Variant report

Variant	nsv828561
Chromosome Location	chr19:43859394-43883620
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:139)
CpG islands
(count:61)
Chromatin interactive
region (count:1)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:139 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CEBPB	chr19:43876631-43876918	IMR90	lung:	n/a	n/a
2	CTCF	chr19:43873626-43873673	GM13976	blood:	n/a	n/a
3	CTCF	chr19:43881063-43881067	GM19239	blood:	n/a	n/a
4	CTCF	chr19:43881069-43881079	GM19239	blood:	n/a	n/a
5	CTCF	chr19:43881962-43882017	H1-hESC	embryonic stem cell:	n/a	n/a
6	CTCF	chr19:43862280-43862352	GM13976	blood:	n/a	n/a
7	CTCF	chr19:43861858-43861907	GM12891	blood:	n/a	n/a
8	CTCF	chr19:43880679-43880775	GM19239	blood:	n/a	n/a
9	CTCF	chr19:43861798-43861865	Lung_OC	lung:	n/a	n/a
10	CTCF	chr19:43881617-43881700	GM13976	blood:	n/a	n/a
11	CTCF	chr19:43862714-43862810	H1-hESC	embryonic stem cell:	n/a	n/a
12	CTCF	chr19:43870880-43871030	GM12864	blood:	n/a	n/a
13	CTCF	chr19:43881250-43881292	GM13977	blood:	n/a	n/a
14	CTCF	chr19:43873836-43873905	Lung_OC	lung:	n/a	n/a
15	CTCF	chr19:43869980-43870130	GM12872	blood:	n/a	n/a
16	CTCF	chr19:43881091-43881135	GM19239	blood:	n/a	n/a
17	CTCF	chr19:43861644-43861682	H1-hESC	embryonic stem cell:	n/a	n/a
18	CTCF	chr19:43861032-43861154	NHEK	skin:	n/a	n/a
19	CTCF	chr19:43861940-43861968	GM10266	blood:	n/a	n/a
20	CTCF	chr19:43861872-43861986	GM19239	blood:	n/a	n/a
21	CTCF	chr19:43860783-43860835	H1-hESC	embryonic stem cell:	n/a	n/a
22	CTCF	chr19:43880875-43880946	NHEK	skin:	n/a	n/a
23	CTCF	chr19:43862100-43862381	GM19239	blood:	n/a	n/a
24	CTCF	chr19:43881857-43882043	NHEK	skin:	n/a	n/a
25	CTCF	chr19:43874507-43874521	GM10248	blood:	n/a	n/a
26	CTCF	chr19:43863891-43863931	GM12892	blood:	n/a	n/a
27	CTCF	chr19:43867656-43867778	Hela-S3	cervix:	n/a	n/a
28	CTCF	chr19:43882271-43882340	Spleen_OC	spleen:	n/a	n/a
29	CTCF	chr19:43869472-43869521	H1-hESC	embryonic stem cell:	n/a	n/a
30	CTCF	chr19:43879059-43879112	Lung_OC	lung:	n/a	n/a
31	EP300	chr19:43876572-43877029	SK-N-SH_RA	brain:	n/a	n/a
32	EP300	chr19:43871367-43871775	SK-N-SH_RA	brain:	n/a	n/a
33	EP300	chr19:43871448-43871766	SK-N-SH_RA	brain:	n/a	n/a
34	EP300	chr19:43866140-43866781	SK-N-SH_RA	brain:	n/a	n/a
35	EP300	chr19:43876648-43877112	SK-N-SH_RA	brain:	n/a	n/a
36	EP300	chr19:43866199-43866840	SK-N-SH_RA	brain:	n/a	n/a
37	FOS	chr19:43876630-43876899	MCF10A-Er-Src	breast:	n/a	n/a
38	FOS	chr19:43876616-43876955	MCF10A-Er-Src	breast:	n/a	n/a
39	FOS	chr19:43869885-43870125	MCF10A-Er-Src	breast:	n/a	n/a
40	FOS	chr19:43872859-43873267	MCF10A-Er-Src	breast:	n/a	n/a
41	FOS	chr19:43869885-43870149	MCF10A-Er-Src	breast:	n/a	n/a
42	FOS	chr19:43866466-43866686	MCF10A-Er-Src	breast:	n/a	n/a
43	FOS	chr19:43872876-43873313	MCF10A-Er-Src	breast:	n/a	n/a
44	FOS	chr19:43876636-43876942	MCF10A-Er-Src	breast:	n/a	n/a
45	FOS	chr19:43866407-43866720	MCF10A-Er-Src	breast:	n/a	n/a
46	FOS	chr19:43872851-43873131	MCF10A-Er-Src	breast:	n/a	n/a
47	FOS	chr19:43869885-43870152	MCF10A-Er-Src	breast:	n/a	n/a
48	FOS	chr19:43869932-43870061	MCF10A-Er-Src	breast:	n/a	n/a
49	FOS	chr19:43866524-43866680	MCF10A-Er-Src	breast:	n/a	n/a
50	FOS	chr19:43876616-43876965	MCF10A-Er-Src	breast:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:43866487-43866537	PANC-1	pancreas:	n/a
2	chr19:43866487-43866537	SK-N-MC	brain:	n/a
3	chr19:43866487-43866537	AG09309	skin:	n/a
4	chr19:43866487-43866537	HCPEpiC	choroid plexus:	n/a
5	chr19:43866487-43866537	MCF-7	breast:	n/a
6	chr19:43866487-43866537	AoSMC	blood vessel:	n/a
7	chr19:43866487-43866537	Hela-S3	cervix:	n/a
8	chr19:43866487-43866537	HRPEpiC	eye:	n/a
9	chr19:43866487-43866537	GM12892	blood:	n/a
10	chr19:43866487-43866537	GM12878	blood:	n/a
11	chr19:43866487-43866537	HRCEpiC	kidney:	n/a
12	chr19:43866487-43866537	HepG2	liver:	n/a
13	chr19:43866487-43866537	HPAEpiC	pulmonary alveolar:	n/a
14	chr19:43866487-43866537	HAEpiC	amniotic membrane:	n/a
15	chr19:43866487-43866537	HMEC	breast:	n/a
16	chr19:43866487-43866537	ovcar-3	ovarian:	n/a
17	chr19:43866487-43866537	IMR90	lung:	fetal
18	chr19:43866487-43866537	ECC-1	luminal epithelium:	n/a
19	chr19:43866487-43866537	HCM	heart:	n/a
20	chr19:43866487-43866537	SAEC	small airway:	n/a
21	chr19:43866487-43866537	Jurkat	blood:	n/a
22	chr19:43866487-43866537	HNPCEpiC	eye:	n/a
23	chr19:43866487-43866537	HEK293	kidney:	embryo
24	chr19:43866487-43866537	HRE	kidney:	n/a
25	chr19:43866487-43866537	HCT-116	colon:	n/a
26	chr19:43866487-43866537	HCF	heart:	n/a
27	chr19:43866487-43866537	NH-A	brain:	n/a
28	chr19:43866487-43866537	RPTEC	kidney:	n/a
29	chr19:43866487-43866537	NB4	blood:	n/a
30	chr19:43866487-43866537	AG09319	gingival:	n/a
31	chr19:43866487-43866537	GM06990	blood:	n/a
32	chr19:43866487-43866537	PFSK-1	brain:	n/a
33	chr19:43866487-43866537	HIPEpiC	eye:	n/a
34	chr19:43866487-43866537	ProgFib	skin:	n/a
35	chr19:43866487-43866537	AG10803	skin:	n/a
36	chr19:43866487-43866537	LNCaP	prostate:	n/a
37	chr19:43866487-43866537	HL-60	blood:	n/a
38	chr19:43866487-43866537	Caco-2	colon:	n/a
39	chr19:43866487-43866537	BJ	skin:	n/a
40	chr19:43866487-43866537	GM19239	blood:	n/a
41	chr19:43866487-43866537	T-47D	breast:	n/a
42	chr19:43866487-43866537	BE2_C	brain:	n/a
43	chr19:43866487-43866537	Hepatocyte	liver:	n/a
44	chr19:43866487-43866537	A549	lung:	n/a
45	chr19:43866487-43866537	GM12891	blood:	n/a
46	chr19:43866487-43866537	AG04449	skin:	fetal
47	chr19:43866487-43866537	NHDF-neo	bronchial:	n/a
48	chr19:43866487-43866537	SK-N-SH	brain:	n/a
49	chr19:43866487-43866537	U87	brain:	n/a
50	chr19:43866487-43866537	CMK	blood:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr19:43857729..43859549-chr19:43967499..43969532,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AC005392.1-1	chr19:43864837-43864995	ENSG00000272396.1
2	lnc-AC005392.1-1	chr19:43866622-43866779	ENSG00000272396.1
3	lnc-AC005392.1-1	chr19:43872546-43872658	NONHSAT066597
4	lnc-AC005392.1-1	chr19:43872981-43873227	NONHSAT066597
5	lnc-AC005392.1-1	chr19:43872981-43873122	ENSG00000272396.1

No data

Variant related genes	Relation type
CD177P1	TF binding region
ENSG00000272396	TF binding region
CD177P1	CpG island
ENSG00000272396	CpG island
ENSG00000124466	chromatin interactions

Extended variants
information (count: 963 )
Associated
traits (count: 66 )

Variant overlapped rSNPs/rCNVs (count:963 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs578250430	chr19:43859414-43859415	Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs540898196	chr19:43859415-43859416	Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs554420017	chr19:43859422-43859423	Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs574315501	chr19:43859423-43859424	Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs182049506	chr19:43859426-43859427	Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs561870680	chr19:43859457-43859458	Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs1962260	chr19:43859549-43859550	Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs544205949	chr19:43859571-43859572	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs145873476	chr19:43859584-43859585	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs533079906	chr19:43859591-43859592	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs546455700	chr19:43859619-43859620	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs138701340	chr19:43859627-43859628	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs116634255	chr19:43859634-43859635	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs187659745	chr19:43859663-43859664	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs142707564	chr19:43859722-43859723	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs189077526	chr19:43859745-43859746	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs558151704	chr19:43859770-43859771	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs181035673	chr19:43859775-43859776	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs571631295	chr19:43859784-43859785	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs375328813	chr19:43859785-43859786	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs369543421	chr19:43859788-43859789	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs62113736	chr19:43859807-43859808	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs138962093	chr19:43859812-43859813	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs149427590	chr19:43859817-43859818	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs144809107	chr19:43859844-43859845	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs370248027	chr19:43859848-43859849	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs556441386	chr19:43859862-43859863	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs374615051	chr19:43859951-43859952	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs367981894	chr19:43859955-43859956	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs185339514	chr19:43859962-43859963	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs190200494	chr19:43859964-43859965	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs374285742	chr19:43859987-43859988	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs563207389	chr19:43859991-43859992	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs560964645	chr19:43859997-43859998	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs112666621	chr19:43860001-43860002	Bivalent Enhancer Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs73039860	chr19:43860030-43860031	Bivalent Enhancer Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs2286403	chr19:43860048-43860049	Bivalent Enhancer Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs71350665	chr19:43860053-43860054	Bivalent Enhancer Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs182730265	chr19:43860074-43860075	Bivalent Enhancer Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs71350666	chr19:43860076-43860077	Bivalent Enhancer Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs529134765	chr19:43860127-43860128	Bivalent Enhancer Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs111926611	chr19:43860138-43860139	Bivalent Enhancer Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs549163751	chr19:43860141-43860142	Bivalent Enhancer Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs562514247	chr19:43860187-43860188	Bivalent Enhancer Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs71337594	chr19:43860192-43860193	Bivalent Enhancer Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs551935907	chr19:43860204-43860205	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs571745049	chr19:43860207-43860208	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs368350368	chr19:43860249-43860250	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs199668750	chr19:43860251-43860252	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs200662237	chr19:43860255-43860256	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:66)

Disease	PMID	Source
Myelodysplastic syndrome	17634407	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	21637783	CNVD
Retinoblastoma	21504564	CNVD
Medulloblastoma	21979893	CNVD
Ovarian cancer	21720365	CNVD
Cancer	20164919	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Prostate cancer	18632612	CNVD
Autism	22495311	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Ductal carcinoma	22052326	CNVD
Congenital nephrotic syndrome	18421352	CNVD
Astrocytoma	17934521	CNVD
Leukemia	17361228	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Breast cancer	21858162	CNVD
Breast cancer	17603634	CNVD
Glioma	21971842	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Endometrial cancer	22040021	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Oligodendroglial tumors	17285580	CNVD
renal disease	20603712	CNVD
Salivary gland adenoid cystic carcinoma	17545515	CNVD
Breast cancer	16608533	CNVD
Neuroblastoma	18923191	CNVD
Breast cancer	21364760	CNVD
Chordoma	18071362	CNVD
Urothelial carcinoma	21177765	CNVD
small cell lung cancer	20016488	CNVD
Wilms tumour	21544195	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Metanephric adenoma	20802469	CNVD
Acute myeloid leukemia	16864856	CNVD
Bladder cancer	21909424	CNVD
Medulloblastoma	16783165	CNVD
Acute myeloid leukemia	20729466	CNVD
Lung cancer	18438408	CNVD
Astrocytoma	22246337	CNVD
Ovarian cancer	22174824	CNVD
Breast cancer	21509527	CNVD
Cancer	20164920	CNVD
Multiple myeloma	16616336	CNVD
Ovarian cancer	20800559	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	16272173	CNVD
Spondylocostal dysostosis	21085971	CNVD
Nicotine metabolism	21956041	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Glioblastoma multiforme	17002787	CNVD
Ovarian cancer	20844748	CNVD
Breast cancer	17133270	CNVD
Hepatocellular carcinoma	16750200	CNVD
Colorectal cancer	20459617	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Ovarian cancer	21240255	CNVD
Lung squamous cell carcinoma	22363434	CNVD

Chromatin state (count:115 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:43855800-43864200	Weak transcription	Right Atrium	heart
2	chr19:43858800-43859400	Active TSS	Rectal Mucosa Donor 29	rectum
3	chr19:43859000-43859400	Enhancers	Primary neutrophils fromperipheralblood	blood
4	chr19:43859000-43860000	Enhancers	Rectal Mucosa Donor 31	rectum
5	chr19:43859000-43864200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
6	chr19:43859400-43859600	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
7	chr19:43859400-43860200	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
8	chr19:43859600-43859800	Enhancers	Rectal Mucosa Donor 29	rectum
9	chr19:43859800-43860000	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
10	chr19:43859800-43860200	Enhancers	HMEC	breast
11	chr19:43860000-43860200	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
12	chr19:43860000-43864200	Weak transcription	Rectal Mucosa Donor 29	rectum
13	chr19:43860000-43864200	Weak transcription	Rectal Mucosa Donor 31	rectum
14	chr19:43860200-43864000	Weak transcription	Primary neutrophils fromperipheralblood	blood
15	chr19:43862800-43873200	Weak transcription	Gastric	stomach
16	chr19:43863000-43864200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr19:43864000-43864600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
18	chr19:43864000-43864600	Genic enhancers	Primary neutrophils fromperipheralblood	blood
19	chr19:43864200-43864600	Bivalent Enhancer	H9 Cell Line	embryonic stem cell
20	chr19:43864200-43864600	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
21	chr19:43864200-43864600	Enhancers	iPS-15b Cell Line	embryonic stem cell
22	chr19:43864200-43864600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
23	chr19:43864200-43864600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
24	chr19:43864200-43864600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
25	chr19:43864200-43864600	ZNF genes & repeats	Rectal Mucosa Donor 29	rectum
26	chr19:43864200-43864600	Enhancers	Rectal Mucosa Donor 31	rectum
27	chr19:43864200-43864600	ZNF genes & repeats	Right Atrium	heart
28	chr19:43864600-43866200	Weak transcription	Rectal Mucosa Donor 31	rectum
29	chr19:43864600-43866400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
30	chr19:43864600-43866400	Weak transcription	Rectal Mucosa Donor 29	rectum
31	chr19:43864600-43867600	Strong transcription	Primary neutrophils fromperipheralblood	blood
32	chr19:43864600-43868000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
33	chr19:43864600-43868200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
34	chr19:43866000-43866400	ZNF genes & repeats	Spleen	Spleen
35	chr19:43866000-43867000	Bivalent Enhancer	Fetal Stomach	stomach
36	chr19:43866200-43866400	Bivalent Enhancer	Fetal Muscle Trunk	muscle
37	chr19:43866200-43867000	Bivalent Enhancer	IMR90 fetal lung fibroblasts Cell Line	lung
38	chr19:43866200-43867000	Enhancers	Colonic Mucosa	Colon
39	chr19:43866200-43867000	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
40	chr19:43866200-43867000	Enhancers	Osteobl	bone
41	chr19:43866200-43867200	Enhancers	NHLF	lung
42	chr19:43866200-43867400	Enhancers	Rectal Mucosa Donor 31	rectum
43	chr19:43866400-43866600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
44	chr19:43866400-43866800	Bivalent Enhancer	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
45	chr19:43866400-43866800	Enhancers	Sigmoid Colon	Sigmoid Colon
46	chr19:43866400-43867000	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
47	chr19:43866400-43867200	Enhancers	Rectal Mucosa Donor 29	rectum
48	chr19:43866400-43868200	Weak transcription	Spleen	Spleen
49	chr19:43866600-43868000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
50	chr19:43866800-43868000	Weak transcription	Sigmoid Colon	Sigmoid Colon

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