639
36	CEBPB	chr12:1107660-1108031	HepG2	liver:	n/a	chr12:1107835-1107846
37	CEBPB	chr12:1216224-1216256	H1-hESC	embryonic stem cell:	n/a	n/a
38	CEBPB	chr12:1175921-1176099	A549	lung:	n/a	n/a
39	CEBPB	chr12:1202010-1202206	H1-hESC	embryonic stem cell:	n/a	chr12:1202077-1202088
40	CEBPB	chr12:1107666-1107985	K562	blood:	n/a	chr12:1107835-1107846
41	CEBPB	chr12:1219064-1219233	Hela-S3	cervix:	n/a	chr12:1219163-1219174
42	CEBPB	chr12:1201980-1202204	MCF-7	breast:	n/a	chr12:1202077-1202088
43	CEBPB	chr12:1175918-1176030	K562	blood:	n/a	n/a
44	CEBPB	chr12:1201989-1202128	IMR90	lung:	n/a	chr12:1202077-1202088
45	CEBPB	chr12:1216107-1216352	K562	blood:	n/a	chr12:1216222-1216235
46	CEBPB	chr12:1163620-1163996	HepG2	liver:	n/a	n/a
47	CEBPB	chr12:1140023-1140300	HepG2	liver:	n/a	chr12:1140123-1140134 chr12:1140159-1140170
48	CEBPB	chr12:1138801-1139142	IMR90	lung:	n/a	chr12:1138969-1138980
49	CEBPB	chr12:1123306-1123669	Hela-S3	cervix:	n/a	n/a
50	CEBPB	chr12:1219018-1219252	IMR90	lung:	n/a	chr12:1219163-1219174

(count:245 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:1210875-1210925	AG04450	lung:	fetal
2	chr12:1210875-1210925	AG04450	lung:	fetal
3	chr12:1137376-1137426	H1-hESC	embryonic stem cell:	embryo
4	chr12:1137376-1137426	HRE	kidney:	n/a
5	chr12:1192425-1192475	ProgFib	skin:	n/a
6	chr12:1192425-1192475	Hela-S3	cervix:	n/a
7	chr12:1137376-1137426	AG04449	skin:	fetal
8	chr12:1210875-1210925	SAEC	small airway:	n/a
9	chr12:1137376-1137426	Jurkat	blood:	n/a
10	chr12:1137376-1137426	Hepatocyte	liver:	n/a
11	chr12:1157718-1157768	AG04449	skin:	fetal
12	chr12:1192425-1192475	CMK	blood:	n/a
13	chr12:1157718-1157768	NHBE	bronchial:	n/a
14	chr12:1192425-1192475	PrEC	prostate:	n/a
15	chr12:1210875-1210925	Hela-S3	cervix:	n/a
16	chr12:1192425-1192475	HCPEpiC	choroid plexus:	n/a
17	chr12:1137376-1137426	MCF10A-Er-Src	breast:	n/a
18	chr12:1210875-1210925	SK-N-SH_RA	brain:	n/a
19	chr12:1192425-1192475	K562	blood:	n/a
20	chr12:1192425-1192475	HCT-116	colon:	n/a
21	chr12:1210875-1210925	PrEC	prostate:	n/a
22	chr12:1137376-1137426	SAEC	small airway:	n/a
23	chr12:1192425-1192475	SAEC	small airway:	n/a
24	chr12:1210875-1210925	AG04449	skin:	fetal
25	chr12:1210875-1210925	Hepatocyte	liver:	n/a
26	chr12:1157718-1157768	IMR90	lung:	fetal
27	chr12:1210875-1210925	HCM	heart:	n/a
28	chr12:1192425-1192475	AG09319	gingival:	n/a
29	chr12:1157718-1157768	HCF	heart:	n/a
30	chr12:1210875-1210925	NH-A	brain:	n/a
31	chr12:1192425-1192475	U87	brain:	n/a
32	chr12:1157718-1157768	HMEC	breast:	n/a
33	chr12:1137376-1137426	HIPEpiC	eye:	n/a
34	chr12:1157718-1157768	SK-N-SH	brain:	n/a
35	chr12:1157718-1157768	SK-N-SH_RA	brain:	n/a
36	chr12:1192425-1192475	AoSMC	blood vessel:	n/a
37	chr12:1192425-1192475	SK-N-SH_RA	brain:	n/a
38	chr12:1210875-1210925	ProgFib	skin:	n/a
39	chr12:1210875-1210925	HepG2	liver:	n/a
40	chr12:1157718-1157768	PFSK-1	brain:	n/a
41	chr12:1192425-1192475	SK-N-MC	brain:	n/a
42	chr12:1192425-1192475	HEK293	kidney:	embryo
43	chr12:1137376-1137426	LNCaP	prostate:	n/a
44	chr12:1192425-1192475	HUVEC	blood vessel:	n/a
45	chr12:1157718-1157768	HRPEpiC	eye:	n/a
46	chr12:1137376-1137426	HPAEpiC	pulmonary alveolar:	n/a
47	chr12:1137376-1137426	GM12878	blood:	n/a
48	chr12:1157718-1157768	T-47D	breast:	n/a
49	chr12:1210875-1210925	PANC-1	pancreas:	n/a
50	chr12:1210875-1210925	LNCaP	prostate:	n/a

(count:58 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr12:1152891..1155598-chr12:1157921..1160119,2	MCF-7	breast:
2	chr12:1207282..1210142-chr12:1212325..1214005,2	MCF-7	breast:
3	chr12:1106615..1109264-chr12:1111122..1112968,2	K562	blood:
4	chr12:1105575..1107206-chr12:1112687..1115441,2	MCF-7	breast:
5	chr12:1191732..1194399-chr12:1201546..1203517,2	K562	blood:
6	chr12:1099395..1101997-chr12:1116797..1119269,2	MCF-7	breast:
7	chr12:1213022..1214727-chr12:1218938..1221274,2	K562	blood:
8	chr12:1115484..1118405-chr12:1144676..1146516,2	K562	blood:
9	chr12:1099164..1100750-chr12:1199458..1202097,2	MCF-7	breast:
10	chr12:1161679..1164344-chr12:1168247..1169852,2	MCF-7	breast:
11	chr12:1157626..1159829-chr12:1163516..1166184,2	K562	blood:
12	chr12:1123645..1125467-chr12:1128602..1130622,2	MCF-7	breast:
13	chr12:1058398..1059945-chr12:1134448..1137215,2	MCF-7	breast:
14	chr12:1152891..1155598-chr12:1157921..1160119,2	MCF-7	breast:
15	chr12:1112403..1114788-chr12:1124041..1126643,2	MCF-7	breast:
16	chr12:1219719..1221721-chr12:1225249..1227124,3	K562	blood:
17	chr12:1213022..1214727-chr12:1218938..1221274,2	K562	blood:
18	chr12:1098745..1101641-chr12:1113139..1115452,2	MCF-7	breast:
19	chr12:1152382..1155003-chr12:1155624..1158395,2	MCF-7	breast:
20	chr12:1105236..1108232-chr12:1119325..1121550,2	K562	blood:
21	chr12:1123645..1125467-chr12:1128602..1130622,2	MCF-7	breast:
22	chr12:1124432..1126227-chr12:1128822..1131462,2	K562	blood:
23	chr12:1098483..1100095-chr12:1136049..1138258,2	K562	blood:
24	chr12:1218934..1220880-chr12:1702638..1704337,2	MCF-7	breast:
25	chr12:1124727..1126388-chr12:1127610..1130322,2	K562	blood:
26	chr12:1207282..1210142-chr12:1212325..1214005,2	MCF-7	breast:
27	chr12:1124432..1126227-chr12:1128822..1131462,2	K562	blood:
28	chr12:1115484..1118405-chr12:1144676..1146516,2	K562	blood:
29	chr12:1124727..1126388-chr12:1127610..1130322,2	K562	blood:
30	chr12:1106383..1108991-chr12:1173040..1176603,3	MCF-7	breast:
31	chr12:1121748..1124121-chr12:1125522..1128122,2	K562	blood:
32	chr12:1098834..1102191-chr12:1145986..1148768,3	MCF-7	breast:
33	chr12:1097166..1102781-chr12:1103327..1109862,10	MCF-7	breast:
34	chr12:1112403..1114788-chr12:1124041..1126643,2	MCF-7	breast:
35	chr12:1175408..1176101-chr12:1202225..1202957,2	MCF-7	breast:
36	chr12:1105236..1108232-chr12:1119325..1121550,2	K562	blood:
37	chr12:1100051..1101889-chr12:1154159..1157012,2	MCF-7	breast:
38	chr12:1057331..1059748-chr12:1192287..1193829,2	MCF-7	breast:
39	chr12:1144079..1146307-chr12:1153317..1156042,2	MCF-7	breast:
40	chr12:1157626..1159829-chr12:1163516..1166184,2	K562	blood:
41	chr12:1099457..1102030-chr12:1124374..1127197,2	MCF-7	breast:
42	chr12:1099506..1101542-chr12:1147987..1150794,2	MCF-7	breast:
43	chr12:1102489..1104981-chr12:1121749..1123712,2	MCF-7	breast:
44	chr12:1161679..1164344-chr12:1168247..1169852,2	MCF-7	breast:
45	chr12:1144079..1146307-chr12:1153317..1156042,2	MCF-7	breast:
46	chr10:34303831..34306483-chr12:1141784..1144309,2	MCF-7	breast:
47	chr12:1099208..1102157-chr12:1111838..1114594,2	K562	blood:
48	chr12:1215657..1217176-chr12:1696777..1699113,2	MCF-7	breast:
49	chr12:1105575..1107206-chr12:1112687..1115441,2	MCF-7	breast:
50	chr12:1099800..1103499-chr12:1103569..1107416,6	MCF-7	breast:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-WNK1-3	chr12:1107488-1107648	NONHSAT025382
2	lnc-WNK1-3	chr12:1136914-1137008	NONHSAT025382
3	lnc-RAD52-1	chr12:1162266-1162823	predAs_chen_BG198287_1
4	lnc-WNK1-2	chr12:1119501-1119792	NONHSAT025383

No data

Variant related genes	Relation type
ERC1	TF binding region
RN7SL852P	TF binding region
ERC1	CpG island
RN7SL852P	CpG island
ENSG00000171823	chromatin interactions
ENSG00000265997	chromatin interactions
ENSG00000082805	chromatin interactions
ENSG00000002016	chromatin interactions
ENSG00000250132	chromatin interactions

Extended variants
information (count: 4296 )
Associated
traits (count: 86 )

Variant overlapped rSNPs/rCNVs (count:4296 , 50 per page) page: 1 2 3 4 5 6 7 ... 86

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7954858	chr12:1106783-1106784	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs567280203	chr12:1106793-1106794	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
3	rs537882063	chr12:1106838-1106839	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
4	rs145354152	chr12:1106878-1106879	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
5	rs577702159	chr12:1106879-1106880	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
6	rs557972101	chr12:1106908-1106909	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
7	rs574070226	chr12:1106914-1106915	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
8	rs147242775	chr12:1106954-1106955	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
9	rs187979846	chr12:1106963-1106964	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
10	rs373390174	chr12:1107060-1107061	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
11	rs181878273	chr12:1107120-1107121	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
12	rs562082310	chr12:1107244-1107245	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
13	rs529537116	chr12:1107300-1107301	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
14	rs544225098	chr12:1107315-1107316	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
15	rs79756180	chr12:1107324-1107325	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
16	rs58568292	chr12:1107334-1107335	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs186134610	chr12:1107376-1107377	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
18	rs190387612	chr12:1107399-1107400	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
19	rs139663940	chr12:1107421-1107422	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
20	rs549191064	chr12:1107443-1107444	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
21	rs567611326	chr12:1107444-1107445	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
22	rs374517935	chr12:1107448-1107449	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
23	rs538116662	chr12:1107461-1107462	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
24	rs149739621	chr12:1107525-1107526	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
25	rs73606369	chr12:1107527-1107528	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region lncRNA	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs375721723	chr12:1107541-1107542	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
27	rs181658257	chr12:1107571-1107572	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
28	rs541549724	chr12:1107603-1107604	Weak transcription Enhancers Strong transcription Genic enhancers Active TSS Flanking Active TSS	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
29	rs370008554	chr12:1107613-1107614	Weak transcription Enhancers Strong transcription Genic enhancers Active TSS Flanking Active TSS	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
30	rs540911843	chr12:1107636-1107637	Weak transcription Enhancers Strong transcription Genic enhancers Active TSS Flanking Active TSS	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
31	rs570132541	chr12:1107728-1107729	Weak transcription Enhancers Strong transcription Genic enhancers Active TSS Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
32	rs374070587	chr12:1107733-1107734	Weak transcription Enhancers Strong transcription Genic enhancers Active TSS Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
33	rs534167121	chr12:1107772-1107773	Weak transcription Enhancers Strong transcription Genic enhancers Active TSS Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
34	rs555516279	chr12:1107802-1107803	Weak transcription Enhancers Strong transcription Genic enhancers Active TSS Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
35	rs11064633	chr12:1107830-1107831	Weak transcription Enhancers Strong transcription Genic enhancers Active TSS Flanking Active TSS	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
36	rs544471653	chr12:1107896-1107897	Weak transcription Enhancers Strong transcription Genic enhancers Active TSS Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
37	rs58485343	chr12:1107929-1107930	Weak transcription Enhancers Strong transcription Genic enhancers Active TSS Flanking Active TSS	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs148882699	chr12:1107957-1107958	Weak transcription Enhancers Strong transcription Genic enhancers Active TSS Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
39	rs545495291	chr12:1108010-1108011	Weak transcription Strong transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
40	rs56884625	chr12:1108017-1108018	Weak transcription Strong transcription Enhancers	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs527367596	chr12:1108020-1108021	Weak transcription Strong transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
42	rs527784104	chr12:1108079-1108080	Weak transcription Strong transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
43	rs549227953	chr12:1108081-1108082	Weak transcription Strong transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
44	rs561029928	chr12:1108087-1108088	Weak transcription Strong transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
45	rs531661099	chr12:1108148-1108149	Weak transcription Strong transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
46	rs549762191	chr12:1108218-1108219	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
47	rs144072535	chr12:1108270-1108271	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs11064634	chr12:1108304-1108305	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs186763317	chr12:1108315-1108316	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs544944474	chr12:1108384-1108385	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:86)

Disease	PMID	Source
Cancer	20164920	CNVD
Myelofibrosis	22110671	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Glaucoma	21310917	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Malignant peripheral nerve sheath tumor	19844265	CNVD
Squamous cell cancer	19607727	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Hepatocellular carcinoma	16750200	CNVD
Breast cancer	17133270	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Mental retardation	17847001	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
abnormal development	18461090	CNVD
Ovarian cancer	20844748	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Medulloblastoma	16968546	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Breast cancer	22032731	CNVD
Cancer	21183584	CNVD
Myxofibrosarcoma	16751306	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Prostate cancer	21965145	CNVD
Acute myeloid leukemia	16864856	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Disorders of sex development	21048976	CNVD
Glioblastoma multiforme	21080181	CNVD
Liposarcoma	21253554	CNVD
Prostate cancer	19156837	CNVD
Emphysema	19352772	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Malignant germ cell tumour	17285132	CNVD
Melanoma	18172304	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Wilms tumour	21544195	CNVD
Squamous cell cancer	21044232	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	19960244	CNVD
Endometrial cancer	22040021	CNVD
Colorectal cancer	20709793	CNVD
Breast cancer	21264507	CNVD
Cancer	16751803	CNVD
Testicular cancer	18059402	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Seminomas	18059402	CNVD
Esophageal cancer	21851588	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Testicular germ cell tumor	18059402	CNVD
Malaria	21533027	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Ewing''s sarcoma	17952124	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21858162	CNVD
Breast cancer	21509527	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21785460	CNVD
Ovarian cancer	21720365	CNVD
Myelodysplastic syndrome	21251322	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Cancer	17440070	CNVD
Autism	22495311	CNVD
Pancreatic cancer	17952125	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1963 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:1101000-1123000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr12:1101200-1112800	Weak transcription	Gastric	stomach
3	chr12:1101200-1112800	Weak transcription	Ovary	ovary
4	chr12:1101200-1137000	Weak transcription	Lung	lung
5	chr12:1101400-1113000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr12:1101400-1115400	Weak transcription	Esophagus	oesophagus
7	chr12:1101600-1107400	Weak transcription	HSMM	muscle
8	chr12:1101600-1109800	Weak transcription	Fetal Stomach	stomach
9	chr12:1101600-1112600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr12:1101600-1112800	Weak transcription	Primary T cells fromperipheralblood	blood
11	chr12:1101600-1112800	Weak transcription	Fetal Thymus	thymus
12	chr12:1101600-1112800	Weak transcription	Right Ventricle	heart
13	chr12:1101600-1112800	Weak transcription	Thymus	Thymus
14	chr12:1101600-1113200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
15	chr12:1101600-1116200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
16	chr12:1101600-1116200	Weak transcription	Small Intestine	intestine
17	chr12:1101600-1130400	Weak transcription	Fetal Muscle Trunk	muscle
18	chr12:1101600-1136800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
19	chr12:1101600-1136800	Weak transcription	Fetal Muscle Leg	muscle
20	chr12:1101600-1137000	Weak transcription	Rectal Mucosa Donor 31	rectum
21	chr12:1101800-1112800	Weak transcription	Right Atrium	heart
22	chr12:1101800-1131000	Weak transcription	Primary B cells from cord blood	blood
23	chr12:1102000-1107400	Weak transcription	Duodenum Mucosa	Duodenum
24	chr12:1102000-1110400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
25	chr12:1102000-1110400	Weak transcription	Stomach Smooth Muscle	stomach
26	chr12:1102000-1112600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
27	chr12:1102000-1112800	Weak transcription	Brain Germinal Matrix	brain
28	chr12:1102000-1112800	Weak transcription	Fetal Intestine Small	intestine
29	chr12:1102000-1122800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
30	chr12:1102000-1137000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
31	chr12:1102000-1137200	Weak transcription	Fetal Lung	lung
32	chr12:1102200-1107600	Weak transcription	Fetal Intestine Large	intestine
33	chr12:1102200-1110400	Weak transcription	HUES48 Cell Line	embryonic stem cell
34	chr12:1102200-1112400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
35	chr12:1102200-1112600	Weak transcription	HUES6 Cell Line	embryonic stem cell
36	chr12:1102200-1112600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
37	chr12:1102200-1112800	Weak transcription	Brain Hippocampus Middle	brain
38	chr12:1102200-1118800	Weak transcription	Fetal Brain Male	brain
39	chr12:1102200-1122600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
40	chr12:1102200-1129000	Weak transcription	Primary T cells from cord blood	blood
41	chr12:1102200-1131000	Weak transcription	Primary hematopoietic stem cells	blood
42	chr12:1102200-1131400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
43	chr12:1102200-1135200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
44	chr12:1102400-1112400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
45	chr12:1102400-1112600	Weak transcription	Cortex derived primary cultured neurospheres	brain
46	chr12:1102400-1112800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
47	chr12:1102600-1106800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
48	chr12:1102600-1106800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
49	chr12:1102600-1107000	Weak transcription	Pancreatic Islets	Pancreatic Islet
50	chr12:1102600-1110200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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