Variant report

Variant	nsv533782
Chromosome Location	chr2:183059730-183500040
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1936)
CpG islands
(count:1892)
Chromatin interactive
region (count:67)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1936 , 50 per page) page: 1 2 3 4 5 6 7 ... 39

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:183105472-183105968	HepG2	liver:	n/a	n/a
2	ARID3A	chr2:183481518-183482276	HepG2	liver:	n/a	n/a
3	ARID3A	chr2:183460601-183460670	K562	blood:	n/a	n/a
4	ARID3A	chr2:183483411-183483533	K562	blood:	n/a	n/a
5	ATF2	chr2:183110648-183110961	GM12878	blood:	n/a	n/a
6	BACH1	chr2:183128564-183128593	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr2:183490541-183490891	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr2:183413092-183413127	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr2:183107362-183107550	H1-hESC	embryonic stem cell:	n/a	n/a
10	BATF	chr2:183105570-183105896	GM12878	blood:	n/a	n/a
11	BATF	chr2:183110684-183111025	GM12878	blood:	n/a	n/a
12	BATF	chr2:183105612-183105996	GM12878	blood:	n/a	n/a
13	BATF	chr2:183471691-183471996	GM12878	blood:	n/a	chr2:183471798-183471809
14	BATF	chr2:183460356-183460628	GM12878	blood:	n/a	n/a
15	BATF	chr2:183110630-183111009	GM12878	blood:	n/a	n/a
16	BCL11A	chr2:183105671-183105923	GM12878	blood:	n/a	chr2:183105754-183105763
17	BCL11A	chr2:183110662-183110954	GM12878	blood:	n/a	n/a
18	BCL11A	chr2:183471755-183471955	GM12878	blood:	n/a	n/a
19	BCL11A	chr2:183471694-183472024	GM12878	blood:	n/a	n/a
20	BCL11A	chr2:183110738-183110944	GM12878	blood:	n/a	n/a
21	BCL11A	chr2:183105580-183105957	GM12878	blood:	n/a	chr2:183105754-183105763
22	BCL3	chr2:183231250-183231948	A549	lung:	n/a	n/a
23	BCL3	chr2:183216612-183216884	GM12878	blood:	n/a	n/a
24	BCL3	chr2:183216207-183216552	GM12878	blood:	n/a	n/a
25	BCLAF1	chr2:183105461-183106039	GM12878	blood:	n/a	chr2:183105754-183105763
26	BHLHE40	chr2:183483428-183483594	K562	blood:	n/a	n/a
27	BHLHE40	chr2:183481919-183482224	HepG2	liver:	n/a	n/a
28	BHLHE40	chr2:183475883-183475985	K562	blood:	n/a	n/a
29	BHLHE40	chr2:183090280-183090425	GM12878	blood:	n/a	n/a
30	BRCA1	chr2:183231396-183231828	Hela-S3	cervix:	n/a	n/a
31	BRCA1	chr2:183165364-183166161	Hela-S3	cervix:	n/a	n/a
32	CBX3	chr2:183237165-183238178	HCT-116	colon:	n/a	n/a
33	CBX3	chr2:183249509-183249933	HCT-116	colon:	n/a	n/a
34	CBX3	chr2:183237279-183237999	HCT-116	colon:	n/a	n/a
35	CCNT2	chr2:183483419-183483635	K562	blood:	n/a	n/a
36	CCNT2	chr2:183410365-183410490	K562	blood:	n/a	n/a
37	CEBPB	chr2:183470879-183471036	Hela-S3	cervix:	n/a	n/a
38	CEBPB	chr2:183462303-183462651	K562	blood:	n/a	n/a
39	CEBPB	chr2:183310193-183310620	Hela-S3	cervix:	n/a	chr2:183310406-183310418
40	CEBPB	chr2:183183738-183183975	K562	blood:	n/a	chr2:183183846-183183857 chr2:183183847-183183856 chr2:183183845-183183858 chr2:183183845-183183858 chr2:183183847-183183856 chr2:183183847-183183856 chr2:183183845-183183858 chr2:183183845-183183856 chr2:183183845-183183856 chr2:183183847-183183856
41	CEBPB	chr2:183189358-183189746	ECC-1	luminal epithelium:	n/a	n/a
42	CEBPB	chr2:183462351-183462551	Hela-S3	cervix:	n/a	n/a
43	CEBPB	chr2:183105637-183106115	HepG2	liver:	n/a	n/a
44	CEBPB	chr2:183368280-183368966	IMR90	lung:	n/a	n/a
45	CEBPB	chr2:183231373-183231769	IMR90	lung:	n/a	n/a
46	CEBPB	chr2:183369596-183369995	IMR90	lung:	n/a	n/a
47	CEBPB	chr2:183290856-183291196	HepG2	liver:	n/a	chr2:183291025-183291038 chr2:183291025-183291038 chr2:183291025-183291036
48	CEBPB	chr2:183223154-183223442	A549	lung:	n/a	chr2:183223293-183223304
49	CEBPB	chr2:183452619-183452982	IMR90	lung:	n/a	n/a
50	CEBPB	chr2:183151192-183151252	HepG2	liver:	n/a	n/a

(count:1892 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:183498282-183498332	HUVEC	blood vessel:	n/a
2	chr2:183498282-183498332	HUVEC	blood vessel:	n/a
3	chr2:183292922-183292972	AG09319	gingival:	n/a
4	chr2:183107046-183107096	HCT-116	colon:	n/a
5	chr2:183387015-183387065	K562	blood:	n/a
6	chr2:183370084-183370134	HMEC	breast:	n/a
7	chr2:183292092-183292142	ProgFib	skin:	n/a
8	chr2:183123847-183123897	A549	lung:	n/a
9	chr2:183370084-183370134	HUVEC	blood vessel:	n/a
10	chr2:183107220-183107270	AG09309	skin:	n/a
11	chr2:183086277-183086327	GM12892	blood:	n/a
12	chr2:183237787-183237837	HCM	heart:	n/a
13	chr2:183321813-183321863	AG10803	skin:	n/a
14	chr2:183244218-183244268	Caco-2	colon:	n/a
15	chr2:183473236-183473286	PFSK-1	brain:	n/a
16	chr2:183183274-183183324	NT2-D1	testis:	n/a
17	chr2:183107220-183107270	HRE	kidney:	n/a
18	chr2:183387015-183387065	AG09319	gingival:	n/a
19	chr2:183123847-183123897	HEK293	kidney:	embryo
20	chr2:183489804-183489854	HL-60	blood:	n/a
21	chr2:183123847-183123897	AG04449	skin:	fetal
22	chr2:183489804-183489854	GM19239	blood:	n/a
23	chr2:183106125-183106175	HRE	kidney:	n/a
24	chr2:183387885-183387935	U87	brain:	n/a
25	chr2:183489804-183489854	Hela-S3	cervix:	n/a
26	chr2:183387885-183387935	HUVEC	blood vessel:	n/a
27	chr2:183457634-183457684	K562	blood:	n/a
28	chr2:183473411-183473461	HRCEpiC	kidney:	n/a
29	chr2:183387501-183387551	AoSMC	blood vessel:	n/a
30	chr2:183291758-183291808	HIPEpiC	eye:	n/a
31	chr2:183473236-183473286	NT2-D1	testis:	n/a
32	chr2:183277810-183277860	HMEC	breast:	n/a
33	chr2:183237787-183237837	HAEpiC	amniotic membrane:	n/a
34	chr2:183458286-183458336	AG09309	skin:	n/a
35	chr2:183321813-183321863	HEK293	kidney:	embryo
36	chr2:183387015-183387065	RPTEC	kidney:	n/a
37	chr2:183457634-183457684	NT2-D1	testis:	n/a
38	chr2:183291758-183291808	U87	brain:	n/a
39	chr2:183473236-183473286	IMR90	lung:	fetal
40	chr2:183321813-183321863	AG09309	skin:	n/a
41	chr2:183489804-183489854	SKMC	muscle:	n/a
42	chr2:183473411-183473461	HepG2	liver:	n/a
43	chr2:183107220-183107270	HL-60	blood:	n/a
44	chr2:183498282-183498332	HCPEpiC	choroid plexus:	n/a
45	chr2:183498282-183498332	LNCaP	prostate:	n/a
46	chr2:183277810-183277860	SAEC	small airway:	n/a
47	chr2:183473411-183473461	SK-N-SH	brain:	n/a
48	chr2:183321813-183321863	HEEpiC	esophagus:	n/a
49	chr2:183292092-183292142	HepG2	liver:	n/a
50	chr2:183107220-183107270	NB4	blood:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr2:183485234..183486908-chr2:183488749..183490647,2	K562	blood:
2	chr2:183165658..183166473-chr2:183513729..183514661,3	MCF-7	breast:
3	chr2:183297531..183299912-chr2:183299956..183302678,2	K562	blood:
4	chr2:183415450..183417641-chr2:183419320..183421411,2	K562	blood:
5	chr2:183407157..183409269-chr2:183412477..183414356,2	K562	blood:
6	chr2:183220786..183225092-chr2:183225248..183228403,3	MCF-7	breast:
7	chr2:183462276..183465034-chr2:183470042..183471619,2	K562	blood:
8	chr2:183220786..183225092-chr2:183225248..183228403,3	MCF-7	breast:
9	chr2:183105303..183105848-chr2:183450937..183451448,2	MCF-7	breast:
10	chr2:183381297..183382810-chr2:183385812..183388467,2	K562	blood:
11	chr2:183172864..183175852-chr2:183181543..183183109,2	K562	blood:
12	chr2:183398225..183399816-chr2:183400215..183403060,2	MCF-7	breast:
13	chr2:183484463..183486734-chr2:183489147..183491693,3	K562	blood:
14	chr2:183182727..183184381-chr2:183186031..183187729,2	K562	blood:
15	chr2:183398225..183399816-chr2:183400215..183403060,2	MCF-7	breast:
16	chr2:183410632..183412807-chr2:183450091..183453006,2	K562	blood:
17	chr2:183492322..183494288-chr2:183495772..183497912,2	K562	blood:
18	chr2:183285134..183287339-chr2:183293289..183296061,2	K562	blood:
19	chr2:183296401..183298106-chr2:183311342..183313093,2	K562	blood:
20	chr2:183139290..183141946-chr2:183155474..183158091,2	K562	blood:
21	chr2:183335532..183337618-chr2:183340373..183342974,2	K562	blood:
22	chr2:183410632..183412807-chr2:183450091..183453006,2	K562	blood:
23	chr2:183485446..183488008-chr2:183493899..183496895,2	K562	blood:
24	chr12:82936658..82939200-chr2:183214684..183217154,2	MCF-7	breast:
25	chr2:183325057..183326924-chr2:183328449..183330084,2	K562	blood:
26	chr2:183492322..183494288-chr2:183495772..183497912,2	K562	blood:
27	chr2:183279201..183281730-chr2:183282038..183284679,2	MCF-7	breast:
28	chr2:183279805..183282576-chr2:183283431..183285947,2	MCF-7	breast:
29	chr2:183182727..183184381-chr2:183186031..183187729,2	K562	blood:
30	chr2:183472950..183474900-chr2:183475047..183476914,2	K562	blood:
31	chr2:183172864..183175852-chr2:183181543..183183109,2	K562	blood:
32	chr2:183179551..183180178-chr3:111918314..111918885,2	MCF-7	breast:
33	chr2:183296401..183298106-chr2:183311342..183313093,2	K562	blood:
34	chr2:183344989..183346517-chr2:183352874..183355064,2	MCF-7	breast:
35	chr2:183485446..183488008-chr2:183493899..183496895,2	K562	blood:
36	chr2:183103040..183104711-chr2:183106820..183108898,2	K562	blood:
37	chr2:183409611..183411975-chr2:183412414..183414560,2	K562	blood:
38	chr2:183223904..183227236-chr2:183228797..183232195,3	K562	blood:
39	chr2:183139290..183141946-chr2:183155474..183158091,2	K562	blood:
40	chr2:183223904..183227236-chr2:183228797..183232195,3	K562	blood:
41	chr2:183485234..183486908-chr2:183488749..183490647,2	K562	blood:
42	chr2:183484463..183486734-chr2:183489147..183491693,3	K562	blood:
43	chr2:183285134..183287339-chr2:183293289..183296061,2	K562	blood:
44	chr2:183325057..183326924-chr2:183328449..183330084,2	K562	blood:
45	chr2:183406601..183409032-chr2:183409704..183411675,2	K562	blood:
46	chr2:183165936..183166478-chr2:183451147..183451888,2	MCF-7	breast:
47	chr2:183105303..183105848-chr2:183450937..183451448,2	MCF-7	breast:
48	chr2:183261575..183263356-chr2:183271922..183273654,2	K562	blood:
49	chr2:183297531..183299912-chr2:183299956..183302678,2	K562	blood:
50	chr2:183291063..183292586-chr2:183298159..183300836,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PPP1R1C-3	chr2:183179011-183179269	NONHSAT075907

No data

Variant related genes	Relation type
RN7SL267P	TF binding region
PDE1A	TF binding region
RN7SL267P	CpG island
PDE1A	CpG island
ENSG00000115252	chromatin interactions

Extended variants
information (count: 15214 )
Associated
traits (count: 62 )

Variant overlapped rSNPs/rCNVs (count:15214 , 50 per page) page: 1 2 3 4 5 6 7 ... 305

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs564765676	chr2:183059745-183059746	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs180921856	chr2:183059809-183059810	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs145924931	chr2:183059819-183059820	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs542450213	chr2:183059843-183059844	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs534830435	chr2:183059865-183059866	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs139812301	chr2:183059882-183059883	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs375272338	chr2:183059890-183059891	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs563823950	chr2:183059894-183059895	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs529517139	chr2:183059951-183059952	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs542836919	chr2:183059959-183059960	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs185201582	chr2:183059960-183059961	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs143315712	chr2:183059984-183059985	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs373665836	chr2:183060085-183060086	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs551400086	chr2:183060089-183060090	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs367568908	chr2:183060093-183060094	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs530511315	chr2:183060097-183060098	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs575119268	chr2:183060125-183060126	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs190018151	chr2:183060126-183060127	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs576161137	chr2:183060198-183060199	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs151165987	chr2:183060209-183060210	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs546446362	chr2:183060254-183060255	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs545060861	chr2:183060257-183060258	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs76135520	chr2:183060346-183060347	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs34758055	chr2:183060368-183060369	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs140319035	chr2:183060454-183060455	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs182703304	chr2:183060457-183060458	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs3769786	chr2:183060460-183060461	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs537025961	chr2:183060461-183060462	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs557668578	chr2:183060490-183060491	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs16822843	chr2:183060510-183060511	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs185835241	chr2:183060557-183060558	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs559645403	chr2:183060591-183060592	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs572984249	chr2:183060598-183060599	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs191619008	chr2:183060614-183060615	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs369820702	chr2:183060640-183060641	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs149921258	chr2:183060647-183060648	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs183869615	chr2:183060752-183060753	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs188872970	chr2:183060797-183060798	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs550291985	chr2:183060803-183060804	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs369253763	chr2:183060868-183060869	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs561255586	chr2:183061091-183061092	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs529921253	chr2:183061110-183061111	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs73975401	chr2:183061198-183061199	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs566367727	chr2:183061260-183061261	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs538441353	chr2:183061264-183061265	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs190909477	chr2:183061286-183061287	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs142221359	chr2:183061288-183061289	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs539989976	chr2:183061397-183061398	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs571390481	chr2:183061428-183061429	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs543587788	chr2:183061440-183061441	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:62)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Ependymoma	16718352	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	18522746	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Testicular germ cell tumor	18059402	CNVD
Breast cancer	16272173	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
Colorectal cancer	16272173	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Lung cancer	18438408	CNVD
Glioblastoma	21080181	CNVD
Prostate cancer	18632612	CNVD
Acute myeloid leukemia	20729466	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
small cell lung cancer	20016488	CNVD
Facial dysmorphism	20548289	CNVD
Mental retardation	20548289	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Cancer	21183584	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Sudden cardiac death	19188705	CNVD
Autism	19329560	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD

Chromatin state (count:2142 , 50 per page) page: 1 2 3 4 5 6 7 ... 43

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:183048400-183073000	Weak transcription	Fetal Stomach	stomach
2	chr2:183048800-183060000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
3	chr2:183050800-183065000	Weak transcription	Aorta	Aorta
4	chr2:183052200-183065000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr2:183052400-183060200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr2:183056400-183065000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
7	chr2:183058800-183065200	Weak transcription	Primary hematopoietic stem cells	blood
8	chr2:183060000-183060800	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
9	chr2:183060200-183061000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
10	chr2:183060600-183065000	Weak transcription	Duodenum Smooth Muscle	Duodenum
11	chr2:183060800-183065000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
12	chr2:183060800-183067200	Weak transcription	Fetal Brain Female	brain
13	chr2:183061000-183065000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
14	chr2:183061000-183085000	Weak transcription	Brain Cingulate Gyrus	brain
15	chr2:183062800-183067000	Weak transcription	Brain Hippocampus Middle	brain
16	chr2:183064200-183066400	Weak transcription	Fetal Muscle Leg	muscle
17	chr2:183064200-183067000	Weak transcription	Right Ventricle	heart
18	chr2:183065000-183065200	Genic enhancers	Aorta	Aorta
19	chr2:183065000-183065800	Strong transcription	Duodenum Smooth Muscle	Duodenum
20	chr2:183065000-183066200	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
21	chr2:183065000-183066600	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
22	chr2:183065000-183067000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chr2:183065000-183067600	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
24	chr2:183065200-183065800	Strong transcription	Aorta	Aorta
25	chr2:183065200-183066000	Strong transcription	Primary hematopoietic stem cells	blood
26	chr2:183065400-183065600	Enhancers	Brain Germinal Matrix	brain
27	chr2:183065800-183087600	Weak transcription	Aorta	Aorta
28	chr2:183065800-183087600	Weak transcription	Duodenum Smooth Muscle	Duodenum
29	chr2:183066000-183066400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
30	chr2:183066000-183068200	Weak transcription	Primary hematopoietic stem cells	blood
31	chr2:183066200-183074800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
32	chr2:183066600-183069800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
33	chr2:183067000-183084000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
34	chr2:183067600-183071200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
35	chr2:183069800-183071600	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
36	chr2:183071200-183071600	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
37	chr2:183071600-183073200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
38	chr2:183071600-183086800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
39	chr2:183072000-183072800	Enhancers	H9 Cell Line	embryonic stem cell
40	chr2:183072000-183072800	Enhancers	iPS-15b Cell Line	embryonic stem cell
41	chr2:183072200-183072400	Enhancers	GM12878-XiMat	blood
42	chr2:183072400-183072800	Enhancers	H1 Cell Line	embryonic stem cell
43	chr2:183072400-183072800	Flanking Active TSS	GM12878-XiMat	blood
44	chr2:183072600-183072800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
45	chr2:183072600-183073000	Enhancers	HUES6 Cell Line	embryonic stem cell
46	chr2:183072800-183073400	Enhancers	GM12878-XiMat	blood
47	chr2:183072800-183076600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
48	chr2:183073000-183073400	Strong transcription	Fetal Stomach	stomach
49	chr2:183073200-183075000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
50	chr2:183073400-183074200	Weak transcription	Fetal Stomach	stomach

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