Variant report

Variant	esv2762967
Chromosome Location	chr2:178546919-178577002
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:329)
CpG islands
(count:61)
Chromatin interactive
region (count:31)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:329 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:178556633-178557685	HepG2	liver:	n/a	n/a
2	ARID3A	chr2:178548061-178548261	K562	blood:	n/a	n/a
3	ARID3A	chr2:178547733-178547776	K562	blood:	n/a	n/a
4	ARID3A	chr2:178547107-178547190	K562	blood:	n/a	n/a
5	ARID3A	chr2:178557491-178557668	K562	blood:	n/a	n/a
6	ARID3A	chr2:178558288-178559366	K562	blood:	n/a	n/a
7	ARID3A	chr2:178554400-178554623	K562	blood:	n/a	n/a
8	ATF1	chr2:178554407-178554764	K562	blood:	n/a	n/a
9	ATF1	chr2:178558560-178559091	K562	blood:	n/a	n/a
10	ATF3	chr2:178558359-178559087	K562	blood:	n/a	n/a
11	BHLHE40	chr2:178547831-178548018	K562	blood:	n/a	n/a
12	BHLHE40	chr2:178558039-178559104	K562	blood:	n/a	n/a
13	BHLHE40	chr2:178557739-178557741	K562	blood:	n/a	n/a
14	BHLHE40	chr2:178554454-178554631	K562	blood:	n/a	n/a
15	BHLHE40	chr2:178548418-178548511	K562	blood:	n/a	n/a
16	CCNT2	chr2:178558442-178559135	K562	blood:	n/a	chr2:178558864-178558884
17	CCNT2	chr2:178554360-178554689	K562	blood:	n/a	n/a
18	CCNT2	chr2:178547689-178547927	K562	blood:	n/a	n/a
19	CEBPB	chr2:178569543-178569609	HepG2	liver:	n/a	chr2:178569565-178569576
20	CEBPB	chr2:178550933-178551169	HepG2	liver:	n/a	chr2:178551070-178551081
21	CEBPB	chr2:178549634-178549761	K562	blood:	n/a	chr2:178549681-178549692
22	CEBPB	chr2:178558429-178558729	A549	lung:	n/a	chr2:178558576-178558587
23	CEBPB	chr2:178550913-178551154	K562	blood:	n/a	chr2:178551070-178551081
24	CEBPB	chr2:178557271-178557521	Hela-S3	cervix:	n/a	n/a
25	CEBPB	chr2:178558425-178559027	K562	blood:	n/a	chr2:178558576-178558587
26	CEBPB	chr2:178558569-178558614	H1-hESC	embryonic stem cell:	n/a	chr2:178558576-178558587
27	CEBPB	chr2:178557191-178557717	A549	lung:	n/a	chr2:178557583-178557595
28	CEBPB	chr2:178558315-178559143	K562	blood:	n/a	chr2:178558576-178558587
29	CEBPB	chr2:178557275-178557602	A549	lung:	n/a	chr2:178557583-178557595
30	CEBPB	chr2:178551012-178551128	IMR90	lung:	n/a	chr2:178551070-178551081
31	CEBPB	chr2:178557240-178557599	HepG2	liver:	n/a	chr2:178557583-178557595
32	CEBPB	chr2:178558416-178558685	IMR90	lung:	n/a	chr2:178558576-178558587
33	CEBPB	chr2:178558399-178559087	K562	blood:	n/a	chr2:178558576-178558587
34	CEBPB	chr2:178550933-178551144	A549	lung:	n/a	chr2:178551070-178551081
35	CEBPB	chr2:178557263-178557501	HepG2	liver:	n/a	n/a
36	CEBPB	chr2:178550983-178551107	H1-hESC	embryonic stem cell:	n/a	chr2:178551070-178551081
37	CEBPB	chr2:178549557-178549765	HepG2	liver:	n/a	chr2:178549681-178549692
38	CEBPB	chr2:178558415-178558716	HepG2	liver:	n/a	chr2:178558576-178558587
39	CEBPD	chr2:178558362-178559103	K562	blood:	n/a	n/a
40	CEBPD	chr2:178558470-178559144	K562	blood:	n/a	n/a
41	CTCF	chr2:178557665-178557805	Gliobla	brain:	n/a	n/a
42	CTCF	chr2:178557680-178557830	AG09319	gingival:	n/a	n/a
43	CTCF	chr2:178557660-178557810	SAEC	small airway:	n/a	n/a
44	CTCF	chr2:178556000-178556150	A549	lung:	n/a	n/a
45	CTCF	chr2:178555980-178556130	HCT-116	colon:	n/a	chr2:178555992-178556001
46	CTCF	chr2:178557680-178557830	HRE	kidney:	n/a	n/a
47	CTCF	chr2:178557600-178557750	HCM	heart:	n/a	n/a
48	CTCF	chr2:178557600-178557750	HEK293	kidney:	n/a	n/a
49	CTCF	chr2:178556117-178556158	Hela-S3	cervix:	n/a	n/a
50	CTCF	chr2:178556040-178556190	GM12865	blood:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:178556488-178556538	BJ	skin:	n/a
2	chr2:178556488-178556538	GM19239	blood:	n/a
3	chr2:178556488-178556538	T-47D	breast:	n/a
4	chr2:178556488-178556538	SAEC	small airway:	n/a
5	chr2:178556488-178556538	HepG2	liver:	n/a
6	chr2:178556488-178556538	PANC-1	pancreas:	n/a
7	chr2:178556488-178556538	RPTEC	kidney:	n/a
8	chr2:178556488-178556538	IMR90	lung:	fetal
9	chr2:178556488-178556538	CMK	blood:	n/a
10	chr2:178556488-178556538	A549	lung:	n/a
11	chr2:178556488-178556538	HL-60	blood:	n/a
12	chr2:178556488-178556538	ProgFib	skin:	n/a
13	chr2:178556488-178556538	H1-hESC	embryonic stem cell:	embryo
14	chr2:178556488-178556538	LNCaP	prostate:	n/a
15	chr2:178556488-178556538	Caco-2	colon:	n/a
16	chr2:178556488-178556538	Jurkat	blood:	n/a
17	chr2:178556488-178556538	GM12891	blood:	n/a
18	chr2:178556488-178556538	NHDF-neo	bronchial:	n/a
19	chr2:178556488-178556538	NB4	blood:	n/a
20	chr2:178556488-178556538	SKMC	muscle:	n/a
21	chr2:178556488-178556538	AG04449	skin:	fetal
22	chr2:178556488-178556538	HIPEpiC	eye:	n/a
23	chr2:178556488-178556538	HRCEpiC	kidney:	n/a
24	chr2:178556488-178556538	NT2-D1	testis:	n/a
25	chr2:178556488-178556538	GM06990	blood:	n/a
26	chr2:178556488-178556538	HCPEpiC	choroid plexus:	n/a
27	chr2:178556488-178556538	HPAEpiC	pulmonary alveolar:	n/a
28	chr2:178556488-178556538	HCF	heart:	n/a
29	chr2:178556488-178556538	ECC-1	luminal epithelium:	n/a
30	chr2:178556488-178556538	HEEpiC	esophagus:	n/a
31	chr2:178556488-178556538	HCM	heart:	n/a
32	chr2:178556488-178556538	AG09319	gingival:	n/a
33	chr2:178556488-178556538	AG04450	lung:	fetal
34	chr2:178556488-178556538	K562	blood:	n/a
35	chr2:178556488-178556538	HMEC	breast:	n/a
36	chr2:178556488-178556538	HRPEpiC	eye:	n/a
37	chr2:178556488-178556538	SK-N-SH	brain:	n/a
38	chr2:178556488-178556538	U87	brain:	n/a
39	chr2:178556488-178556538	HCT-116	colon:	n/a
40	chr2:178556488-178556538	HUVEC	blood vessel:	n/a
41	chr2:178556488-178556538	BE2_C	brain:	n/a
42	chr2:178556488-178556538	MCF-7	breast:	n/a
43	chr2:178556488-178556538	Hela-S3	cervix:	n/a
44	chr2:178556488-178556538	HAEpiC	amniotic membrane:	n/a
45	chr2:178556488-178556538	GM12878	blood:	n/a
46	chr2:178556488-178556538	AG10803	skin:	n/a
47	chr2:178556488-178556538	NH-A	brain:	n/a
48	chr2:178556488-178556538	HNPCEpiC	eye:	n/a
49	chr2:178556488-178556538	SK-N-SH_RA	brain:	n/a
50	chr2:178556488-178556538	PrEC	prostate:	n/a

(count:31 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:178553724..178556122-chr2:178557669..178561053,4	K562	blood:
2	chr2:178563706..178566606-chr2:178575234..178578088,2	K562	blood:
3	chr2:178553724..178556122-chr2:178557669..178561053,4	K562	blood:
4	chr2:178570926..178572812-chr2:178573756..178576490,2	K562	blood:
5	chr2:178557827..178560384-chr2:178566181..178567818,2	K562	blood:
6	chr2:178554622..178556769-chr2:178559553..178561777,2	K562	blood:
7	chr2:178554622..178556769-chr2:178559553..178561777,2	K562	blood:
8	chr2:178561207..178563093-chr2:178570078..178571660,2	MCF-7	breast:
9	chr2:178567581..178570235-chr2:178573899..178577717,4	K562	blood:
10	chr2:178570926..178572812-chr2:178573756..178576490,2	K562	blood:
11	chr2:178563706..178566606-chr2:178575234..178578088,2	K562	blood:
12	chr2:178562301..178565158-chr2:178568749..178571184,2	K562	blood:
13	chr2:178559293..178562880-chr2:178620510..178622541,4	K562	blood:
14	chr2:178561612..178563811-chr2:178565917..178568583,4	K562	blood:
15	chr2:178556581..178559111-chr2:178571009..178573713,2	K562	blood:
16	chr2:178557827..178560384-chr2:178566181..178567818,2	K562	blood:
17	chr2:178560703..178563309-chr2:178574867..178577003,2	K562	blood:
18	chr2:178561119..178564111-chr2:178566483..178568629,4	K562	blood:
19	chr2:178416053..178418708-chr2:178570239..178572777,3	MCF-7	breast:
20	chr2:178257363..178259725-chr2:178564767..178567324,2	K562	blood:
21	chr2:178546208..178548509-chr2:178552748..178555951,3	K562	blood:
22	chr2:178568725..178571101-chr2:178581270..178584257,2	K562	blood:
23	chr2:178567581..178570235-chr2:178573899..178577717,4	K562	blood:
24	chr2:178562301..178564741-chr2:178568694..178570249,2	K562	blood:
25	chr2:178540518..178542600-chr2:178544661..178547619,2	MCF-7	breast:
26	chr2:178573812..178575590-chr2:178578150..178581099,2	K562	blood:
27	chr2:178557613..178559704-chr2:178561778..178563487,2	K562	blood:
28	chr2:178454525..178456445-chr2:178573217..178575511,2	K562	blood:
29	chr2:178561207..178563093-chr2:178570078..178571660,2	MCF-7	breast:
30	chr2:178536377..178538004-chr2:178556463..178558808,2	K562	blood:
31	chr2:178556581..178559111-chr2:178571009..178573713,2	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	chr2:178563157-178563299	ENSG00000229941.1
3	lnc-AGPS-3	chr2:178567216-178567477	ENSG00000229941.1
4	lnc-AGPS-3	chr2:178565822-178565956	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
ENSG00000018510	chromatin interactions
ENSG00000116044	chromatin interactions
ENSG00000229941	chromatin interactions
ENSG00000128655	chromatin interactions
ENSG00000213963	chromatin interactions
ENSG00000196659	chromatin interactions

Extended variants
information (count: 1156 )
Associated
traits (count: 50 )

Variant overlapped rSNPs/rCNVs (count:1156 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs75667657	chr2:178546986-178546987	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs551268509	chr2:178546987-178546988	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs569519891	chr2:178546988-178546989	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs550842982	chr2:178547020-178547021	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs189157732	chr2:178547025-178547026	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs565819920	chr2:178547027-178547028	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs569258263	chr2:178547035-178547036	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs534808400	chr2:178547038-178547039	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs551630378	chr2:178547077-178547078	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs181883643	chr2:178547078-178547079	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs116401527	chr2:178547085-178547086	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs112409669	chr2:178547107-178547108	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs537165906	chr2:178547122-178547123	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs573905976	chr2:178547170-178547171	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs536258627	chr2:178547195-178547196	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs114929728	chr2:178547202-178547203	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs573050365	chr2:178547205-178547206	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs545177401	chr2:178547231-178547232	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs185847356	chr2:178547232-178547233	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs78758513	chr2:178547239-178547240	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs539805792	chr2:178547240-178547241	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs561633591	chr2:178547264-178547265	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs528885393	chr2:178547376-178547377	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs553430954	chr2:178547398-178547399	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs573926133	chr2:178547399-178547400	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs573477520	chr2:178547455-178547456	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs57733755	chr2:178547462-178547463	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs397956878	chr2:178547463-178547464	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs368287153	chr2:178547464-178547465	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs150331573	chr2:178547519-178547520	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs528774312	chr2:178547622-178547623	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs77223227	chr2:178547639-178547640	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs551516292	chr2:178547692-178547693	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs556676634	chr2:178547695-178547696	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs571326218	chr2:178547702-178547703	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs73979519	chr2:178547738-178547739	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs191745948	chr2:178547739-178547740	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs77389369	chr2:178547777-178547778	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs536245239	chr2:178547818-178547819	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs116248227	chr2:178547866-178547867	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs572914364	chr2:178547904-178547905	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs538716952	chr2:178547908-178547909	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs544408540	chr2:178547978-178547979	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs183203202	chr2:178547991-178547992	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs575706907	chr2:178547996-178547997	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs6433690	chr2:178548022-178548023	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs562602420	chr2:178548035-178548036	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs375345263	chr2:178548036-178548037	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs575237961	chr2:178548050-178548051	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs7562940	chr2:178548054-178548055	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	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:204 , 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	chr2:178544000-178548000	Enhancers	K562	blood
4	chr2:178544600-178552600	Weak transcription	Fetal Intestine Small	intestine
5	chr2:178545000-178547000	Enhancers	Duodenum Mucosa	Duodenum
6	chr2:178545200-178548000	Weak transcription	Adipose Nuclei	Adipose
7	chr2:178545400-178549200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
8	chr2:178545800-178547400	Enhancers	iPS-18 Cell Line	embryonic stem cell
9	chr2:178546000-178547200	Enhancers	HUES6 Cell Line	embryonic stem cell
10	chr2:178546200-178548600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
11	chr2:178546400-178547000	Enhancers	ES-I3 Cell Line	embryonic stem cell
12	chr2:178546400-178547200	Enhancers	H1 Cell Line	embryonic stem cell
13	chr2:178546400-178547200	Enhancers	H9 Cell Line	embryonic stem cell
14	chr2:178546400-178547200	Enhancers	HUES64 Cell Line	embryonic stem cell
15	chr2:178546400-178547200	Enhancers	iPS-15b Cell Line	embryonic stem cell
16	chr2:178546800-178547200	Enhancers	Small Intestine	intestine
17	chr2:178546800-178554400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
18	chr2:178547000-178552800	Weak transcription	Duodenum Mucosa	Duodenum
19	chr2:178547200-178548200	Enhancers	HepG2	liver
20	chr2:178547400-178549000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
21	chr2:178547400-178554400	Weak transcription	Fetal Kidney	kidney
22	chr2:178548000-178548600	Enhancers	Adipose Nuclei	Adipose
23	chr2:178548000-178548600	Flanking Active TSS	K562	blood
24	chr2:178548200-178549400	Weak transcription	HepG2	liver
25	chr2:178548600-178549200	Weak transcription	Adipose Nuclei	Adipose
26	chr2:178548600-178549400	Enhancers	K562	blood
27	chr2:178548600-178549600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
28	chr2:178549200-178549400	Enhancers	Adipose Nuclei	Adipose
29	chr2:178549200-178550000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
30	chr2:178549400-178550000	Enhancers	Stomach Mucosa	stomach
31	chr2:178549400-178550200	Enhancers	HepG2	liver
32	chr2:178549400-178554400	Weak transcription	K562	blood
33	chr2:178549600-178550400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
34	chr2:178550000-178554200	Weak transcription	Stomach Mucosa	stomach
35	chr2:178550000-178557000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
36	chr2:178550400-178555800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
37	chr2:178552600-178552800	Enhancers	Sigmoid Colon	Sigmoid Colon
38	chr2:178552600-178553000	Enhancers	Fetal Intestine Small	intestine
39	chr2:178552800-178553000	Enhancers	Fetal Intestine Large	intestine
40	chr2:178552800-178553000	Bivalent Enhancer	Sigmoid Colon	Sigmoid Colon
41	chr2:178552800-178553200	Enhancers	Duodenum Mucosa	Duodenum
42	chr2:178552800-178553200	Enhancers	Rectal Mucosa Donor 31	rectum
43	chr2:178552800-178554000	Enhancers	Dnd41	blood
44	chr2:178553000-178553400	Enhancers	Rectal Mucosa Donor 29	rectum
45	chr2:178553000-178554200	Weak transcription	Fetal Intestine Small	intestine
46	chr2:178553000-178557000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
47	chr2:178553000-178557000	Weak transcription	Fetal Intestine Large	intestine
48	chr2:178553200-178557000	Weak transcription	Rectal Mucosa Donor 31	rectum
49	chr2:178553200-178557200	Weak transcription	Duodenum Mucosa	Duodenum
50	chr2:178553400-178554400	Weak transcription	Rectal Mucosa Donor 29	rectum

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