Variant report

Variant	nsv1014936
Chromosome Location	chr2:152019809-152118479
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1210)
CpG islands
(count:916)
Chromatin interactive
region (count:67)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1210 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:152117171-152117929	K562	blood:	n/a	n/a
2	ARID3A	chr2:152095352-152095770	K562	blood:	n/a	n/a
3	ATF2	chr2:152117637-152118442	GM12878	blood:	n/a	n/a
4	BACH1	chr2:152117867-152118629	H1-hESC	embryonic stem cell:	n/a	n/a
5	BCL3	chr2:152094189-152094426	GM12878	blood:	n/a	n/a
6	BCL3	chr2:152118102-152118639	A549	lung:	n/a	chr2:152118125-152118138 chr2:152118112-152118121
7	BCLAF1	chr2:152117664-152118609	GM12878	blood:	n/a	chr2:152118125-152118138 chr2:152118112-152118121
8	BCLAF1	chr2:152117703-152118623	GM12878	blood:	n/a	chr2:152118125-152118138 chr2:152118112-152118121
9	BHLHE40	chr2:152117232-152118903	K562	blood:	n/a	chr2:152118255-152118271
10	BHLHE40	chr2:152117345-152118759	GM12878	blood:	n/a	chr2:152118255-152118271
11	BRCA1	chr2:152117724-152118042	Hela-S3	cervix:	n/a	n/a
12	BRCA1	chr2:152118357-152118478	HepG2	liver:	n/a	n/a
13	BRCA1	chr2:152095212-152095895	H1-hESC	embryonic stem cell:	n/a	n/a
14	CBX3	chr2:152117530-152118987	K562	blood:	n/a	n/a
15	CBX3	chr2:152103967-152104243	K562	blood:	n/a	n/a
16	CBX3	chr2:152105559-152105868	K562	blood:	n/a	n/a
17	CBX3	chr2:152103965-152104263	K562	blood:	n/a	n/a
18	CBX3	chr2:152054005-152054333	K562	blood:	n/a	n/a
19	CBX3	chr2:152117454-152118025	K562	blood:	n/a	n/a
20	CBX3	chr2:152103943-152104371	HCT-116	colon:	n/a	n/a
21	CBX3	chr2:152103953-152104259	HCT-116	colon:	n/a	n/a
22	CCNT2	chr2:152117746-152118742	K562	blood:	n/a	n/a
23	CCNT2	chr2:152054244-152054434	K562	blood:	n/a	n/a
24	CEBPB	chr2:152096177-152096499	A549	lung:	n/a	chr2:152096311-152096322 chr2:152096331-152096342
25	CEBPB	chr2:152095294-152095698	H1-hESC	embryonic stem cell:	n/a	chr2:152095465-152095476
26	CEBPB	chr2:152096147-152096512	Hela-S3	cervix:	n/a	chr2:152096311-152096322 chr2:152096331-152096342
27	CEBPB	chr2:152095250-152095828	A549	lung:	n/a	chr2:152095465-152095476
28	CEBPB	chr2:152065275-152065467	Hela-S3	cervix:	n/a	chr2:152065368-152065379 chr2:152065367-152065380 chr2:152065352-152065365
29	CEBPB	chr2:152053096-152053339	IMR90	lung:	n/a	chr2:152053209-152053220 chr2:152053208-152053221 chr2:152053317-152053328
30	CEBPB	chr2:152095302-152095714	Hela-S3	cervix:	n/a	chr2:152095465-152095476
31	CEBPB	chr2:152117833-152118663	Hela-S3	cervix:	n/a	chr2:152118480-152118491
32	CEBPB	chr2:152095393-152095578	HepG2	liver:	n/a	chr2:152095465-152095476
33	CEBPB	chr2:152118251-152118704	MCF-7	breast:	n/a	chr2:152118480-152118491
34	CEBPB	chr2:152042639-152042984	HepG2	liver:	n/a	n/a
35	CEBPB	chr2:152096212-152096491	IMR90	lung:	n/a	chr2:152096311-152096322 chr2:152096331-152096342
36	CEBPB	chr2:152095074-152095698	A549	lung:	n/a	chr2:152095465-152095476
37	CEBPB	chr2:152096205-152096493	HepG2	liver:	n/a	chr2:152096311-152096322 chr2:152096331-152096342
38	CEBPB	chr2:152068649-152068697	HepG2	liver:	n/a	chr2:152068663-152068674
39	CEBPB	chr2:152087455-152087485	K562	blood:	n/a	n/a
40	CEBPB	chr2:152042718-152042947	A549	lung:	n/a	n/a
41	CEBPB	chr2:152042648-152042868	K562	blood:	n/a	n/a
42	CEBPB	chr2:152095296-152095858	HCT-116	colon:	n/a	chr2:152095465-152095476
43	CEBPB	chr2:152068641-152068706	K562	blood:	n/a	chr2:152068663-152068674
44	CEBPB	chr2:152065337-152065421	HepG2	liver:	n/a	chr2:152065368-152065379 chr2:152065367-152065380 chr2:152065352-152065365
45	CEBPB	chr2:152118316-152118657	K562	blood:	n/a	chr2:152118480-152118491
46	CEBPB	chr2:152095347-152095641	A549	lung:	n/a	chr2:152095465-152095476
47	CEBPB	chr2:152118334-152118666	H1-hESC	embryonic stem cell:	n/a	chr2:152118480-152118491
48	CEBPB	chr2:152095164-152095690	K562	blood:	n/a	chr2:152095465-152095476
49	CEBPB	chr2:152107541-152107941	IMR90	lung:	n/a	n/a
50	CEBPB	chr2:152065293-152065523	IMR90	lung:	n/a	chr2:152065368-152065379 chr2:152065367-152065380 chr2:152065352-152065365

(count:916 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:152118200-152118250	HNPCEpiC	eye:	n/a
2	chr2:152118200-152118250	HNPCEpiC	eye:	n/a
3	chr2:152118435-152118485	HNPCEpiC	eye:	n/a
4	chr2:152042675-152042725	Jurkat	blood:	n/a
5	chr2:152118408-152118458	HEK293	kidney:	embryo
6	chr2:152042657-152042707	IMR90	lung:	fetal
7	chr2:152114699-152114749	HEK293	kidney:	embryo
8	chr2:152092933-152092983	PANC-1	pancreas:	n/a
9	chr2:152042675-152042725	GM12892	blood:	n/a
10	chr2:152042675-152042725	CMK	blood:	n/a
11	chr2:152114699-152114749	SAEC	small airway:	n/a
12	chr2:152118200-152118250	T-47D	breast:	n/a
13	chr2:152106192-152106242	NH-A	brain:	n/a
14	chr2:152118459-152118509	SKMC	muscle:	n/a
15	chr2:152118459-152118509	HepG2	liver:	n/a
16	chr2:152118200-152118250	HAEpiC	amniotic membrane:	n/a
17	chr2:152118010-152118060	ProgFib	skin:	n/a
18	chr2:152118471-152118521	HPAEpiC	pulmonary alveolar:	n/a
19	chr2:152108040-152108090	HRCEpiC	kidney:	n/a
20	chr2:152117022-152117072	PrEC	prostate:	n/a
21	chr2:152118010-152118060	RPTEC	kidney:	n/a
22	chr2:152092933-152092983	SKMC	muscle:	n/a
23	chr2:152118200-152118250	Caco-2	colon:	n/a
24	chr2:152118459-152118509	ovcar-3	ovarian:	n/a
25	chr2:152042675-152042725	HRPEpiC	eye:	n/a
26	chr2:152118010-152118060	AG10803	skin:	n/a
27	chr2:152042657-152042707	ProgFib	skin:	n/a
28	chr2:152042657-152042707	HRCEpiC	kidney:	n/a
29	chr2:152118471-152118521	HUVEC	blood vessel:	n/a
30	chr2:152092933-152092983	GM12878	blood:	n/a
31	chr2:152118010-152118060	SK-N-SH_RA	brain:	n/a
32	chr2:152092933-152092983	T-47D	breast:	n/a
33	chr2:152114699-152114749	AG09319	gingival:	n/a
34	chr2:152118200-152118250	HCT-116	colon:	n/a
35	chr2:152042657-152042707	HNPCEpiC	eye:	n/a
36	chr2:152108040-152108090	HCF	heart:	n/a
37	chr2:152108040-152108090	RPTEC	kidney:	n/a
38	chr2:152118435-152118485	NH-A	brain:	n/a
39	chr2:152118459-152118509	HEK293	kidney:	embryo
40	chr2:152042675-152042725	PrEC	prostate:	n/a
41	chr2:152042657-152042707	GM19239	blood:	n/a
42	chr2:152106192-152106242	PFSK-1	brain:	n/a
43	chr2:152117363-152117413	Hela-S3	cervix:	n/a
44	chr2:152117363-152117413	AG09319	gingival:	n/a
45	chr2:152092933-152092983	IMR90	lung:	fetal
46	chr2:152117363-152117413	SAEC	small airway:	n/a
47	chr2:152118200-152118250	H1-hESC	embryonic stem cell:	embryo
48	chr2:152118408-152118458	MCF-7	breast:	n/a
49	chr2:152092933-152092983	SK-N-SH_RA	brain:	n/a
50	chr2:152118408-152118458	K562	blood:	n/a

(count:67 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr2:152116678..152120470-chr2:152265032..152268454,8	MCF-7	breast:
2	chr2:152020947..152023552-chr2:152026485..152029371,2	K562	blood:
3	chr17:56756857..56758570-chr2:152082974..152084475,2	K562	blood:
4	chr2:152113115..152114989-chr2:152116609..152119218,3	MCF-7	breast:
5	chr2:150451675..150452547-chr2:152095123..152095649,2	MCF-7	breast:
6	chr2:152092689..152095389-chr2:152163780..152166731,2	K562	blood:
7	chr2:152095135..152097024-chr2:152099400..152101186,2	K562	blood:
8	chr17:56735191..56738265-chr2:152082954..152084475,4	MCF-7	breast:
9	chr2:152114220..152115726-chr2:152118400..152119936,2	K562	blood:
10	chr2:152096040..152098295-chr2:152099658..152101934,2	MCF-7	breast:
11	chr2:152101423..152103992-chr2:152110417..152111969,2	K562	blood:
12	chr2:152106609..152109235-chr2:152114382..152116321,2	K562	blood:
13	chr2:152107619..152109429-chr2:152322968..152325434,2	K562	blood:
14	chr17:56735232..56737005-chr2:152082975..152084475,2	MCF-7	breast:
15	chr2:152114819..152117297-chr2:152137988..152139768,2	K562	blood:
16	chr2:152020947..152023552-chr2:152026485..152029371,2	K562	blood:
17	chr2:152117804..152120182-chr2:152144785..152147621,2	MCF-7	breast:
18	chr2:152084091..152085689-chr2:152094268..152097132,2	K562	blood:
19	chr2:152070049..152072600-chr2:152076059..152078560,2	MCF-7	breast:
20	chr2:152075293..152078757-chr2:152080065..152083048,4	MCF-7	breast:
21	chr2:150442857..150445501-chr2:152115437..152118070,2	MCF-7	breast:
22	chr2:152116022..152119511-chr2:152263980..152267786,5	K562	blood:
23	chr2:152002753..152005696-chr2:152094536..152097046,2	K562	blood:
24	chr2:152111081..152114725-chr2:152118123..152119862,3	MCF-7	breast:
25	chr2:152058095..152060460-chr2:152062204..152065058,3	K562	blood:
26	chr2:152116994..152118893-chr2:152266218..152268136,2	MCF-7	breast:
27	chr2:152112196..152114253-chr2:152116352..152117895,2	MCF-7	breast:
28	chr2:152058095..152060460-chr2:152062204..152065058,3	K562	blood:
29	chr2:152036783..152038759-chr2:152047666..152049204,2	K562	blood:
30	chr2:152075293..152078757-chr2:152080065..152083048,4	MCF-7	breast:
31	chr2:152116868..152120610-chr2:152144685..152147660,4	MCF-7	breast:
32	chr2:152117778..152118631-chr7:26240204..26240803,2	NB4	blood:
33	chr2:152117446..152118302-chr8:97247298..97247872,2	HCT-116	colon:
34	chr17:56736211..56737365-chr2:152082954..152083475,4	MCF-7	breast:
35	chr2:152073926..152076724-chr2:152079241..152082233,2	K562	blood:
36	chr2:152015868..152018283-chr2:152021661..152023265,2	MCF-7	breast:
37	chr2:152117973..152120026-chr2:152143620..152147532,3	K562	blood:
38	chr2:152070049..152072600-chr2:152076059..152078560,2	MCF-7	breast:
39	chr2:152101423..152103992-chr2:152110417..152111969,2	K562	blood:
40	chr2:152112196..152114253-chr2:152116352..152117895,2	MCF-7	breast:
41	chr2:151999683..152001762-chr2:152019271..152021804,2	MCF-7	breast:
42	chr2:152105316..152108235-chr2:152116830..152118343,2	K562	blood:
43	chr2:152110867..152113616-chr2:152116296..152118304,2	K562	blood:
44	chr2:152014944..152016964-chr2:152019119..152020652,2	K562	blood:
45	chr2:152036783..152038759-chr2:152047666..152049204,2	K562	blood:
46	chr2:150453759..150454712-chr2:152095488..152096017,2	K562	blood:
47	chr2:152095135..152097024-chr2:152099400..152101186,2	K562	blood:
48	chr2:152033034..152033617-chr2:152201109..152202082,2	MCF-7	breast:
49	chr2:150451575..150452552-chr2:152095332..152096027,4	MCF-7	breast:
50	chr2:152084091..152085689-chr2:152094268..152097132,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RBM43-2	chr2:152102848-152103089	NONHSAT074949
2	lnc-RBM43-1	chr2:152042634-152042723	ENSG00000236885
3	lnc-RBM43-2	chr2:152101986-152102820	NONHSAT074949

No data

Variant related genes	Relation type
FABP5P10	TF binding region
ENSG00000236885	TF binding region
RBM43	TF binding region
FABP5P10	CpG island
ENSG00000236885	CpG island
RBM43	CpG island
ENSG00000122566	chromatin interactions
ENSG00000115963	chromatin interactions
ENSG00000202077	chromatin interactions
ENSG00000200997	chromatin interactions
ENSG00000231969	chromatin interactions
ENSG00000122565	chromatin interactions
ENSG00000168288	chromatin interactions
ENSG00000080345	chromatin interactions
ENSG00000254224	chromatin interactions
ENSG00000156467	chromatin interactions
ENSG00000123609	chromatin interactions
ENSG00000184898	chromatin interactions

Extended variants
information (count: 2715 )
Associated
traits (count: 52 )

Variant overlapped rSNPs/rCNVs (count:2715 , 50 per page) page: 1 2 3 4 5 6 7 ... 55

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs142158470	chr2:152019828-152019829	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs376178385	chr2:152019830-152019831	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs548987792	chr2:152019878-152019879	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs565519791	chr2:152019881-152019882	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs151203417	chr2:152019890-152019891	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs289942	chr2:152019892-152019893	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs289943	chr2:152019935-152019936	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs536850188	chr2:152020007-152020008	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs576011456	chr2:152020035-152020036	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs556694737	chr2:152020052-152020053	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs573809872	chr2:152020089-152020090	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs542726528	chr2:152020092-152020093	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs75119652	chr2:152020111-152020112	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs370447484	chr2:152020139-152020140	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs77965244	chr2:152020141-152020142	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs576763735	chr2:152020177-152020178	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs79304095	chr2:152020197-152020198	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs184684077	chr2:152020216-152020217	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs531189278	chr2:152020226-152020227	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs289944	chr2:152020248-152020249	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs190567127	chr2:152020293-152020294	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs529015565	chr2:152020349-152020350	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs193125065	chr2:152020362-152020363	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs117382582	chr2:152020414-152020415	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs184328624	chr2:152020456-152020457	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs550912812	chr2:152020484-152020485	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs113255637	chr2:152020501-152020502	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs536909367	chr2:152020504-152020505	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs78665211	chr2:152020509-152020510	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs189232193	chr2:152020527-152020528	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs181124426	chr2:152020533-152020534	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs185477466	chr2:152020587-152020588	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs150277028	chr2:152020608-152020609	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs60923351	chr2:152020626-152020627	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs76232110	chr2:152020627-152020628	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs78466832	chr2:152020629-152020630	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs74617686	chr2:152020630-152020631	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs573242520	chr2:152020675-152020676	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs538666428	chr2:152020762-152020763	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs76892433	chr2:152020789-152020790	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs199968921	chr2:152020790-152020791	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs540421398	chr2:152020830-152020831	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs558958243	chr2:152020936-152020937	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs576029867	chr2:152020943-152020944	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs544900947	chr2:152020967-152020968	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs561503441	chr2:152020980-152020981	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs574927038	chr2:152020987-152020988	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs574285571	chr2:152021006-152021007	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs553980007	chr2:152021013-152021014	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs188726764	chr2:152021040-152021041	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:52)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Autism	22495311	CNVD
Autism	18522746	CNVD
Neurodevelopmental disorder	22521361	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Seminomas	18059402	CNVD
Testicular germ cell tumor	18059402	CNVD
Breast cancer	16272173	CNVD
epilepsy	18472482	CNVD
Ewing''s sarcoma	17952124	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Autism	16446308	CNVD
Autism	19401682	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Colorectal cancer	16272173	CNVD
myoclonus epilepsy	18472482	CNVD
Benign familial neonatal-infantile seizures	18472482	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Mental retardation	22214275	CNVD
Glioblastoma	21080181	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	18179710	CNVD
Myelofibrosis	22110671	CNVD
Mental retardation	19156171	CNVD
Acute myeloid leukemia	18000384	CNVD
Autism	20808228	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1002 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:152016200-152021400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
2	chr2:152018000-152020000	Enhancers	Fetal Lung	lung
3	chr2:152018400-152021400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr2:152018600-152021000	Weak transcription	Cortex derived primary cultured neurospheres	brain
5	chr2:152018600-152021600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
6	chr2:152018800-152022200	Weak transcription	HUES64 Cell Line	embryonic stem cell
7	chr2:152019200-152020800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
8	chr2:152019400-152021600	Enhancers	Fetal Brain Male	brain
9	chr2:152019600-152020000	Enhancers	Fetal Muscle Leg	muscle
10	chr2:152019600-152024000	Enhancers	Brain Germinal Matrix	brain
11	chr2:152019800-152020000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr2:152020000-152021000	Weak transcription	Fetal Muscle Leg	muscle
13	chr2:152020400-152021600	Enhancers	Fetal Brain Female	brain
14	chr2:152020800-152022800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
15	chr2:152021000-152021200	Enhancers	Fetal Muscle Leg	muscle
16	chr2:152021000-152022400	Enhancers	Cortex derived primary cultured neurospheres	brain
17	chr2:152021400-152021600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
18	chr2:152021400-152022200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
19	chr2:152021600-152022400	Enhancers	iPS-18 Cell Line	embryonic stem cell
20	chr2:152021600-152022400	Weak transcription	Fetal Brain Female	brain
21	chr2:152022200-152022400	Enhancers	HUES64 Cell Line	embryonic stem cell
22	chr2:152022400-152022600	Enhancers	Fetal Brain Female	brain
23	chr2:152022400-152023200	Weak transcription	HUES64 Cell Line	embryonic stem cell
24	chr2:152022800-152023600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
25	chr2:152023000-152023800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
26	chr2:152023600-152023800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
27	chr2:152023800-152024800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
28	chr2:152024800-152025000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
29	chr2:152029000-152029400	Weak transcription	HUES64 Cell Line	embryonic stem cell
30	chr2:152029400-152029600	Enhancers	HUES64 Cell Line	embryonic stem cell
31	chr2:152029600-152030000	Enhancers	HUES48 Cell Line	embryonic stem cell
32	chr2:152029600-152031200	Weak transcription	HUES64 Cell Line	embryonic stem cell
33	chr2:152030000-152031400	Weak transcription	HUES48 Cell Line	embryonic stem cell
34	chr2:152031200-152033200	Enhancers	H9 Cell Line	embryonic stem cell
35	chr2:152031200-152033600	Enhancers	H1 Cell Line	embryonic stem cell
36	chr2:152031200-152035200	Enhancers	HUES64 Cell Line	embryonic stem cell
37	chr2:152031400-152032000	Enhancers	iPS-18 Cell Line	embryonic stem cell
38	chr2:152031400-152035000	Enhancers	HUES48 Cell Line	embryonic stem cell
39	chr2:152031600-152032600	Enhancers	iPS-15b Cell Line	embryonic stem cell
40	chr2:152031800-152032800	Enhancers	HUES6 Cell Line	embryonic stem cell
41	chr2:152031800-152033000	Enhancers	Fetal Muscle Leg	muscle
42	chr2:152032000-152032600	Enhancers	Brain Germinal Matrix	brain
43	chr2:152032000-152032800	Enhancers	Fetal Muscle Trunk	muscle
44	chr2:152032000-152033600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
45	chr2:152032000-152034400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
46	chr2:152032200-152032600	Enhancers	Breast Myoepithelial Primary Cells	Breast
47	chr2:152032200-152032800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
48	chr2:152032200-152034000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
49	chr2:152032200-152035200	Enhancers	ES-I3 Cell Line	embryonic stem cell
50	chr2:152032600-152032800	Enhancers	iPS-20b Cell Line	embryonic stem cell

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links