Variant report

Variant	nsv870023
Chromosome Location	chr2:178545623-178581407
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:366)
CpG islands
(count:62)
Chromatin interactive
region (count:37)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:366 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:178547107-178547190	K562	blood:	n/a	n/a
2	ARID3A	chr2:178547733-178547776	K562	blood:	n/a	n/a
3	ARID3A	chr2:178557491-178557668	K562	blood:	n/a	n/a
4	ARID3A	chr2:178554400-178554623	K562	blood:	n/a	n/a
5	ARID3A	chr2:178548061-178548261	K562	blood:	n/a	n/a
6	ARID3A	chr2:178556633-178557685	HepG2	liver:	n/a	n/a
7	ARID3A	chr2:178558288-178559366	K562	blood:	n/a	n/a
8	ARID3A	chr2:178545962-178546169	K562	blood:	n/a	n/a
9	ATF1	chr2:178554407-178554764	K562	blood:	n/a	n/a
10	ATF1	chr2:178577274-178577463	K562	blood:	n/a	n/a
11	ATF1	chr2:178558560-178559091	K562	blood:	n/a	n/a
12	ATF3	chr2:178558359-178559087	K562	blood:	n/a	n/a
13	BACH1	chr2:178546276-178546278	K562	blood:	n/a	n/a
14	BHLHE40	chr2:178558039-178559104	K562	blood:	n/a	n/a
15	BHLHE40	chr2:178557739-178557741	K562	blood:	n/a	n/a
16	BHLHE40	chr2:178554454-178554631	K562	blood:	n/a	n/a
17	BHLHE40	chr2:178548418-178548511	K562	blood:	n/a	n/a
18	BHLHE40	chr2:178547831-178548018	K562	blood:	n/a	n/a
19	CCNT2	chr2:178547689-178547927	K562	blood:	n/a	n/a
20	CCNT2	chr2:178558442-178559135	K562	blood:	n/a	chr2:178558864-178558884
21	CCNT2	chr2:178554360-178554689	K562	blood:	n/a	n/a
22	CEBPB	chr2:178557275-178557602	A549	lung:	n/a	chr2:178557583-178557595
23	CEBPB	chr2:178557191-178557717	A549	lung:	n/a	chr2:178557583-178557595
24	CEBPB	chr2:178557271-178557521	Hela-S3	cervix:	n/a	n/a
25	CEBPB	chr2:178577175-178577479	K562	blood:	n/a	chr2:178577372-178577383
26	CEBPB	chr2:178577294-178577521	K562	blood:	n/a	chr2:178577372-178577383
27	CEBPB	chr2:178581281-178581519	HepG2	liver:	n/a	chr2:178581417-178581428 chr2:178581417-178581430 chr2:178581419-178581428 chr2:178581418-178581429
28	CEBPB	chr2:178549557-178549765	HepG2	liver:	n/a	chr2:178549681-178549692
29	CEBPB	chr2:178551012-178551128	IMR90	lung:	n/a	chr2:178551070-178551081
30	CEBPB	chr2:178550913-178551154	K562	blood:	n/a	chr2:178551070-178551081
31	CEBPB	chr2:178550933-178551169	HepG2	liver:	n/a	chr2:178551070-178551081
32	CEBPB	chr2:178558416-178558685	IMR90	lung:	n/a	chr2:178558576-178558587
33	CEBPB	chr2:178549634-178549761	K562	blood:	n/a	chr2:178549681-178549692
34	CEBPB	chr2:178557263-178557501	HepG2	liver:	n/a	n/a
35	CEBPB	chr2:178558425-178559027	K562	blood:	n/a	chr2:178558576-178558587
36	CEBPB	chr2:178569543-178569609	HepG2	liver:	n/a	chr2:178569565-178569576
37	CEBPB	chr2:178550933-178551144	A549	lung:	n/a	chr2:178551070-178551081
38	CEBPB	chr2:178558429-178558729	A549	lung:	n/a	chr2:178558576-178558587
39	CEBPB	chr2:178558399-178559087	K562	blood:	n/a	chr2:178558576-178558587
40	CEBPB	chr2:178558415-178558716	HepG2	liver:	n/a	chr2:178558576-178558587
41	CEBPB	chr2:178558569-178558614	H1-hESC	embryonic stem cell:	n/a	chr2:178558576-178558587
42	CEBPB	chr2:178581271-178581550	K562	blood:	n/a	chr2:178581417-178581428 chr2:178581417-178581430 chr2:178581419-178581428 chr2:178581418-178581429
43	CEBPB	chr2:178558315-178559143	K562	blood:	n/a	chr2:178558576-178558587
44	CEBPB	chr2:178581263-178581586	IMR90	lung:	n/a	chr2:178581417-178581428 chr2:178581417-178581430 chr2:178581419-178581428 chr2:178581418-178581429
45	CEBPB	chr2:178557240-178557599	HepG2	liver:	n/a	chr2:178557583-178557595
46	CEBPB	chr2:178550983-178551107	H1-hESC	embryonic stem cell:	n/a	chr2:178551070-178551081
47	CEBPD	chr2:178558362-178559103	K562	blood:	n/a	n/a
48	CEBPD	chr2:178558470-178559144	K562	blood:	n/a	n/a
49	CTCF	chr2:178556120-178556270	GM12869	blood:	n/a	n/a
50	CTCF	chr2:178557634-178557805	A549	lung:	n/a	n/a

(count:62 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:178556488-178556538	AG04449	skin:	fetal
2	chr2:178556488-178556538	AG04449	skin:	fetal
3	chr2:178556488-178556538	SK-N-MC	brain:	n/a
4	chr2:178556488-178556538	Jurkat	blood:	n/a
5	chr2:178556488-178556538	U87	brain:	n/a
6	chr2:178556488-178556538	K562	blood:	n/a
7	chr2:178556488-178556538	NH-A	brain:	n/a
8	chr2:178556488-178556538	HCF	heart:	n/a
9	chr2:178556488-178556538	GM12891	blood:	n/a
10	chr2:178556488-178556538	SK-N-SH_RA	brain:	n/a
11	chr2:178556488-178556538	MCF10A-Er-Src	breast:	n/a
12	chr2:178556488-178556538	RPTEC	kidney:	n/a
13	chr2:178556488-178556538	NT2-D1	testis:	n/a
14	chr2:178556488-178556538	AG10803	skin:	n/a
15	chr2:178556488-178556538	A549	lung:	n/a
16	chr2:178556488-178556538	AG09309	skin:	n/a
17	chr2:178556488-178556538	PANC-1	pancreas:	n/a
18	chr2:178556488-178556538	PrEC	prostate:	n/a
19	chr2:178556488-178556538	SAEC	small airway:	n/a
20	chr2:178556488-178556538	Hepatocyte	liver:	n/a
21	chr2:178556488-178556538	Caco-2	colon:	n/a
22	chr2:178556488-178556538	HMEC	breast:	n/a
23	chr2:178556488-178556538	BE2_C	brain:	n/a
24	chr2:178556488-178556538	ProgFib	skin:	n/a
25	chr2:178556488-178556538	HRPEpiC	eye:	n/a
26	chr2:178556488-178556538	HAEpiC	amniotic membrane:	n/a
27	chr2:178556488-178556538	GM06990	blood:	n/a
28	chr2:178556488-178556538	HNPCEpiC	eye:	n/a
29	chr2:178556488-178556538	HCPEpiC	choroid plexus:	n/a
30	chr2:178556488-178556538	HEK293	kidney:	embryo
31	chr2:178556488-178556538	IMR90	lung:	fetal
32	chr2:178556488-178556538	GM19239	blood:	n/a
33	chr2:178556488-178556538	NHBE	bronchial:	n/a
34	chr2:178556488-178556538	Hela-S3	cervix:	n/a
35	chr2:178556488-178556538	HCT-116	colon:	n/a
36	chr2:178556488-178556538	AG04450	lung:	fetal
37	chr2:178556488-178556538	CMK	blood:	n/a
38	chr2:178556488-178556538	SKMC	muscle:	n/a
39	chr2:178556488-178556538	HL-60	blood:	n/a
40	chr2:178556488-178556538	HIPEpiC	eye:	n/a
41	chr2:178556488-178556538	BJ	skin:	n/a
42	chr2:178556488-178556538	HPAEpiC	pulmonary alveolar:	n/a
43	chr2:178556488-178556538	GM12878	blood:	n/a
44	chr2:178556488-178556538	NHDF-neo	bronchial:	n/a
45	chr2:178556488-178556538	H1-hESC	embryonic stem cell:	embryo
46	chr2:178556488-178556538	HRE	kidney:	n/a
47	chr2:178556488-178556538	HCM	heart:	n/a
48	chr2:178556488-178556538	SK-N-SH	brain:	n/a
49	chr2:178556488-178556538	HepG2	liver:	n/a
50	chr2:178556488-178556538	T-47D	breast:	n/a

(count:37 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:178570926..178572812-chr2:178573756..178576490,2	K562	blood:
2	chr2:178556581..178559111-chr2:178571009..178573713,2	K562	blood:
3	chr2:178573812..178575590-chr2:178578150..178581099,2	K562	blood:
4	chr2:178557613..178559704-chr2:178561778..178563487,2	K562	blood:
5	chr2:178556581..178559111-chr2:178571009..178573713,2	K562	blood:
6	chr2:178559293..178562880-chr2:178620510..178622541,4	K562	blood:
7	chr2:178546208..178548509-chr2:178552748..178555951,3	K562	blood:
8	chr2:178567581..178570235-chr2:178573899..178577717,4	K562	blood:
9	chr2:178568725..178571101-chr2:178581270..178584257,2	K562	blood:
10	chr2:178416053..178418708-chr2:178570239..178572777,3	MCF-7	breast:
11	chr2:178563706..178566606-chr2:178575234..178578088,2	K562	blood:
12	chr2:178560703..178563309-chr2:178574867..178577003,2	K562	blood:
13	chr2:178257363..178259725-chr2:178564767..178567324,2	K562	blood:
14	chr2:178573812..178575590-chr2:178578150..178581099,2	K562	blood:
15	chr2:178557827..178560384-chr2:178566181..178567818,2	K562	blood:
16	chr2:178563706..178566606-chr2:178575234..178578088,2	K562	blood:
17	chr2:178540518..178542600-chr2:178544661..178547619,2	MCF-7	breast:
18	chr2:178554622..178556769-chr2:178559553..178561777,2	K562	blood:
19	chr2:178553724..178556122-chr2:178557669..178561053,4	K562	blood:
20	chr2:178561119..178564111-chr2:178566483..178568629,4	K562	blood:
21	chr2:178454525..178456445-chr2:178573217..178575511,2	K562	blood:
22	chr2:178562301..178565158-chr2:178568749..178571184,2	K562	blood:
23	chr2:178536377..178538004-chr2:178556463..178558808,2	K562	blood:
24	chr2:178570926..178572812-chr2:178573756..178576490,2	K562	blood:
25	chr2:178554622..178556769-chr2:178559553..178561777,2	K562	blood:
26	chr2:178553724..178556122-chr2:178557669..178561053,4	K562	blood:
27	chr2:178568725..178571101-chr2:178581270..178584257,2	K562	blood:
28	chr2:178561207..178563093-chr2:178570078..178571660,2	MCF-7	breast:
29	chr2:178557827..178560384-chr2:178566181..178567818,2	K562	blood:
30	chr2:178578841..178579788-chr2:178589264..178590054,2	K562	blood:
31	chr2:178562301..178564741-chr2:178568694..178570249,2	K562	blood:
32	chr2:178567581..178570235-chr2:178573899..178577717,4	K562	blood:
33	chr2:178561207..178563093-chr2:178570078..178571660,2	MCF-7	breast:
34	chr2:178406208..178409033-chr2:178580578..178582428,2	K562	blood:
35	chr2:178579061..178582012-chr2:178598447..178601260,2	K562	blood:
36	chr2:178561612..178563811-chr2:178565917..178568583,4	K562	blood:
37	chr2:178577863..178580571-chr2:178582573..178585584,3	K562	blood:

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AGPS-3	chr2:178565822-178565956	ENSG00000229941.1
2	lnc-AGPS-3	chr2:178567216-178567477	ENSG00000229941.1
3	lnc-AGPS-3	chr2:178563157-178563299	ENSG00000229941.1
4	lnc-AGPS-3	chr2:178567216-178567477	ENSG00000229941.1
5	lnc-AGPS-3	chr2:178563218-178563299	ENSG00000229941.1

No data

Variant related genes	Relation type
ENSG00000229941	TF binding region
PDE11A	TF binding region
ENSG00000229941	CpG island
PDE11A	CpG island
ENSG00000213963	chromatin interactions
ENSG00000196659	chromatin interactions
ENSG00000116044	chromatin interactions
ENSG00000229941	chromatin interactions
ENSG00000018510	chromatin interactions
ENSG00000128655	chromatin interactions

Extended variants
information (count: 1388 )
Associated
traits (count: 50 )

Variant overlapped rSNPs/rCNVs (count:1388 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs200101345	chr2:178545623-178545624	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs370449746	chr2:178545630-178545631	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs368459280	chr2:178545638-178545639	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs374356377	chr2:178545660-178545661	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs11304036	chr2:178545661-178545662	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs146153854	chr2:178545664-178545665	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs4538242	chr2:178545713-178545714	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs9677333	chr2:178545736-178545737	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs189262283	chr2:178545860-178545861	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs376848715	chr2:178545896-178545897	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs9679360	chr2:178545898-178545899	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs572284471	chr2:178545926-178545927	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs9288008	chr2:178545934-178545935	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs558086455	chr2:178546005-178546006	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs9677970	chr2:178546016-178546017	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs543492408	chr2:178546036-178546037	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs546110874	chr2:178546042-178546043	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs553609171	chr2:178546048-178546049	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs192896340	chr2:178546138-178546139	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs184921641	chr2:178546172-178546173	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs200604042	chr2:178546184-178546185	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs112479225	chr2:178546185-178546186	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs58944470	chr2:178546188-178546189	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs543190878	chr2:178546237-178546238	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs542400543	chr2:178546238-178546239	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs561678312	chr2:178546240-178546241	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs11901771	chr2:178546260-178546261	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs551613423	chr2:178546276-178546277	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs60295960	chr2:178546302-178546303	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs189375165	chr2:178546327-178546328	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs180772110	chr2:178546439-178546440	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs569714502	chr2:178546463-178546464	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs78778808	chr2:178546475-178546476	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs11901841	chr2:178546479-178546480	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs138871813	chr2:178546482-178546483	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs564086563	chr2:178546518-178546519	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs532926401	chr2:178546553-178546554	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs11891283	chr2:178546554-178546555	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs558074044	chr2:178546568-178546569	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs10803914	chr2:178546573-178546574	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs12466205	chr2:178546596-178546597	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs185147787	chr2:178546611-178546612	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs573994942	chr2:178546694-178546695	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs542686362	chr2:178546696-178546697	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs559424971	chr2:178546731-178546732	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs528624273	chr2:178546750-178546751	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs545240461	chr2:178546825-178546826	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs565237329	chr2:178546840-178546841	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs75667657	chr2:178546986-178546987	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs551268509	chr2:178546987-178546988	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:50)

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
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
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
Invasive pancreatic ductal carcinoma	16982739	CNVD
Prostate cancer	18632612	CNVD
Sudden cardiac death	19188705	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21364760	CNVD
Ovarian cancer	21720365	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
small cell lung cancer	20016488	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	18923514	CNVD
Schizophrenia	22241247	CNVD
Mental retardation	21062444	CNVD
Facial dysmorphism	20548289	CNVD
Mental retardation	20548289	CNVD
Schizophrenia	19348701	CNVD
Muscular dystrophy	17160897	CNVD
Cardiomyopathy	17576883	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:178536600-178556000	Weak transcription	Pancreas	Pancrea
2	chr2:178540000-178547400	Enhancers	Fetal Kidney	kidney
3	chr2:178543400-178546400	Enhancers	Rectal Mucosa Donor 31	rectum
4	chr2:178544000-178548000	Enhancers	K562	blood
5	chr2:178544600-178546800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr2:178544600-178552600	Weak transcription	Fetal Intestine Small	intestine
7	chr2:178545000-178547000	Enhancers	Duodenum Mucosa	Duodenum
8	chr2:178545200-178546200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
9	chr2:178545200-178548000	Weak transcription	Adipose Nuclei	Adipose
10	chr2:178545400-178546200	Weak transcription	Small Intestine	intestine
11	chr2:178545400-178549200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
12	chr2:178545800-178546600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
13	chr2:178545800-178547400	Enhancers	iPS-18 Cell Line	embryonic stem cell
14	chr2:178546000-178546400	Enhancers	iPS-20b Cell Line	embryonic stem cell
15	chr2:178546000-178547200	Enhancers	HUES6 Cell Line	embryonic stem cell
16	chr2:178546200-178546400	Enhancers	HUES48 Cell Line	embryonic stem cell
17	chr2:178546200-178546600	Enhancers	Small Intestine	intestine
18	chr2:178546200-178548600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
19	chr2:178546400-178547000	Enhancers	ES-I3 Cell Line	embryonic stem cell
20	chr2:178546400-178547200	Enhancers	H1 Cell Line	embryonic stem cell
21	chr2:178546400-178547200	Enhancers	H9 Cell Line	embryonic stem cell
22	chr2:178546400-178547200	Enhancers	HUES64 Cell Line	embryonic stem cell
23	chr2:178546400-178547200	Enhancers	iPS-15b Cell Line	embryonic stem cell
24	chr2:178546600-178546800	Weak transcription	Small Intestine	intestine
25	chr2:178546800-178547200	Enhancers	Small Intestine	intestine
26	chr2:178546800-178554400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
27	chr2:178547000-178552800	Weak transcription	Duodenum Mucosa	Duodenum
28	chr2:178547200-178548200	Enhancers	HepG2	liver
29	chr2:178547400-178549000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
30	chr2:178547400-178554400	Weak transcription	Fetal Kidney	kidney
31	chr2:178548000-178548600	Enhancers	Adipose Nuclei	Adipose
32	chr2:178548000-178548600	Flanking Active TSS	K562	blood
33	chr2:178548200-178549400	Weak transcription	HepG2	liver
34	chr2:178548600-178549200	Weak transcription	Adipose Nuclei	Adipose
35	chr2:178548600-178549400	Enhancers	K562	blood
36	chr2:178548600-178549600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
37	chr2:178549200-178549400	Enhancers	Adipose Nuclei	Adipose
38	chr2:178549200-178550000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
39	chr2:178549400-178550000	Enhancers	Stomach Mucosa	stomach
40	chr2:178549400-178550200	Enhancers	HepG2	liver
41	chr2:178549400-178554400	Weak transcription	K562	blood
42	chr2:178549600-178550400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
43	chr2:178550000-178554200	Weak transcription	Stomach Mucosa	stomach
44	chr2:178550000-178557000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
45	chr2:178550400-178555800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
46	chr2:178552600-178552800	Enhancers	Sigmoid Colon	Sigmoid Colon
47	chr2:178552600-178553000	Enhancers	Fetal Intestine Small	intestine
48	chr2:178552800-178553000	Enhancers	Fetal Intestine Large	intestine
49	chr2:178552800-178553000	Bivalent Enhancer	Sigmoid Colon	Sigmoid Colon
50	chr2:178552800-178553200	Enhancers	Duodenum Mucosa	Duodenum

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