Variant report

Variant	esv3318546
Chromosome Location	chr19:41972494-42008328
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:216)
CpG islands
(count:61)
Chromatin interactive
region (count:5)
LncRNA
region (count:27)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:216 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr19:41985894-41986022	K562	blood:	n/a	n/a
2	ATF1	chr19:41985515-41985820	K562	blood:	n/a	n/a
3	ATF3	chr19:42007044-42007229	K562	blood:	n/a	n/a
4	BACH1	chr19:41985825-41985834	K562	blood:	n/a	n/a
5	BATF	chr19:42007315-42007464	GM12878	blood:	n/a	n/a
6	BHLHE40	chr19:42007430-42007554	K562	blood:	n/a	n/a
7	BHLHE40	chr19:41986254-41986585	K562	blood:	n/a	n/a
8	BHLHE40	chr19:41985631-41985823	K562	blood:	n/a	n/a
9	CBX3	chr19:41985547-41986099	K562	blood:	n/a	n/a
10	CBX3	chr19:42007176-42007860	HCT-116	colon:	n/a	n/a
11	CEBPB	chr19:41992986-41993092	IMR90	lung:	n/a	chr19:41993068-41993079
12	CEBPB	chr19:41992947-41993198	A549	lung:	n/a	chr19:41993068-41993079
13	CEBPB	chr19:41992260-41992553	A549	lung:	n/a	n/a
14	CEBPB	chr19:41992290-41992562	HepG2	liver:	n/a	n/a
15	CEBPB	chr19:41992919-41993068	HepG2	liver:	n/a	n/a
16	CEBPB	chr19:41992890-41993261	HepG2	liver:	n/a	chr19:41993068-41993079
17	CEBPB	chr19:41992465-41992478	H1-hESC	embryonic stem cell:	n/a	n/a
18	CTCF	chr19:41984380-41984530	GM06990	blood:	n/a	n/a
19	CTCF	chr19:41990980-41991130	A549	lung:	n/a	n/a
20	CTCF	chr19:41984420-41984570	A549	lung:	n/a	n/a
21	CTCF	chr19:41982900-41983050	GM12869	blood:	n/a	n/a
22	CTCF	chr19:41992387-41992397	Kidney_OC	kidney:	n/a	n/a
23	CTCF	chr19:41984200-41984350	A549	lung:	n/a	chr19:41984245-41984254 chr19:41984245-41984258
24	CTCF	chr19:41984280-41984430	HEK293	kidney:	n/a	n/a
25	CTCF	chr19:41982813-41982850	ProgFib	skin:	n/a	n/a
26	CUX1	chr19:42007456-42007659	K562	blood:	n/a	n/a
27	E2F4	chr19:42007189-42007607	MCF10A-Er-Src	breast:	n/a	n/a
28	E2F6	chr19:42007283-42007624	K562	blood:	n/a	n/a
29	E2F6	chr19:41986291-41986500	K562	blood:	n/a	n/a
30	E2F6	chr19:41986216-41986489	K562	blood:	n/a	n/a
31	E2F6	chr19:42006864-42008112	A549	lung:	n/a	n/a
32	E2F6	chr19:42006624-42008253	A549	lung:	n/a	n/a
33	E2F6	chr19:42007078-42007279	K562	blood:	n/a	n/a
34	E2F6	chr19:41985892-41986040	K562	blood:	n/a	n/a
35	EP300	chr19:41985848-41986019	K562	blood:	n/a	n/a
36	EP300	chr19:42007327-42007661	K562	blood:	n/a	n/a
37	FOS	chr19:41985798-41986124	MCF10A-Er-Src	breast:	n/a	chr19:41985971-41985982
38	FOS	chr19:42007233-42007722	HUVEC	blood vessel:	n/a	chr19:42007464-42007475
39	FOS	chr19:41985864-41986064	MCF10A-Er-Src	breast:	n/a	chr19:41985971-41985982
40	FOS	chr19:42007316-42007659	MCF10A-Er-Src	breast:	n/a	chr19:42007464-42007475
41	FOS	chr19:41984858-41986274	HUVEC	blood vessel:	n/a	chr19:41985971-41985982 chr19:41985559-41985568
42	FOS	chr19:41985870-41986108	MCF10A-Er-Src	breast:	n/a	chr19:41985971-41985982
43	FOS	chr19:41985833-41986024	MCF10A-Er-Src	breast:	n/a	chr19:41985971-41985982
44	FOS	chr19:42007323-42007645	MCF10A-Er-Src	breast:	n/a	chr19:42007464-42007475
45	FOS	chr19:42007874-42008336	MCF10A-Er-Src	breast:	n/a	n/a
46	FOS	chr19:42007303-42007652	MCF10A-Er-Src	breast:	n/a	chr19:42007464-42007475
47	FOS	chr19:42007322-42007647	MCF10A-Er-Src	breast:	n/a	chr19:42007464-42007475
48	FOSL1	chr19:42007197-42007840	HCT-116	colon:	n/a	n/a
49	FOSL1	chr19:42007174-42007932	HCT-116	colon:	n/a	n/a
50	FOSL2	chr19:42006817-42008108	A549	lung:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:42007378-42007428	GM12878	blood:	n/a
2	chr19:42007378-42007428	AG09319	gingival:	n/a
3	chr19:42007378-42007428	NT2-D1	testis:	n/a
4	chr19:42007378-42007428	HL-60	blood:	n/a
5	chr19:42007378-42007428	SKMC	muscle:	n/a
6	chr19:42007378-42007428	SK-N-SH	brain:	n/a
7	chr19:42007378-42007428	BE2_C	brain:	n/a
8	chr19:42007378-42007428	HCT-116	colon:	n/a
9	chr19:42007378-42007428	MCF-7	breast:	n/a
10	chr19:42007378-42007428	PFSK-1	brain:	n/a
11	chr19:42007378-42007428	Jurkat	blood:	n/a
12	chr19:42007378-42007428	IMR90	lung:	fetal
13	chr19:42007378-42007428	HMEC	breast:	n/a
14	chr19:42007378-42007428	SK-N-MC	brain:	n/a
15	chr19:42007378-42007428	Hepatocyte	liver:	n/a
16	chr19:42007378-42007428	HCPEpiC	choroid plexus:	n/a
17	chr19:42007378-42007428	HAEpiC	amniotic membrane:	n/a
18	chr19:42007378-42007428	GM12891	blood:	n/a
19	chr19:42007378-42007428	AoSMC	blood vessel:	n/a
20	chr19:42007378-42007428	GM06990	blood:	n/a
21	chr19:42007378-42007428	AG09309	skin:	n/a
22	chr19:42007378-42007428	NH-A	brain:	n/a
23	chr19:42007378-42007428	A549	lung:	n/a
24	chr19:42007378-42007428	HCF	heart:	n/a
25	chr19:42007378-42007428	MCF10A-Er-Src	breast:	n/a
26	chr19:42007378-42007428	HUVEC	blood vessel:	n/a
27	chr19:42007378-42007428	T-47D	breast:	n/a
28	chr19:42007378-42007428	Hela-S3	cervix:	n/a
29	chr19:42007378-42007428	HEEpiC	esophagus:	n/a
30	chr19:42007378-42007428	AG10803	skin:	n/a
31	chr19:42007378-42007428	ovcar-3	ovarian:	n/a
32	chr19:42007378-42007428	SK-N-SH_RA	brain:	n/a
33	chr19:42007378-42007428	NB4	blood:	n/a
34	chr19:42007378-42007428	RPTEC	kidney:	n/a
35	chr19:42007378-42007428	HIPEpiC	eye:	n/a
36	chr19:42007378-42007428	HRE	kidney:	n/a
37	chr19:42007378-42007428	HCM	heart:	n/a
38	chr19:42007378-42007428	U87	brain:	n/a
39	chr19:42007378-42007428	SAEC	small airway:	n/a
40	chr19:42007378-42007428	H1-hESC	embryonic stem cell:	embryo
41	chr19:42007378-42007428	CMK	blood:	n/a
42	chr19:42007378-42007428	PANC-1	pancreas:	n/a
43	chr19:42007378-42007428	HRPEpiC	eye:	n/a
44	chr19:42007378-42007428	AG04450	lung:	fetal
45	chr19:42007378-42007428	GM19239	blood:	n/a
46	chr19:42007378-42007428	ProgFib	skin:	n/a
47	chr19:42007378-42007428	K562	blood:	n/a
48	chr19:42007378-42007428	HepG2	liver:	n/a
49	chr19:42007378-42007428	HEK293	kidney:	embryo
50	chr19:42007378-42007428	HRCEpiC	kidney:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr19:41970790..41973417-chr19:42039173..42040939,2	K562	blood:
2	chr19:41979781..41981328-chr19:41984407..41987088,2	K562	blood:
3	chr19:41944061..41946977-chr19:42000429..42002001,2	K562	blood:
4	chr19:41945911..41947481-chr19:41988789..41990689,2	K562	blood:
5	chr19:41944280..41946189-chr19:42004239..42006678,2	K562	blood:

(count:27 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ATP5SL-1	chr19:42006494-42006554	ENSG00000249527
2	lnc-ATP5SL-1	chr19:42001210-42001335	ENSG00000267107.2
3	lnc-ATP5SL-1	chr19:41984451-41985192	NONHSAT066458
4	lnc-ATP5SL-1	chr19:42006494-42006540	NONHSAT066451
5	lnc-ATP5SL-1	chr19:41985040-41985192	NONHSAT066459
6	lnc-ATP5SL-1	chr19:42000448-42001335	ENSG00000267107.2
7	lnc-ATP5SL-1	chr19:42001210-42001335	NONHSAT066451
8	lnc-ATP5SL-1	chr19:41984989-41985192	ENSG00000249527
9	lnc-ATP5SL-1	chr19:41984989-41985051	ENSG00000267107.2
10	lnc-ATP5SL-1	chr19:42001210-42001335	NONHSAT066458
11	lnc-ATP5SL-1	chr19:41984989-41985192	NONHSAT066453
12	lnc-ATP5SL-1	chr19:41984451-41985192	NONHSAT066457
13	lnc-ATP5SL-1	chr19:42006494-42006554	NONHSAT066453
14	lnc-ATP5SL-1	chr19:41984989-41985049	ENSG00000267107.2
15	lnc-ATP5SL-1	chr19:42006494-42006554	ENSG00000249527
16	lnc-ATP5SL-1	chr19:41980371-41980444	ENSG00000267107.2
17	lnc-ATP5SL-1	chr19:41984989-41985192	NONHSAT066451
18	lnc-ATP5SL-1	chr19:42001210-42001338	NONHSAT066459
19	lnc-ATP5SL-1	chr19:41984989-41985192	ENSG00000249527
20	lnc-ATP5SL-1	chr19:41984989-41985049	ENSG00000267107.2
21	lnc-ATP5SL-1	chr19:42006494-42006545	NONHSAT066458
22	lnc-ATP5SL-1	chr19:42006494-42006554	ENSG00000267107.2
23	lnc-ATP5SL-1	chr19:42006494-42006538	NONHSAT066457
24	lnc-ATP5SL-1	chr19:42006494-42006559	ENSG00000249527
25	lnc-ATP5SL-1	chr19:41984989-41985192	ENSG00000267107.2
26	lnc-ATP5SL-1	chr19:42006494-42006539	ENSG00000267107.2
27	lnc-ATP5SL-1	chr19:42000448-42001335	ENSG00000249527

No data

Variant related genes	Relation type
ENSG00000267107	TF binding region
ENSG00000268034	TF binding region
ENSG00000267107	CpG island
ENSG00000268034	CpG island
ENSG00000267107	chromatin interactions
ENSG00000105341	chromatin interactions
SPTBN1	miRNA target sites
CHST11	miRNA target sites
EZH2	miRNA target sites
TMED7	miRNA target sites
PRSS21	miRNA target sites
CNN3	miRNA target sites

Extended variants
information (count: 1477 )
Associated
traits (count: 67 )

Variant overlapped rSNPs/rCNVs (count:1477 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs143022574	chr19:41972496-41972497	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs186461846	chr19:41972539-41972540	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs587729000	chr19:41972548-41972549	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs34190884	chr19:41972569-41972570	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs116188393	chr19:41972599-41972600	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs189968665	chr19:41972621-41972622	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs587742606	chr19:41972636-41972637	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs587624330	chr19:41972648-41972649	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs587698203	chr19:41972664-41972665	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs10416243	chr19:41972681-41972682	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs587654981	chr19:41972695-41972696	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs587683229	chr19:41972758-41972759	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs75797542	chr19:41972790-41972791	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs149972700	chr19:41972801-41972802	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs587708509	chr19:41972815-41972816	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs587627385	chr19:41972832-41972833	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs587656170	chr19:41972846-41972847	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs374404626	chr19:41972869-41972870	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs377441185	chr19:41972890-41972891	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs587672436	chr19:41972911-41972912	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs587730279	chr19:41972966-41972967	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs587612144	chr19:41973103-41973104	Bivalent/Poised TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs182292104	chr19:41973118-41973119	Bivalent/Poised TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs587749300	chr19:41973125-41973126	Bivalent/Poised TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs186568040	chr19:41973128-41973129	Bivalent/Poised TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs370194718	chr19:41973149-41973150	Bivalent/Poised TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs201378495	chr19:41973152-41973153	Bivalent/Poised TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs374940619	chr19:41973156-41973157	Bivalent/Poised TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs1987757	chr19:41973159-41973160	Bivalent/Poised TSS Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs376520932	chr19:41973180-41973181	Bivalent/Poised TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs587632674	chr19:41973188-41973189	Bivalent/Poised TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs370651632	chr19:41973192-41973193	Bivalent/Poised TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs201023545	chr19:41973354-41973355	Bivalent/Poised TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs587748449	chr19:41973442-41973443	Bivalent/Poised TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs73931501	chr19:41973485-41973486	Bivalent/Poised TSS Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs587674645	chr19:41973488-41973489	Bivalent/Poised TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs374044451	chr19:41973492-41973493	Bivalent/Poised TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs587773690	chr19:41973510-41973511	Bivalent/Poised TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs587657925	chr19:41973550-41973551	Bivalent/Poised TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs73931502	chr19:41973577-41973578	Bivalent/Poised TSS Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs587619164	chr19:41973599-41973600	Bivalent/Poised TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs201348964	chr19:41973609-41973610	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs58969690	chr19:41973660-41973661	Weak transcription	n/a	n/a	Overlapped CNVs	mRNA abundance
44	rs190875740	chr19:41973724-41973725	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs587608329	chr19:41973747-41973748	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs587664681	chr19:41973776-41973777	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs587745145	chr19:41973794-41973795	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs374535040	chr19:41973799-41973800	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs587679350	chr19:41973877-41973878	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs145201639	chr19:41973908-41973909	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:67)

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
Ovarian cancer	22174824	CNVD
Breast cancer	16608533	CNVD
Neuroblastoma	18923191	CNVD
Breast cancer	21364760	CNVD
Invasive pancreatic ductal carcinoma	18765526	CNVD
Rhabdomyosarcoma	16790082	CNVD
Chordoma	18071362	CNVD
Urothelial carcinoma	21177765	CNVD
small cell lung cancer	20016488	CNVD
Wilms tumour	21544195	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Ovarian neoplasms	16753589	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Metanephric adenoma	20802469	CNVD
Acute myeloid leukemia	16864856	CNVD
Bladder cancer	21909424	CNVD
Medulloblastoma	16783165	CNVD
Gastric cancer	18160780	CNVD
Hepatocellular carcinoma	16750200	CNVD
Basal cell lymphoma	19029149	CNVD
Breast cancer	20409316	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Multiple myeloma	16616336	CNVD
Renal cell carcinoma	18765545	CNVD
Acute myeloid leukemia	20729466	CNVD
Lung cancer	18438408	CNVD
Genital abnormality	22378287	CNVD
Hypospadia	22378287	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Astrocytoma	22246337	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:204 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:41968400-41982200	Weak transcription	HUVEC	blood vessel
2	chr19:41973000-41973600	Bivalent/Poised TSS	A549	lung
3	chr19:41976600-41976800	Bivalent Enhancer	Skeletal Muscle Male	skeletal muscle
4	chr19:41976600-41976800	Enhancers	Spleen	Spleen
5	chr19:41976800-41978800	Weak transcription	Spleen	Spleen
6	chr19:41978800-41979600	Enhancers	Spleen	Spleen
7	chr19:41979600-41982200	Weak transcription	Spleen	Spleen
8	chr19:41982200-41982400	Enhancers	Spleen	Spleen
9	chr19:41982200-41982800	Enhancers	GM12878-XiMat	blood
10	chr19:41982200-41983200	Enhancers	Primary B cells from peripheral blood	blood
11	chr19:41982200-41983400	Enhancers	HUVEC	blood vessel
12	chr19:41982400-41982800	Weak transcription	Spleen	Spleen
13	chr19:41982400-41983800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
14	chr19:41982800-41983000	Enhancers	Left Ventricle	heart
15	chr19:41982800-41983000	Enhancers	Right Atrium	heart
16	chr19:41982800-41983000	Enhancers	Spleen	Spleen
17	chr19:41982800-41983000	Flanking Active TSS	GM12878-XiMat	blood
18	chr19:41982800-41983600	Enhancers	Lung	lung
19	chr19:41983000-41983600	Genic enhancers	Left Ventricle	heart
20	chr19:41983000-41984000	Weak transcription	Right Atrium	heart
21	chr19:41983000-41986400	Weak transcription	Spleen	Spleen
22	chr19:41983400-41984000	Enhancers	Fetal Muscle Leg	muscle
23	chr19:41983400-41986400	Flanking Active TSS	HUVEC	blood vessel
24	chr19:41983600-41984200	Enhancers	Left Ventricle	heart
25	chr19:41983600-41985200	Active TSS	Lung	lung
26	chr19:41983800-41984600	Bivalent/Poised TSS	Fetal Muscle Trunk	muscle
27	chr19:41983800-41985000	Flanking Active TSS	Fetal Adrenal Gland	Adrenal Gland
28	chr19:41984000-41984200	Bivalent Enhancer	Adipose Nuclei	Adipose
29	chr19:41984000-41984200	Weak transcription	Fetal Muscle Leg	muscle
30	chr19:41984000-41984200	Enhancers	Right Atrium	heart
31	chr19:41984200-41984400	Bivalent/Poised TSS	Fetal Stomach	stomach
32	chr19:41984200-41984400	Flanking Active TSS	Left Ventricle	heart
33	chr19:41984200-41984800	Bivalent/Poised TSS	Right Ventricle	heart
34	chr19:41984200-41985000	Active TSS	Fetal Muscle Leg	muscle
35	chr19:41984200-41985600	Active TSS	Right Atrium	heart
36	chr19:41984200-41986400	Active TSS	Ovary	ovary
37	chr19:41984400-41984600	Active TSS	Adipose Nuclei	Adipose
38	chr19:41984400-41984800	Active TSS	Left Ventricle	heart
39	chr19:41984400-41985000	Active TSS	Fetal Stomach	stomach
40	chr19:41984400-41985000	Active TSS	Skeletal Muscle Male	skeletal muscle
41	chr19:41984600-41985000	Flanking Active TSS	Adipose Nuclei	Adipose
42	chr19:41984600-41985200	Active TSS	Fetal Muscle Trunk	muscle
43	chr19:41984800-41985000	Flanking Active TSS	Left Ventricle	heart
44	chr19:41984800-41985000	Flanking Active TSS	Right Ventricle	heart
45	chr19:41985000-41985400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
46	chr19:41985000-41986200	Weak transcription	Left Ventricle	heart
47	chr19:41985000-41986600	Enhancers	Adipose Nuclei	Adipose
48	chr19:41985000-41986600	Weak transcription	Skeletal Muscle Male	skeletal muscle
49	chr19:41985200-41985600	Weak transcription	Fetal Muscle Trunk	muscle
50	chr19:41985200-41986800	Weak transcription	Lung	lung

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