Variant report

Variant	esv1794782
Chromosome Location	chr1:174900761-174925112
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:283)
CpG islands
(count:61)
Chromatin interactive
region (count:14)
LncRNA
region (count:8)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:283 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:174911756-174912274	HepG2	liver:	n/a	n/a
2	ARID3A	chr1:174922941-174923504	HepG2	liver:	n/a	n/a
3	ATF2	chr1:174922398-174923498	GM12878	blood:	n/a	n/a
4	ATF2	chr1:174922323-174923218	GM12878	blood:	n/a	n/a
5	BATF	chr1:174907522-174907768	GM12878	blood:	n/a	n/a
6	BATF	chr1:174922759-174923152	GM12878	blood:	n/a	n/a
7	BATF	chr1:174922361-174922707	GM12878	blood:	n/a	n/a
8	BATF	chr1:174907521-174907734	GM12878	blood:	n/a	n/a
9	BCL11A	chr1:174922772-174923145	GM12878	blood:	n/a	n/a
10	BCL11A	chr1:174922688-174923186	GM12878	blood:	n/a	n/a
11	BHLHE40	chr1:174911712-174911718	HepG2	liver:	n/a	n/a
12	BHLHE40	chr1:174922181-174923459	GM12878	blood:	n/a	n/a
13	BRCA1	chr1:174923841-174923868	Hela-S3	cervix:	n/a	n/a
14	CEBPB	chr1:174921570-174921696	HepG2	liver:	n/a	chr1:174921598-174921609
15	CEBPB	chr1:174911952-174912280	K562	blood:	n/a	n/a
16	CEBPB	chr1:174911955-174912270	A549	lung:	n/a	n/a
17	CEBPB	chr1:174922955-174923113	HepG2	liver:	n/a	n/a
18	CEBPB	chr1:174911966-174912272	IMR90	lung:	n/a	n/a
19	CEBPB	chr1:174911966-174912301	MCF-7	breast:	n/a	n/a
20	CEBPB	chr1:174911985-174912303	K562	blood:	n/a	n/a
21	CEBPB	chr1:174911963-174912383	HepG2	liver:	n/a	n/a
22	CEBPB	chr1:174911957-174912304	Hela-S3	cervix:	n/a	n/a
23	CEBPB	chr1:174922307-174923541	GM12878	blood:	n/a	n/a
24	CEBPB	chr1:174923438-174923445	H1-hESC	embryonic stem cell:	n/a	n/a
25	CEBPB	chr1:174911870-174912406	HepG2	liver:	n/a	n/a
26	CEBPB	chr1:174922738-174923205	HepG2	liver:	n/a	n/a
27	CEBPB	chr1:174921561-174921757	H1-hESC	embryonic stem cell:	n/a	chr1:174921598-174921609
28	CEBPB	chr1:174911853-174912403	MCF-7	breast:	n/a	n/a
29	CEBPB	chr1:174912024-174912260	HepG2	liver:	n/a	n/a
30	CEBPB	chr1:174922757-174923014	A549	lung:	n/a	n/a
31	CEBPB	chr1:174911848-174912330	HepG2	liver:	n/a	n/a
32	CEBPD	chr1:174911976-174912307	HepG2	liver:	n/a	n/a
33	CHD1	chr1:174922569-174923110	GM12878	blood:	n/a	n/a
34	CHD2	chr1:174922602-174923193	GM12878	blood:	n/a	n/a
35	CREB1	chr1:174922552-174923175	GM12878	blood:	n/a	n/a
36	CTCF	chr1:174901900-174902050	AoAF	blood vessel:	n/a	n/a
37	CTCF	chr1:174901921-174901997	MCF-7	breast:	n/a	n/a
38	CTCF	chr1:174902000-174902150	HFF-Myc	foreskin:	n/a	n/a
39	CTCF	chr1:174901820-174901970	HVMF	connective:	n/a	n/a
40	CTCF	chr1:174901840-174901990	AG10803	skin:	n/a	n/a
41	CTCF	chr1:174901920-174902070	NHDF-neo	bronchial:	n/a	n/a
42	CTCF	chr1:174901893-174901999	IMR90	lung:	n/a	n/a
43	CTCF	chr1:174901880-174902030	AG04449	skin:	n/a	n/a
44	CTCF	chr1:174901880-174902030	HCPEpiC	choroid plexus:	n/a	n/a
45	CTCF	chr1:174901900-174902050	GM12873	blood:	n/a	n/a
46	CTCF	chr1:174901893-174901986	Lung_OC	lung:	n/a	n/a
47	CTCF	chr1:174901880-174902030	HCT-116	colon:	n/a	n/a
48	CTCF	chr1:174901860-174902010	AG10803	skin:	n/a	n/a
49	CTCF	chr1:174901900-174902050	HAc	cerebellar:	n/a	n/a
50	CTCF	chr1:174902060-174902210	HEK293	kidney:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:174909464-174909514	HIPEpiC	eye:	n/a
2	chr1:174909464-174909514	SK-N-SH	brain:	n/a
3	chr1:174909464-174909514	AG04449	skin:	fetal
4	chr1:174909464-174909514	BJ	skin:	n/a
5	chr1:174909464-174909514	HUVEC	blood vessel:	n/a
6	chr1:174909464-174909514	GM12878	blood:	n/a
7	chr1:174909464-174909514	H1-hESC	embryonic stem cell:	embryo
8	chr1:174909464-174909514	HEK293	kidney:	embryo
9	chr1:174909464-174909514	IMR90	lung:	fetal
10	chr1:174909464-174909514	AG10803	skin:	n/a
11	chr1:174909464-174909514	SK-N-SH_RA	brain:	n/a
12	chr1:174909464-174909514	BE2_C	brain:	n/a
13	chr1:174909464-174909514	ECC-1	luminal epithelium:	n/a
14	chr1:174909464-174909514	GM12892	blood:	n/a
15	chr1:174909464-174909514	HL-60	blood:	n/a
16	chr1:174909464-174909514	NHBE	bronchial:	n/a
17	chr1:174909464-174909514	NT2-D1	testis:	n/a
18	chr1:174909464-174909514	MCF-7	breast:	n/a
19	chr1:174909464-174909514	PrEC	prostate:	n/a
20	chr1:174909464-174909514	AG04450	lung:	fetal
21	chr1:174909464-174909514	PFSK-1	brain:	n/a
22	chr1:174909464-174909514	HepG2	liver:	n/a
23	chr1:174909464-174909514	HCM	heart:	n/a
24	chr1:174909464-174909514	HCF	heart:	n/a
25	chr1:174909464-174909514	RPTEC	kidney:	n/a
26	chr1:174909464-174909514	GM06990	blood:	n/a
27	chr1:174909464-174909514	HRCEpiC	kidney:	n/a
28	chr1:174909464-174909514	GM19239	blood:	n/a
29	chr1:174909464-174909514	NH-A	brain:	n/a
30	chr1:174909464-174909514	U87	brain:	n/a
31	chr1:174909464-174909514	GM12891	blood:	n/a
32	chr1:174909464-174909514	HCT-116	colon:	n/a
33	chr1:174909464-174909514	SKMC	muscle:	n/a
34	chr1:174909464-174909514	SAEC	small airway:	n/a
35	chr1:174909464-174909514	SK-N-MC	brain:	n/a
36	chr1:174909464-174909514	NB4	blood:	n/a
37	chr1:174909464-174909514	HCPEpiC	choroid plexus:	n/a
38	chr1:174909464-174909514	ProgFib	skin:	n/a
39	chr1:174909464-174909514	Jurkat	blood:	n/a
40	chr1:174909464-174909514	K562	blood:	n/a
41	chr1:174909464-174909514	HRPEpiC	eye:	n/a
42	chr1:174909464-174909514	HNPCEpiC	eye:	n/a
43	chr1:174909464-174909514	AG09319	gingival:	n/a
44	chr1:174909464-174909514	Hela-S3	cervix:	n/a
45	chr1:174909464-174909514	HMEC	breast:	n/a
46	chr1:174909464-174909514	Hepatocyte	liver:	n/a
47	chr1:174909464-174909514	HRE	kidney:	n/a
48	chr1:174909464-174909514	LNCaP	prostate:	n/a
49	chr1:174909464-174909514	HAEpiC	amniotic membrane:	n/a
50	chr1:174909464-174909514	CMK	blood:	n/a

(count:14 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:174908320..174910168-chr1:174924231..174926585,2	K562	blood:
2	chr1:174899181..174902088-chr1:174902250..174905277,3	K562	blood:
3	chr1:174923198..174925384-chr1:174966768..174969238,3	K562	blood:
4	chr1:174923792..174926016-chr1:174927596..174930266,2	MCF-7	breast:
5	chr1:174896436..174898470-chr1:174907347..174910296,2	K562	blood:
6	chr1:174922181..174924698-chr1:174966768..174969386,2	K562	blood:
7	chr1:174908320..174910168-chr1:174924231..174926585,2	K562	blood:
8	chr1:174918226..174919884-chr1:174922413..174925557,3	MCF-7	breast:
9	chr1:174909477..174911004-chr1:174913375..174915350,2	MCF-7	breast:
10	chr1:174903721..174906103-chr1:174964849..174967396,3	K562	blood:
11	chr1:174918637..174921043-chr1:174923032..174925557,2	K562	blood:
12	chr1:174899181..174902088-chr1:174902250..174905277,3	K562	blood:
13	chr1:174909477..174911004-chr1:174913375..174915350,2	MCF-7	breast:
14	chr1:174889741..174892374-chr1:174899175..174902170,2	K562	blood:

(count:8 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MRPS14-2	chr1:174914660-174915031	ENSG00000229531.1
2	lnc-MRPS14-2	chr1:174904084-174904237	ENSG00000229531.1
3	lnc-MRPS14-2	chr1:174914961-174915031	ENSG00000229531.1
4	lnc-MRPS14-2	chr1:174904536-174904643	ENSG00000229531.1
5	lnc-MRPS14-2	chr1:174907584-174907661	ENSG00000229531.1
6	lnc-MRPS14-2	chr1:174917860-174918013	ENSG00000229531.1
7	lnc-MRPS14-2	chr1:174917860-174918013	ENSG00000229531.1
8	lnc-MRPS14-2	chr1:174923294-174923398	ENSG00000229531.1

No data

Variant related genes	Relation type
ENSG00000229531	TF binding region
ENSG00000229531	CpG island
ENSG00000235869	chromatin interactions
ENSG00000229531	chromatin interactions
ENSG00000116161	chromatin interactions
ENSG00000252552	chromatin interactions
HBP1	miRNA target sites
HDAC4	miRNA target sites

Extended variants
information (count: 819 )
Associated
traits (count: 91 )

Variant overlapped rSNPs/rCNVs (count:819 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4651231	chr1:174900761-174900762	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs190998161	chr1:174900843-174900844	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs553554286	chr1:174900916-174900917	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs147483762	chr1:174901014-174901015	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs184231947	chr1:174901017-174901018	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs140030923	chr1:174901055-174901056	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs551384421	chr1:174901125-174901126	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs77759378	chr1:174901126-174901127	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs369022922	chr1:174901127-174901128	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs78353863	chr1:174901128-174901129	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs532860564	chr1:174901149-174901150	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs12095395	chr1:174901152-174901153	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs80239267	chr1:174901165-174901166	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs188782902	chr1:174901221-174901222	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs151034054	chr1:174901248-174901249	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs533857750	chr1:174901277-174901278	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs193025571	chr1:174901300-174901301	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs573500472	chr1:174901402-174901403	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs536303621	chr1:174901403-174901404	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs12047680	chr1:174901407-174901408	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs12047710	chr1:174901410-174901411	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs12047713	chr1:174901419-174901420	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs12568184	chr1:174901430-174901431	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs545707005	chr1:174901439-174901440	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs571817085	chr1:174901512-174901513	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs556277183	chr1:174901561-174901562	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs183491323	chr1:174901596-174901597	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs370691422	chr1:174901605-174901606	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs576022351	chr1:174901627-174901628	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs562474615	chr1:174901633-174901634	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs565426330	chr1:174901645-174901646	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs572668244	chr1:174901683-174901684	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs575908523	chr1:174901710-174901711	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs541505443	chr1:174901712-174901713	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs67203477	chr1:174901780-174901781	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
36	rs188138314	chr1:174901781-174901782	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs143985247	chr1:174901872-174901873	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs33999051	chr1:174901874-174901875	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs527406349	chr1:174901878-174901879	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs191787062	chr1:174901893-174901894	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs112667452	chr1:174901902-174901903	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs144357129	chr1:174901906-174901907	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs560690797	chr1:174901932-174901933	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs183583013	chr1:174901985-174901986	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs571174760	chr1:174901992-174901993	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs542412959	chr1:174902099-174902100	Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs532720909	chr1:174902130-174902131	Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs374016386	chr1:174902158-174902159	Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs552790819	chr1:174902173-174902174	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs547384653	chr1:174902221-174902222	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:91)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Autism	22495311	CNVD
Hepatocellular carcinoma	16750200	CNVD
Liposarcoma	21253554	CNVD
Burkitt''s lymphoma	18698080	CNVD
Melanoma	18172304	CNVD
Cancer	21183584	CNVD
Multiple myeloma	16461302	CNVD
Rett syndrome	21593744	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Medulloblastoma	21979893	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
Non-small cell lung cancer	21829676	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Non-small cell lung cancer	21044232	CNVD
Cervical cancer	21063398	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	20632083	CNVD
Endometrial cancer	22040021	CNVD
Ewing''s sarcoma	21437220	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	21264507	CNVD
Multiple myeloma	21628407	CNVD
Cancer	16751803	CNVD
Prostate cancer	16705090	CNVD
Neuroblastoma	19435921	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16461572	CNVD
Intracranial tumor	16823260	CNVD
Medulloblastoma	18056178	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Neuroblastoma	21899760	CNVD
Bladder cancer	19088036	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17002787	CNVD
Breast cancer	21858162	CNVD
Retinoblastoma	19183342	CNVD
Non-small cell lung cancer	21385341	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Chordoma	18071362	CNVD
Hepatocellular carcinoma	18803288	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Urothelial carcinoma	21177765	CNVD
Burkitt''s lymphoma	19759907	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Testicular germ cell tumor	18059402	CNVD
Trisomy 5 syndrome	21098271	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Neuroblastoma	18923191	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ewing''s sarcoma	17952124	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Developmental delay	21147756	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Breast cancer	21509527	CNVD
Glioblastoma multiforme	17369134	CNVD
Cancer	17440070	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	21611746	CNVD
Myelofibrosis	22110671	CNVD
Autism	22241247	CNVD
Breast cancer	16397240	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:621 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:174861400-174902400	Weak transcription	Left Ventricle	heart
2	chr1:174874000-174910000	Weak transcription	H9 Cell Line	embryonic stem cell
3	chr1:174874200-174938200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr1:174876800-174933600	Weak transcription	Aorta	Aorta
5	chr1:174886000-174907200	Weak transcription	Primary T cells from cord blood	blood
6	chr1:174886400-174911600	Weak transcription	Sigmoid Colon	Sigmoid Colon
7	chr1:174889600-174907400	Weak transcription	Primary B cells from cord blood	blood
8	chr1:174891800-174908600	Weak transcription	HUES6 Cell Line	embryonic stem cell
9	chr1:174892200-174905000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
10	chr1:174893400-174907600	Weak transcription	GM12878-XiMat	blood
11	chr1:174897400-174903600	Weak transcription	Pancreas	Pancrea
12	chr1:174897400-174910000	Weak transcription	Gastric	stomach
13	chr1:174897800-174907200	Weak transcription	Duodenum Mucosa	Duodenum
14	chr1:174898800-174910600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
15	chr1:174899400-174900800	Genic enhancers	iPS-20b Cell Line	embryonic stem cell
16	chr1:174899600-174901000	Enhancers	Brain Inferior Temporal Lobe	brain
17	chr1:174899800-174915200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
18	chr1:174900000-174900800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr1:174900000-174900800	Enhancers	HUES48 Cell Line	embryonic stem cell
20	chr1:174900000-174900800	Enhancers	iPS-18 Cell Line	embryonic stem cell
21	chr1:174900000-174900800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
22	chr1:174900000-174901000	Enhancers	iPS-15b Cell Line	embryonic stem cell
23	chr1:174900000-174901600	Enhancers	Brain Hippocampus Middle	brain
24	chr1:174900000-174902200	Weak transcription	H1 Cell Line	embryonic stem cell
25	chr1:174900000-174902200	Enhancers	HUES64 Cell Line	embryonic stem cell
26	chr1:174900200-174901000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
27	chr1:174900200-174901000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
28	chr1:174900200-174901400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
29	chr1:174900200-174901400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
30	chr1:174900200-174901600	Enhancers	Cortex derived primary cultured neurospheres	brain
31	chr1:174900200-174901600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
32	chr1:174900400-174900800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
33	chr1:174900400-174900800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
34	chr1:174900400-174900800	Enhancers	Brain Angular Gyrus	brain
35	chr1:174900400-174900800	Enhancers	Brain Anterior Caudate	brain
36	chr1:174900400-174900800	Enhancers	Brain Cingulate Gyrus	brain
37	chr1:174900400-174901000	Enhancers	HMEC	breast
38	chr1:174900400-174901000	Enhancers	NHEK	skin
39	chr1:174900400-174901200	Enhancers	Fetal Intestine Small	intestine
40	chr1:174900400-174902600	Enhancers	Brain Substantia Nigra	brain
41	chr1:174900600-174900800	Enhancers	Rectal Mucosa Donor 29	rectum
42	chr1:174900600-174901000	Enhancers	ES-I3 Cell Line	embryonic stem cell
43	chr1:174900600-174901000	Enhancers	Pancreatic Islets	Pancreatic Islet
44	chr1:174900600-174901800	Enhancers	Fetal Intestine Large	intestine
45	chr1:174900800-174901400	Weak transcription	HUES48 Cell Line	embryonic stem cell
46	chr1:174900800-174901600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
47	chr1:174900800-174902000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
48	chr1:174900800-174902000	Weak transcription	Brain Anterior Caudate	brain
49	chr1:174900800-174902000	Weak transcription	Brain Cingulate Gyrus	brain
50	chr1:174900800-174904600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell

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