Variant report

Variant	nsv1013658
Chromosome Location	chr2:211447246-211809945
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:211537752-211538123	HepG2	liver:	n/a	n/a
2	ARID3A	chr2:211763832-211764099	HepG2	liver:	n/a	n/a
3	ARID3A	chr2:211683069-211683350	HepG2	liver:	n/a	n/a
4	ARID3A	chr2:211551150-211551337	HepG2	liver:	n/a	n/a
5	ARID3A	chr2:211482056-211482839	HepG2	liver:	n/a	n/a
6	ARID3A	chr2:211527285-211527735	HepG2	liver:	n/a	n/a
7	ATF2	chr2:211485176-211485680	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF2	chr2:211485262-211485628	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr2:211554831-211554832	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr2:211711877-211711882	H1-hESC	embryonic stem cell:	n/a	n/a
11	BATF	chr2:211491592-211491909	GM12878	blood:	n/a	n/a
12	BATF	chr2:211491610-211491848	GM12878	blood:	n/a	n/a
13	BATF	chr2:211586881-211587076	GM12878	blood:	n/a	n/a
14	BCL11A	chr2:211491609-211491956	GM12878	blood:	n/a	n/a
15	BCL11A	chr2:211485312-211485573	H1-hESC	embryonic stem cell:	n/a	n/a
16	BCL11A	chr2:211777520-211777739	GM12878	blood:	n/a	n/a
17	BCL11A	chr2:211485348-211485556	H1-hESC	embryonic stem cell:	n/a	n/a
18	BCL3	chr2:211668046-211668296	GM12878	blood:	n/a	n/a
19	BCL3	chr2:211667959-211668363	GM12878	blood:	n/a	n/a
20	BHLHE40	chr2:211482623-211482800	GM12878	blood:	n/a	n/a
21	BRCA1	chr2:211583593-211583625	Hela-S3	cervix:	n/a	n/a
22	BRCA1	chr2:211619752-211619828	Hela-S3	cervix:	n/a	n/a
23	CBX3	chr2:211449441-211450072	HCT-116	colon:	n/a	n/a
24	CBX3	chr2:211763857-211764342	HCT-116	colon:	n/a	n/a
25	CCNT2	chr2:211499992-211500187	K562	blood:	n/a	n/a
26	CEBPB	chr2:211536528-211536844	A549	lung:	n/a	chr2:211536688-211536699
27	CEBPB	chr2:211581774-211581974	A549	lung:	n/a	chr2:211581849-211581860 chr2:211581847-211581858 chr2:211581847-211581860
28	CEBPB	chr2:211528336-211528631	HepG2	liver:	n/a	chr2:211528488-211528499 chr2:211528487-211528500 chr2:211528487-211528498
29	CEBPB	chr2:211482106-211482396	A549	lung:	n/a	chr2:211482216-211482229 chr2:211482235-211482246 chr2:211482218-211482229 chr2:211482216-211482227
30	CEBPB	chr2:211587160-211587375	IMR90	lung:	n/a	n/a
31	CEBPB	chr2:211652744-211653060	HepG2	liver:	n/a	chr2:211652876-211652887
32	CEBPB	chr2:211450279-211450534	A549	lung:	n/a	chr2:211450391-211450402
33	CEBPB	chr2:211485251-211485626	H1-hESC	embryonic stem cell:	n/a	chr2:211485430-211485441
34	CEBPB	chr2:211482076-211482307	H1-hESC	embryonic stem cell:	n/a	chr2:211482216-211482229 chr2:211482235-211482246 chr2:211482218-211482229 chr2:211482216-211482227
35	CEBPB	chr2:211485196-211485604	ECC-1	luminal epithelium:	n/a	chr2:211485430-211485441
36	CEBPB	chr2:211467844-211468099	A549	lung:	n/a	chr2:211467976-211467987
37	CEBPB	chr2:211528361-211528602	K562	blood:	n/a	chr2:211528488-211528499 chr2:211528487-211528500 chr2:211528487-211528498
38	CEBPB	chr2:211499909-211500501	HCT-116	colon:	n/a	chr2:211500176-211500187
39	CEBPB	chr2:211586997-211587345	HepG2	liver:	n/a	chr2:211587116-211587133
40	CEBPB	chr2:211528346-211528628	A549	lung:	n/a	chr2:211528488-211528499 chr2:211528487-211528500 chr2:211528487-211528498
41	CEBPB	chr2:211485290-211485581	IMR90	lung:	n/a	chr2:211485430-211485441
42	CEBPB	chr2:211588286-211588498	IMR90	lung:	n/a	chr2:211588368-211588377 chr2:211588368-211588377 chr2:211588366-211588377 chr2:211588368-211588377 chr2:211588368-211588377
43	CEBPB	chr2:211485312-211485539	ECC-1	luminal epithelium:	n/a	chr2:211485430-211485441
44	CEBPB	chr2:211482059-211482790	Hela-S3	cervix:	n/a	chr2:211482216-211482229 chr2:211482235-211482246 chr2:211482218-211482229 chr2:211482216-211482227
45	CEBPB	chr2:211716179-211716281	K562	blood:	n/a	chr2:211716228-211716241 chr2:211716228-211716239 chr2:211716228-211716241 chr2:211716229-211716240 chr2:211716228-211716241
46	CEBPB	chr2:211450219-211450569	IMR90	lung:	n/a	chr2:211450391-211450402
47	CEBPB	chr2:211716120-211716293	Hela-S3	cervix:	n/a	chr2:211716228-211716241 chr2:211716228-211716239 chr2:211716228-211716241 chr2:211716229-211716240 chr2:211716228-211716241
48	CEBPB	chr2:211528229-211528700	MCF-7	breast:	n/a	chr2:211528488-211528499 chr2:211528487-211528500 chr2:211528487-211528498
49	CEBPB	chr2:211499906-211500483	HCT-116	colon:	n/a	chr2:211500176-211500187
50	CEBPB	chr2:211496353-211496534	HepG2	liver:	n/a	chr2:211496409-211496422 chr2:211496410-211496421

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:211503272-211503322	HUVEC	blood vessel:	n/a
2	chr2:211503272-211503322	HUVEC	blood vessel:	n/a
3	chr2:211458173-211458223	Jurkat	blood:	n/a
4	chr2:211457661-211457711	H1-hESC	embryonic stem cell:	embryo
5	chr2:211539520-211539570	HPAEpiC	pulmonary alveolar:	n/a
6	chr2:211457684-211457734	NH-A	brain:	n/a
7	chr2:211480881-211480931	SK-N-SH_RA	brain:	n/a
8	chr2:211457661-211457711	HRE	kidney:	n/a
9	chr2:211458173-211458223	HCF	heart:	n/a
10	chr2:211503272-211503322	HRCEpiC	kidney:	n/a
11	chr2:211457684-211457734	NB4	blood:	n/a
12	chr2:211458173-211458223	GM12891	blood:	n/a
13	chr2:211457684-211457734	BE2_C	brain:	n/a
14	chr2:211480881-211480931	CMK	blood:	n/a
15	chr2:211698619-211698669	HCM	heart:	n/a
16	chr2:211633248-211633298	K562	blood:	n/a
17	chr2:211457661-211457711	NH-A	brain:	n/a
18	chr2:211457684-211457734	HCM	heart:	n/a
19	chr2:211698619-211698669	AG04450	lung:	fetal
20	chr2:211480881-211480931	PANC-1	pancreas:	n/a
21	chr2:211633248-211633298	T-47D	breast:	n/a
22	chr2:211698619-211698669	HCF	heart:	n/a
23	chr2:211458173-211458223	SK-N-SH	brain:	n/a
24	chr2:211457661-211457711	HMEC	breast:	n/a
25	chr2:211698619-211698669	SAEC	small airway:	n/a
26	chr2:211458173-211458223	T-47D	breast:	n/a
27	chr2:211539520-211539570	GM06990	blood:	n/a
28	chr2:211480881-211480931	HRPEpiC	eye:	n/a
29	chr2:211457661-211457711	BE2_C	brain:	n/a
30	chr2:211457661-211457711	Hepatocyte	liver:	n/a
31	chr2:211457632-211457682	HCF	heart:	n/a
32	chr2:211503272-211503322	PrEC	prostate:	n/a
33	chr2:211457684-211457734	GM12892	blood:	n/a
34	chr2:211633248-211633298	HPAEpiC	pulmonary alveolar:	n/a
35	chr2:211539520-211539570	CMK	blood:	n/a
36	chr2:211458173-211458223	SAEC	small airway:	n/a
37	chr2:211503272-211503322	AoSMC	blood vessel:	n/a
38	chr2:211503272-211503322	BJ	skin:	n/a
39	chr2:211583084-211583134	HNPCEpiC	eye:	n/a
40	chr2:211457632-211457682	Caco-2	colon:	n/a
41	chr2:211457632-211457682	BE2_C	brain:	n/a
42	chr2:211633248-211633298	AG04450	lung:	fetal
43	chr2:211633248-211633298	LNCaP	prostate:	n/a
44	chr2:211457632-211457682	GM12878	blood:	n/a
45	chr2:211503272-211503322	NHDF-neo	bronchial:	n/a
46	chr2:211698619-211698669	ovcar-3	ovarian:	n/a
47	chr2:211698619-211698669	NB4	blood:	n/a
48	chr2:211458173-211458223	HRPEpiC	eye:	n/a
49	chr2:211539520-211539570	GM12892	blood:	n/a
50	chr2:211633248-211633298	MCF10A-Er-Src	breast:	n/a

No.	Distal block	Cell Line	Cell type
1	chr2:211527997..211528722-chr2:211900005..211900896,3	MCF-7	breast:
2	chr16:28303287..28304241-chr2:211454910..211455754,2	Hela-S3	cervix:
3	chr2:211644357..211645963-chr2:211649245..211651246,2	K562	blood:
4	chr2:211418752..211420614-chr2:211460883..211463158,2	K562	blood:
5	chr2:211676043..211678802-chr2:211682762..211685242,2	K562	blood:
6	chr2:211528012..211528782-chr2:211919888..211920455,2	MCF-7	breast:
7	chr2:211464829..211466869-chr2:211468442..211470254,2	K562	blood:
8	chr1:17231485..17232131-chr2:211669767..211670267,2	Hela-S3	cervix:
9	chr2:211445309..211447791-chr2:211449881..211452875,2	K562	blood:
10	chr2:211527941..211528689-chr2:211896794..211897496,2	MCF-7	breast:
11	chr2:211450478..211451106-chr9:133320328..133320938,2	Hela-S3	cervix:
12	chr17:57922098..57924197-chr2:211699892..211701526,2	MCF-7	breast:
13	chr2:211593761..211595532-chr2:211597006..211598681,2	K562	blood:
14	chr2:211499410..211501155-chr2:211508100..211509964,2	K562	blood:
15	chr2:211676043..211678802-chr2:211682762..211685242,2	K562	blood:
16	chr17:2627134..2627645-chr2:211447565..211448552,2	Hela-S3	cervix:
17	chr2:211482589..211483492-chr2:211899977..211900599,3	MCF-7	breast:
18	chr12:33049273..33050205-chr2:211482033..211482963,2	Hela-S3	cervix:
19	chr2:211499410..211501155-chr2:211508100..211509964,2	K562	blood:
20	chr1:17231812..17233115-chr2:211669787..211670787,3	HCT-116	colon:
21	chr2:211669822..211672544-chr2:211673084..211674833,2	K562	blood:
22	chr2:211527960..211528912-chr2:211899983..211901271,6	MCF-7	breast:
23	chr2:211309754..211310533-chr2:211481854..211482775,2	MCF-7	breast:
24	chr2:211445309..211447791-chr2:211449881..211452875,2	K562	blood:
25	chr2:211482310..211483112-chr2:212022669..212023186,2	MCF-7	breast:
26	chr2:211644357..211645963-chr2:211649245..211651246,2	K562	blood:
27	chr2:211593761..211595532-chr2:211597006..211598681,2	K562	blood:
28	chr2:211669822..211672544-chr2:211673084..211674833,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RPE-12	chr2:211482295-211484599	NONHSAT076682

Variant related genes	Relation type
CPS1	TF binding region
CPS1	CpG island
ENSG00000246465	chromatin interactions
ENSG00000188322	chromatin interactions
ENSG00000057294	chromatin interactions
ENSG00000021826	chromatin interactions
ENSG00000130707	chromatin interactions

Extended variants
information (count: 6985 )
Associated
traits (count: 59 )

Variant overlapped rSNPs/rCNVs (count:6985 , 50 per page) page: 1 2 3 4 5 6 7 ... 140

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs141636576	chr2:211447259-211447260	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs377168306	chr2:211447301-211447302	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs186719380	chr2:211447330-211447331	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs191182348	chr2:211447337-211447338	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs374019321	chr2:211447343-211447344	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs148967126	chr2:211447356-211447357	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs376091629	chr2:211447375-211447376	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs200271955	chr2:211447393-211447394	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs150369462	chr2:211447406-211447407	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs371257645	chr2:211447460-211447461	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs530792143	chr2:211447464-211447465	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs567330720	chr2:211447545-211447546	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs554023740	chr2:211447579-211447580	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs576549158	chr2:211447645-211447646	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs71420802	chr2:211447725-211447726	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs143713295	chr2:211447726-211447727	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs4490117	chr2:211447793-211447794	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs575662479	chr2:211447839-211447840	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs184022110	chr2:211447846-211447847	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs562058616	chr2:211447847-211447848	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs188571991	chr2:211447859-211447860	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs547572459	chr2:211447902-211447903	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs561043909	chr2:211447925-211447926	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs111835944	chr2:211447926-211447927	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs532670438	chr2:211447927-211447928	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs552731709	chr2:211447947-211447948	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs28499505	chr2:211447950-211447951	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs151023633	chr2:211447970-211447971	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs193020053	chr2:211447979-211447980	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs546667948	chr2:211447984-211447985	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs183047948	chr2:211448019-211448020	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs568736923	chr2:211448021-211448022	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs370056362	chr2:211448063-211448064	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs534195969	chr2:211448069-211448070	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs140947052	chr2:211448071-211448072	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs577058649	chr2:211448144-211448145	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs539625423	chr2:211448162-211448163	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs555889423	chr2:211448165-211448166	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs373074741	chr2:211448200-211448201	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs150261939	chr2:211448214-211448215	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs541818847	chr2:211448374-211448375	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs368129330	chr2:211448403-211448404	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs113633246	chr2:211448423-211448424	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs372052754	chr2:211448448-211448449	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs538744930	chr2:211448503-211448504	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs375979063	chr2:211448519-211448520	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs550124949	chr2:211448572-211448573	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs572328437	chr2:211448582-211448583	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs540935683	chr2:211448583-211448584	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs559032835	chr2:211448607-211448608	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:59)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Ependymoma	16718352	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	17603634	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
Lung cancer	18438408	CNVD
Prostate cancer	18632612	CNVD
Acute myeloid leukemia	20729466	CNVD
small cell lung cancer	20016488	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
Urothelial carcinoma	21177765	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Cervical cancer	21062161	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Non-small cell lung cancer	21829676	CNVD
Autism	20808228	CNVD
Renal cell carcinoma	18765545	CNVD
Ovarian cancer	19193619	CNVD
Non-small cell lung cancer	18676828	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Chordoma	18071362	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	18923514	CNVD
Schizophrenia	22241247	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Urothelial cell carcinoma	18451213	CNVD
Developmental delay	21147756	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Bipolar disorder	19114987	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Schizophrenia	21346763	CNVD

Chromatin state (count:674 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:211435200-211448200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
2	chr2:211435800-211447400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
3	chr2:211438400-211459600	Weak transcription	Small Intestine	intestine
4	chr2:211440400-211448000	Weak transcription	Aorta	Aorta
5	chr2:211442400-211484200	Weak transcription	Duodenum Smooth Muscle	Duodenum
6	chr2:211442800-211477800	Strong transcription	Liver	Liver
7	chr2:211444400-211449400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr2:211444800-211449000	Strong transcription	Duodenum Mucosa	Duodenum
9	chr2:211444800-211449400	Weak transcription	Left Ventricle	heart
10	chr2:211446000-211449600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
11	chr2:211446400-211448000	Weak transcription	Ovary	ovary
12	chr2:211447000-211448000	Strong transcription	Hela-S3	cervix
13	chr2:211447000-211450000	Genic enhancers	Fetal Intestine Large	intestine
14	chr2:211447200-211447400	Enhancers	Fetal Intestine Small	intestine
15	chr2:211447400-211448400	Genic enhancers	Fetal Intestine Small	intestine
16	chr2:211447400-211448800	Strong transcription	Breast Myoepithelial Primary Cells	Breast
17	chr2:211447600-211448600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
18	chr2:211448000-211448600	Strong transcription	Aorta	Aorta
19	chr2:211448000-211448800	Strong transcription	Ovary	ovary
20	chr2:211448000-211449600	Genic enhancers	Hela-S3	cervix
21	chr2:211448200-211448400	ZNF genes & repeats	H9 Derived Neuron Cultured Cells	ES cell derived
22	chr2:211448400-211449000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
23	chr2:211448400-211450000	Enhancers	Fetal Intestine Small	intestine
24	chr2:211448600-211480800	Weak transcription	Aorta	Aorta
25	chr2:211448800-211460200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
26	chr2:211448800-211475400	Weak transcription	Ovary	ovary
27	chr2:211449000-211450200	Weak transcription	Duodenum Mucosa	Duodenum
28	chr2:211449000-211450800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
29	chr2:211449400-211449800	Enhancers	ES-I3 Cell Line	embryonic stem cell
30	chr2:211449400-211449800	Enhancers	iPS-18 Cell Line	embryonic stem cell
31	chr2:211449400-211450000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr2:211449400-211450000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
33	chr2:211449400-211450000	Enhancers	HepG2	liver
34	chr2:211449600-211449800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
35	chr2:211449600-211449800	Weak transcription	Hela-S3	cervix
36	chr2:211449800-211458200	Strong transcription	Hela-S3	cervix
37	chr2:211449800-211467000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
38	chr2:211450000-211451200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
39	chr2:211450000-211454400	Weak transcription	Fetal Intestine Small	intestine
40	chr2:211450000-211457600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
41	chr2:211450000-211458600	Strong transcription	Fetal Intestine Large	intestine
42	chr2:211450000-211466800	Weak transcription	HepG2	liver
43	chr2:211450200-211481400	Strong transcription	Duodenum Mucosa	Duodenum
44	chr2:211450800-211456600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
45	chr2:211451200-211451400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
46	chr2:211451800-211455600	Weak transcription	Left Ventricle	heart
47	chr2:211452200-211452800	Enhancers	Rectal Mucosa Donor 31	rectum
48	chr2:211452400-211452800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
49	chr2:211454400-211455000	Strong transcription	Fetal Intestine Small	intestine
50	chr2:211455000-211457200	Weak transcription	Fetal Intestine Small	intestine

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