Variant report

Variant	nsv431812
Chromosome Location	chr2:178525371-178584470
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:794)
CpG islands
(count:62)
Chromatin interactive
region (count:49)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:794 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:178554400-178554623	K562	blood:	n/a	n/a
2	ARID3A	chr2:178531225-178531530	K562	blood:	n/a	n/a
3	ARID3A	chr2:178557491-178557668	K562	blood:	n/a	n/a
4	ARID3A	chr2:178544614-178545268	K562	blood:	n/a	n/a
5	ARID3A	chr2:178547733-178547776	K562	blood:	n/a	n/a
6	ARID3A	chr2:178547107-178547190	K562	blood:	n/a	n/a
7	ARID3A	chr2:178556633-178557685	HepG2	liver:	n/a	n/a
8	ARID3A	chr2:178558288-178559366	K562	blood:	n/a	n/a
9	ARID3A	chr2:178548061-178548261	K562	blood:	n/a	n/a
10	ARID3A	chr2:178545962-178546169	K562	blood:	n/a	n/a
11	ATF1	chr2:178554407-178554764	K562	blood:	n/a	n/a
12	ATF1	chr2:178558560-178559091	K562	blood:	n/a	n/a
13	ATF1	chr2:178577274-178577463	K562	blood:	n/a	n/a
14	ATF1	chr2:178531217-178531450	K562	blood:	n/a	n/a
15	ATF2	chr2:178535607-178535979	GM12878	blood:	n/a	n/a
16	ATF2	chr2:178535601-178536035	H1-hESC	embryonic stem cell:	n/a	n/a
17	ATF2	chr2:178535367-178536047	GM12878	blood:	n/a	n/a
18	ATF3	chr2:178558359-178559087	K562	blood:	n/a	n/a
19	BACH1	chr2:178546276-178546278	K562	blood:	n/a	n/a
20	BHLHE40	chr2:178544674-178545243	K562	blood:	n/a	n/a
21	BHLHE40	chr2:178554454-178554631	K562	blood:	n/a	n/a
22	BHLHE40	chr2:178558039-178559104	K562	blood:	n/a	n/a
23	BHLHE40	chr2:178557739-178557741	K562	blood:	n/a	n/a
24	BHLHE40	chr2:178547831-178548018	K562	blood:	n/a	n/a
25	BHLHE40	chr2:178548418-178548511	K562	blood:	n/a	n/a
26	CCNT2	chr2:178558442-178559135	K562	blood:	n/a	chr2:178558864-178558884
27	CCNT2	chr2:178534089-178534289	K562	blood:	n/a	n/a
28	CCNT2	chr2:178547689-178547927	K562	blood:	n/a	n/a
29	CCNT2	chr2:178554360-178554689	K562	blood:	n/a	n/a
30	CCNT2	chr2:178544654-178545350	K562	blood:	n/a	chr2:178545114-178545134
31	CEBPB	chr2:178550983-178551107	H1-hESC	embryonic stem cell:	n/a	chr2:178551070-178551081
32	CEBPB	chr2:178581281-178581519	HepG2	liver:	n/a	chr2:178581417-178581428 chr2:178581417-178581430 chr2:178581419-178581428 chr2:178581418-178581429
33	CEBPB	chr2:178558416-178558685	IMR90	lung:	n/a	chr2:178558576-178558587
34	CEBPB	chr2:178581271-178581550	K562	blood:	n/a	chr2:178581417-178581428 chr2:178581417-178581430 chr2:178581419-178581428 chr2:178581418-178581429
35	CEBPB	chr2:178549634-178549761	K562	blood:	n/a	chr2:178549681-178549692
36	CEBPB	chr2:178581263-178581586	IMR90	lung:	n/a	chr2:178581417-178581428 chr2:178581417-178581430 chr2:178581419-178581428 chr2:178581418-178581429
37	CEBPB	chr2:178558415-178558716	HepG2	liver:	n/a	chr2:178558576-178558587
38	CEBPB	chr2:178557271-178557521	Hela-S3	cervix:	n/a	n/a
39	CEBPB	chr2:178558315-178559143	K562	blood:	n/a	chr2:178558576-178558587
40	CEBPB	chr2:178557275-178557602	A549	lung:	n/a	chr2:178557583-178557595
41	CEBPB	chr2:178577175-178577479	K562	blood:	n/a	chr2:178577372-178577383
42	CEBPB	chr2:178569543-178569609	HepG2	liver:	n/a	chr2:178569565-178569576
43	CEBPB	chr2:178550933-178551169	HepG2	liver:	n/a	chr2:178551070-178551081
44	CEBPB	chr2:178557191-178557717	A549	lung:	n/a	chr2:178557583-178557595
45	CEBPB	chr2:178550933-178551144	A549	lung:	n/a	chr2:178551070-178551081
46	CEBPB	chr2:178550913-178551154	K562	blood:	n/a	chr2:178551070-178551081
47	CEBPB	chr2:178558429-178558729	A549	lung:	n/a	chr2:178558576-178558587
48	CEBPB	chr2:178549557-178549765	HepG2	liver:	n/a	chr2:178549681-178549692
49	CEBPB	chr2:178557240-178557599	HepG2	liver:	n/a	chr2:178557583-178557595
50	CEBPB	chr2:178577294-178577521	K562	blood:	n/a	chr2:178577372-178577383

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:178556488-178556538	SAEC	small airway:	n/a
2	chr2:178556488-178556538	SAEC	small airway:	n/a
3	chr2:178556488-178556538	HRE	kidney:	n/a
4	chr2:178556488-178556538	CMK	blood:	n/a
5	chr2:178556488-178556538	HCF	heart:	n/a
6	chr2:178556488-178556538	HIPEpiC	eye:	n/a
7	chr2:178556488-178556538	K562	blood:	n/a
8	chr2:178556488-178556538	HAEpiC	amniotic membrane:	n/a
9	chr2:178556488-178556538	HPAEpiC	pulmonary alveolar:	n/a
10	chr2:178556488-178556538	GM12892	blood:	n/a
11	chr2:178556488-178556538	ProgFib	skin:	n/a
12	chr2:178556488-178556538	HNPCEpiC	eye:	n/a
13	chr2:178556488-178556538	PANC-1	pancreas:	n/a
14	chr2:178556488-178556538	HMEC	breast:	n/a
15	chr2:178556488-178556538	GM12878	blood:	n/a
16	chr2:178556488-178556538	Jurkat	blood:	n/a
17	chr2:178556488-178556538	AG10803	skin:	n/a
18	chr2:178556488-178556538	BJ	skin:	n/a
19	chr2:178556488-178556538	GM19239	blood:	n/a
20	chr2:178556488-178556538	A549	lung:	n/a
21	chr2:178556488-178556538	ECC-1	luminal epithelium:	n/a
22	chr2:178556488-178556538	PFSK-1	brain:	n/a
23	chr2:178556488-178556538	AG04450	lung:	fetal
24	chr2:178556488-178556538	SKMC	muscle:	n/a
25	chr2:178556488-178556538	IMR90	lung:	fetal
26	chr2:178556488-178556538	Caco-2	colon:	n/a
27	chr2:178556488-178556538	LNCaP	prostate:	n/a
28	chr2:178556488-178556538	U87	brain:	n/a
29	chr2:178556488-178556538	HEEpiC	esophagus:	n/a
30	chr2:178556488-178556538	GM06990	blood:	n/a
31	chr2:178556488-178556538	GM12891	blood:	n/a
32	chr2:178556488-178556538	NHDF-neo	bronchial:	n/a
33	chr2:178556488-178556538	BE2_C	brain:	n/a
34	chr2:178556488-178556538	HCPEpiC	choroid plexus:	n/a
35	chr2:178556488-178556538	NB4	blood:	n/a
36	chr2:178556488-178556538	PrEC	prostate:	n/a
37	chr2:178556488-178556538	HUVEC	blood vessel:	n/a
38	chr2:178556488-178556538	MCF10A-Er-Src	breast:	n/a
39	chr2:178556488-178556538	AG04449	skin:	fetal
40	chr2:178556488-178556538	SK-N-SH	brain:	n/a
41	chr2:178556488-178556538	HCM	heart:	n/a
42	chr2:178556488-178556538	HEK293	kidney:	embryo
43	chr2:178556488-178556538	NH-A	brain:	n/a
44	chr2:178556488-178556538	AG09309	skin:	n/a
45	chr2:178556488-178556538	HL-60	blood:	n/a
46	chr2:178556488-178556538	Hepatocyte	liver:	n/a
47	chr2:178556488-178556538	HRCEpiC	kidney:	n/a
48	chr2:178556488-178556538	HepG2	liver:	n/a
49	chr2:178556488-178556538	HCT-116	colon:	n/a
50	chr2:178556488-178556538	SK-N-SH_RA	brain:	n/a

(count:49 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:178553724..178556122-chr2:178557669..178561053,4	K562	blood:
2	chr2:178562301..178564741-chr2:178568694..178570249,2	K562	blood:
3	chr2:178567581..178570235-chr2:178573899..178577717,4	K562	blood:
4	chr2:178533626..178535228-chr2:178535564..178538374,2	K562	blood:
5	chr2:178257363..178259725-chr2:178564767..178567324,2	K562	blood:
6	chr2:178557827..178560384-chr2:178566181..178567818,2	K562	blood:
7	chr2:178416053..178418708-chr2:178570239..178572777,3	MCF-7	breast:
8	chr1:67678579..67680079-chr2:178536885..178539298,2	MCF-7	breast:
9	chr2:178570926..178572812-chr2:178573756..178576490,2	K562	blood:
10	chr2:178559293..178562880-chr2:178620510..178622541,4	K562	blood:
11	chr2:178546208..178548509-chr2:178552748..178555951,3	K562	blood:
12	chr2:178561207..178563093-chr2:178570078..178571660,2	MCF-7	breast:
13	chr2:178568725..178571101-chr2:178581270..178584257,2	K562	blood:
14	chr2:178554622..178556769-chr2:178559553..178561777,2	K562	blood:
15	chr2:178556581..178559111-chr2:178571009..178573713,2	K562	blood:
16	chr2:178521915..178523985-chr2:178527127..178529647,2	K562	blood:
17	chr2:178579061..178582012-chr2:178598447..178601260,2	K562	blood:
18	chr2:178554622..178556769-chr2:178559553..178561777,2	K562	blood:
19	chr2:178406208..178409033-chr2:178580578..178582428,2	K562	blood:
20	chr2:178128784..178131655-chr2:178537635..178540049,2	K562	blood:
21	chr2:178573812..178575590-chr2:178578150..178581099,2	K562	blood:
22	chr2:178524145..178525778-chr2:178526454..178528465,2	K562	blood:
23	chr2:178556581..178559111-chr2:178571009..178573713,2	K562	blood:
24	chr2:178553724..178556122-chr2:178557669..178561053,4	K562	blood:
25	chr2:178533626..178535228-chr2:178535564..178538374,2	K562	blood:
26	chr2:178560703..178563309-chr2:178574867..178577003,2	K562	blood:
27	chr2:178568725..178571101-chr2:178581270..178584257,2	K562	blood:
28	chr2:178557827..178560384-chr2:178566181..178567818,2	K562	blood:
29	chr2:178524145..178525778-chr2:178526454..178528465,2	K562	blood:
30	chr2:178536377..178538004-chr2:178556463..178558808,2	K562	blood:
31	chr2:178570926..178572812-chr2:178573756..178576490,2	K562	blood:
32	chr2:178562301..178565158-chr2:178568749..178571184,2	K562	blood:
33	chr2:178536377..178538004-chr2:178556463..178558808,2	K562	blood:
34	chr2:178561612..178563811-chr2:178565917..178568583,4	K562	blood:
35	chr2:178518512..178521543-chr2:178525279..178528697,3	K562	blood:
36	chr2:178577863..178580571-chr2:178582573..178585584,3	K562	blood:
37	chr2:178561119..178564111-chr2:178566483..178568629,4	K562	blood:
38	chr2:178577863..178580571-chr2:178582573..178585584,3	K562	blood:
39	chr2:178567581..178570235-chr2:178573899..178577717,4	K562	blood:
40	chr2:178128784..178131655-chr2:178537635..178541213,3	K562	blood:
41	chr2:178573812..178575590-chr2:178578150..178581099,2	K562	blood:
42	chr2:178454525..178456445-chr2:178573217..178575511,2	K562	blood:
43	chr2:178582201..178583122-chr2:178623256..178624160,2	MCF-7	breast:
44	chr2:178563706..178566606-chr2:178575234..178578088,2	K562	blood:
45	chr2:178540518..178542600-chr2:178544661..178547619,2	MCF-7	breast:
46	chr2:178563706..178566606-chr2:178575234..178578088,2	K562	blood:
47	chr2:178561207..178563093-chr2:178570078..178571660,2	MCF-7	breast:
48	chr2:178557613..178559704-chr2:178561778..178563487,2	K562	blood:
49	chr2:178578841..178579788-chr2:178589264..178590054,2	K562	blood:

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

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

No data

Variant related genes	Relation type
ENSG00000229941	TF binding region
PDE11A	TF binding region
ENSG00000229941	CpG island
PDE11A	CpG island
ENSG00000128655	chromatin interactions
ENSG00000222043	chromatin interactions
ENSG00000018510	chromatin interactions
ENSG00000196659	chromatin interactions
ENSG00000213963	chromatin interactions
ENSG00000229941	chromatin interactions
ENSG00000116044	chromatin interactions

Extended variants
information (count: 2329 )
Associated
traits (count: 51 )

Variant overlapped rSNPs/rCNVs (count:2329 , 50 per page) page: 1 2 3 4 5 6 7 ... 47

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs16865535	chr2:178525371-178525372	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs1527408	chr2:178525389-178525390	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs184377065	chr2:178525398-178525399	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs550470501	chr2:178525399-178525400	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs528034407	chr2:178525411-178525412	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
6	rs149883377	chr2:178525453-178525454	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
7	rs566504166	chr2:178525466-178525467	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
8	rs115175652	chr2:178525478-178525479	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
9	rs532599840	chr2:178525566-178525567	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
10	rs568877954	chr2:178525569-178525570	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
11	rs144875104	chr2:178525577-178525578	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
12	rs554475684	chr2:178525621-178525622	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs1527407	chr2:178525630-178525631	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs528806753	chr2:178525637-178525638	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs1527406	chr2:178525655-178525656	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs11887429	chr2:178525671-178525672	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs376483468	chr2:178525709-178525710	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs562954745	chr2:178525710-178525711	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs111252494	chr2:178525725-178525726	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs368501927	chr2:178525754-178525755	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs1527405	chr2:178525827-178525828	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs375013537	chr2:178525843-178525844	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs190252949	chr2:178525859-178525860	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs568071808	chr2:178525897-178525898	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs541782612	chr2:178525899-178525900	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs181259405	chr2:178525902-178525903	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs73977698	chr2:178525910-178525911	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs141867584	chr2:178525982-178525983	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs185041530	chr2:178526003-178526004	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs557258081	chr2:178526039-178526040	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs147101834	chr2:178526124-178526125	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs7591796	chr2:178526134-178526135	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs372901406	chr2:178526158-178526159	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs7591897	chr2:178526189-178526190	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs567941569	chr2:178526190-178526191	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs533820970	chr2:178526203-178526204	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs553615761	chr2:178526206-178526207	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs570417466	chr2:178526239-178526240	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs77222272	chr2:178526298-178526299	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs556323794	chr2:178526341-178526342	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs75123253	chr2:178526367-178526368	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs541987689	chr2:178526387-178526388	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs573033229	chr2:178526403-178526404	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs555983668	chr2:178526408-178526409	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs374113452	chr2:178526409-178526410	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs373543888	chr2:178526463-178526464	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs572645011	chr2:178526470-178526471	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs189090416	chr2:178526502-178526503	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs564719912	chr2:178526539-178526540	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs533469091	chr2:178526569-178526570	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:51)

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
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:431 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:178517200-178530800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr2:178524000-178525800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr2:178524200-178525800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr2:178524400-178525800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
5	chr2:178524800-178525800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr2:178524800-178532800	Weak transcription	Fetal Kidney	kidney
7	chr2:178524800-178533400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
8	chr2:178525200-178527600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr2:178525400-178525600	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
10	chr2:178525800-178526000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr2:178527400-178527600	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
12	chr2:178527400-178528200	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
13	chr2:178527600-178528600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr2:178527600-178528600	Enhancers	Cortex derived primary cultured neurospheres	brain
15	chr2:178527600-178528600	Enhancers	Brain Inferior Temporal Lobe	brain
16	chr2:178527800-178528000	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
17	chr2:178527800-178528000	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
18	chr2:178528600-178534000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr2:178530800-178531000	Enhancers	K562	blood
20	chr2:178530800-178531200	Enhancers	HSMM	muscle
21	chr2:178530800-178531400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
22	chr2:178530800-178531400	Enhancers	Hela-S3	cervix
23	chr2:178530800-178531600	Enhancers	Dnd41	blood
24	chr2:178531000-178531400	Enhancers	GM12878-XiMat	blood
25	chr2:178531000-178531400	Flanking Active TSS	K562	blood
26	chr2:178531200-178531600	Enhancers	Muscle Satellite Cultured Cells	--
27	chr2:178531200-178532200	Weak transcription	HSMM	muscle
28	chr2:178531400-178534800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
29	chr2:178531400-178535800	Weak transcription	GM12878-XiMat	blood
30	chr2:178531400-178540000	Weak transcription	K562	blood
31	chr2:178531600-178533800	Weak transcription	Dnd41	blood
32	chr2:178531800-178535000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
33	chr2:178532200-178532800	Enhancers	HSMM	muscle
34	chr2:178532600-178532800	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
35	chr2:178532600-178532800	Enhancers	Psoas Muscle	Psoas
36	chr2:178532800-178534800	Weak transcription	Psoas Muscle	Psoas
37	chr2:178532800-178537000	Enhancers	Fetal Kidney	kidney
38	chr2:178532800-178538000	Weak transcription	HSMM	muscle
39	chr2:178533400-178535800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
40	chr2:178533800-178536600	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
41	chr2:178533800-178536600	Enhancers	Dnd41	blood
42	chr2:178534000-178537200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
43	chr2:178534200-178534800	Enhancers	Skeletal Muscle Female	skeletal muscle
44	chr2:178534200-178535400	Enhancers	Liver	Liver
45	chr2:178534200-178537000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
46	chr2:178534400-178537400	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
47	chr2:178534800-178535000	Enhancers	Right Atrium	heart
48	chr2:178534800-178535000	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
49	chr2:178534800-178536000	Enhancers	Psoas Muscle	Psoas
50	chr2:178534800-178536200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived

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