Variant report

Variant	esv1796470
Chromosome Location	chr19:39679379-39714631
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:871)
CpG islands
(count:1527)
Chromatin interactive
region (count:48)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:871 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr19:39695455-39695540	K562	blood:	n/a	n/a
2	ARID3A	chr19:39695822-39695965	K562	blood:	n/a	n/a
3	ATF1	chr19:39695455-39695815	K562	blood:	n/a	n/a
4	ATF3	chr19:39712607-39712845	K562	blood:	n/a	n/a
5	BACH1	chr19:39703059-39703329	H1-hESC	embryonic stem cell:	n/a	n/a
6	BCL3	chr19:39684408-39685102	A549	lung:	n/a	chr19:39684802-39684815
7	BCL3	chr19:39684339-39685037	A549	lung:	n/a	chr19:39684802-39684815
8	BCL3	chr19:39679251-39680318	A549	lung:	n/a	n/a
9	BCL3	chr19:39679308-39680241	A549	lung:	n/a	n/a
10	BCL3	chr19:39680922-39682067	A549	lung:	n/a	n/a
11	BHLHE40	chr19:39703056-39703213	K562	blood:	n/a	n/a
12	BHLHE40	chr19:39695466-39695797	K562	blood:	n/a	n/a
13	CBX3	chr19:39695703-39695981	K562	blood:	n/a	n/a
14	CBX3	chr19:39709790-39710233	HCT-116	colon:	n/a	n/a
15	CBX3	chr19:39692400-39692715	K562	blood:	n/a	n/a
16	CBX3	chr19:39706993-39707340	K562	blood:	n/a	n/a
17	CBX3	chr19:39687495-39687770	K562	blood:	n/a	n/a
18	CBX3	chr19:39703053-39703437	K562	blood:	n/a	n/a
19	CCNT2	chr19:39694710-39694935	K562	blood:	n/a	n/a
20	CCNT2	chr19:39687696-39687892	K562	blood:	n/a	n/a
21	CCNT2	chr19:39695431-39695913	K562	blood:	n/a	chr19:39695484-39695504 chr19:39695707-39695716 chr19:39695700-39695709
22	CEBPB	chr19:39689012-39689289	IMR90	lung:	n/a	n/a
23	CEBPB	chr19:39695763-39695934	A549	lung:	n/a	chr19:39695847-39695858
24	CEBPB	chr19:39684824-39684968	HepG2	liver:	n/a	n/a
25	CEBPB	chr19:39688869-39689204	MCF-7	breast:	n/a	n/a
26	CEBPB	chr19:39695606-39695972	K562	blood:	n/a	chr19:39695847-39695858
27	CEBPB	chr19:39685745-39686013	Hela-S3	cervix:	n/a	n/a
28	CEBPB	chr19:39712673-39712947	IMR90	lung:	n/a	chr19:39712789-39712800
29	CEBPB	chr19:39695598-39695984	K562	blood:	n/a	chr19:39695847-39695858
30	CEBPB	chr19:39688880-39689205	A549	lung:	n/a	n/a
31	CEBPB	chr19:39703149-39703448	A549	lung:	n/a	chr19:39703385-39703398
32	CEBPB	chr19:39681540-39681787	HepG2	liver:	n/a	chr19:39681640-39681651
33	CEBPB	chr19:39688343-39688383	A549	lung:	n/a	n/a
34	CEBPB	chr19:39698148-39698406	A549	lung:	n/a	chr19:39698299-39698310
35	CEBPB	chr19:39698146-39698385	HepG2	liver:	n/a	chr19:39698299-39698310
36	CEBPB	chr19:39698122-39698372	K562	blood:	n/a	chr19:39698299-39698310
37	CEBPB	chr19:39712632-39712945	HepG2	liver:	n/a	chr19:39712789-39712800
38	CEBPB	chr19:39682919-39683082	Hela-S3	cervix:	n/a	chr19:39683002-39683013
39	CEBPB	chr19:39682864-39683192	IMR90	lung:	n/a	chr19:39683002-39683013
40	CEBPB	chr19:39682910-39683048	HepG2	liver:	n/a	chr19:39683002-39683013
41	CEBPB	chr19:39682811-39683343	A549	lung:	n/a	chr19:39683002-39683013
42	CEBPB	chr19:39682832-39683199	K562	blood:	n/a	chr19:39683002-39683013
43	CEBPB	chr19:39712765-39712932	H1-hESC	embryonic stem cell:	n/a	chr19:39712789-39712800
44	CEBPB	chr19:39689043-39689287	Hela-S3	cervix:	n/a	n/a
45	CEBPB	chr19:39695637-39695921	K562	blood:	n/a	chr19:39695847-39695858
46	CEBPB	chr19:39688783-39689427	A549	lung:	n/a	n/a
47	CEBPB	chr19:39704062-39704196	A549	lung:	n/a	n/a
48	CEBPB	chr19:39688211-39688693	Hela-S3	cervix:	n/a	n/a
49	CEBPB	chr19:39695680-39695948	MCF-7	breast:	n/a	chr19:39695847-39695858
50	CEBPB	chr19:39689055-39689280	K562	blood:	n/a	n/a

(count:1527 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:39687568-39687618	HCT-116	colon:	n/a
2	chr19:39695237-39695287	NT2-D1	testis:	n/a
3	chr19:39687568-39687618	HCT-116	colon:	n/a
4	chr19:39695237-39695287	NT2-D1	testis:	n/a
5	chr19:39694617-39694667	NHDF-neo	bronchial:	n/a
6	chr19:39686695-39686745	SK-N-MC	brain:	n/a
7	chr19:39694709-39694759	GM19239	blood:	n/a
8	chr19:39695034-39695084	ProgFib	skin:	n/a
9	chr19:39687568-39687618	NB4	blood:	n/a
10	chr19:39691388-39691438	NHDF-neo	bronchial:	n/a
11	chr19:39695801-39695851	HCF	heart:	n/a
12	chr19:39692475-39692525	AG09319	gingival:	n/a
13	chr19:39687865-39687915	HCF	heart:	n/a
14	chr19:39694831-39694881	MCF10A-Er-Src	breast:	n/a
15	chr19:39687568-39687618	SKMC	muscle:	n/a
16	chr19:39687098-39687148	NT2-D1	testis:	n/a
17	chr19:39695237-39695287	CMK	blood:	n/a
18	chr19:39695011-39695061	HCPEpiC	choroid plexus:	n/a
19	chr19:39694831-39694881	SAEC	small airway:	n/a
20	chr19:39687865-39687915	HCT-116	colon:	n/a
21	chr19:39686583-39686633	HIPEpiC	eye:	n/a
22	chr19:39694617-39694667	NB4	blood:	n/a
23	chr19:39695065-39695115	ProgFib	skin:	n/a
24	chr19:39695237-39695287	A549	lung:	n/a
25	chr19:39694617-39694667	Caco-2	colon:	n/a
26	chr19:39687963-39688013	NH-A	brain:	n/a
27	chr19:39695065-39695115	Hepatocyte	liver:	n/a
28	chr19:39687963-39688013	CMK	blood:	n/a
29	chr19:39697154-39697204	HCF	heart:	n/a
30	chr19:39686583-39686633	CMK	blood:	n/a
31	chr19:39687079-39687129	GM12892	blood:	n/a
32	chr19:39694617-39694667	HCF	heart:	n/a
33	chr19:39694617-39694667	AG09319	gingival:	n/a
34	chr19:39694993-39695043	MCF-7	breast:	n/a
35	chr19:39691363-39691413	NB4	blood:	n/a
36	chr19:39691009-39691059	SK-N-SH	brain:	n/a
37	chr19:39696134-39696184	HUVEC	blood vessel:	n/a
38	chr19:39689909-39689959	AG10803	skin:	n/a
39	chr19:39695801-39695851	SK-N-MC	brain:	n/a
40	chr19:39689909-39689959	HAEpiC	amniotic membrane:	n/a
41	chr19:39691363-39691413	HAEpiC	amniotic membrane:	n/a
42	chr19:39694709-39694759	HEEpiC	esophagus:	n/a
43	chr19:39689909-39689959	CMK	blood:	n/a
44	chr19:39694617-39694667	NT2-D1	testis:	n/a
45	chr19:39695034-39695084	AG04450	lung:	fetal
46	chr19:39692475-39692525	SK-N-SH	brain:	n/a
47	chr19:39694709-39694759	SAEC	small airway:	n/a
48	chr19:39691388-39691438	AG04449	skin:	fetal
49	chr19:39697154-39697204	ECC-1	luminal epithelium:	n/a
50	chr19:39695034-39695084	PrEC	prostate:	n/a

(count:48 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr19:39600694..39601279-chr19:39688408..39689109,2	MCF-7	breast:
2	chr19:39656551..39660143-chr19:39675246..39681058,6	MCF-7	breast:
3	chr19:39699475..39701716-chr19:39889022..39890849,2	MCF-7	breast:
4	chr19:39521369..39524252-chr19:39683910..39686549,2	MCF-7	breast:
5	chr19:39610539..39613482-chr19:39683239..39685361,3	MCF-7	breast:
6	chr19:39676778..39680967-chr19:39681960..39686095,4	K562	blood:
7	chr19:39614408..39617809-chr19:39678152..39680089,3	MCF-7	breast:
8	chr19:39616787..39618305-chr19:39682159..39683750,2	MCF-7	breast:
9	chr19:39703112..39705306-chr19:39710340..39712292,2	K562	blood:
10	chr19:39687448..39690003-chr19:39693268..39695758,2	K562	blood:
11	chr19:39687448..39690003-chr19:39693268..39695758,2	K562	blood:
12	chr19:39703124..39705684-chr19:39814866..39817784,2	K562	blood:
13	chr19:39645920..39648679-chr19:39684558..39687537,2	MCF-7	breast:
14	chr19:39676778..39680967-chr19:39681960..39686095,4	K562	blood:
15	chr19:39684528..39687372-chr19:39688107..39690948,3	MCF-7	breast:
16	chr19:39665715..39668088-chr19:39693870..39695722,2	K562	blood:
17	chr19:39683585..39686543-chr19:39818875..39821716,2	MCF-7	breast:
18	chr19:39617069..39618976-chr19:39687926..39690455,2	MCF-7	breast:
19	chr19:39677174..39681975-chr19:39683439..39687085,6	MCF-7	breast:
20	chr19:39618887..39621010-chr19:39677122..39680092,2	MCF-7	breast:
21	chr19:39677174..39681975-chr19:39683439..39687085,6	MCF-7	breast:
22	chr19:39615742..39618240-chr19:39683167..39686406,3	MCF-7	breast:
23	chr19:39699114..39701619-chr19:39703320..39705265,2	K562	blood:
24	chr19:39695330..39697136-chr19:39901939..39904714,2	MCF-7	breast:
25	chr19:39703124..39706234-chr19:39814866..39817784,3	K562	blood:
26	chr19:39678151..39679810-chr19:39685956..39687541,2	MCF-7	breast:
27	chr19:39702433..39703702-chr19:39818478..39819662,6	MCF-7	breast:
28	chr19:39698828..39701571-chr19:39895887..39898728,2	K562	blood:
29	chr19:39694662..39698816-chr19:39700094..39703085,3	K562	blood:
30	chr19:39612566..39613389-chr19:39702383..39703279,2	MCF-7	breast:
31	chr19:39615011..39617919-chr19:39686746..39689965,3	MCF-7	breast:
32	chr19:39688505..39690542-chr19:39690963..39692607,2	K562	blood:
33	chr19:39694375..39697008-chr19:39898075..39900660,3	MCF-7	breast:
34	chr19:39622616..39624773-chr19:39692455..39694487,2	K562	blood:
35	chr19:39613319..39616155-chr19:39690923..39692457,2	K562	blood:
36	chr19:39678151..39679810-chr19:39685956..39687541,2	MCF-7	breast:
37	chr19:39699114..39701619-chr19:39703320..39705265,2	K562	blood:
38	chr19:39666393..39669331-chr19:39683166..39685486,2	K562	blood:
39	chr19:39689429..39690305-chr19:39818744..39819440,2	MCF-7	breast:
40	chr19:39676146..39678266-chr19:39679108..39681372,3	MCF-7	breast:
41	chr19:39614607..39616195-chr19:39688104..39689659,2	K562	blood:
42	chr19:39703112..39705306-chr19:39710340..39712292,2	K562	blood:
43	chr19:39669910..39671469-chr19:39677971..39680938,2	K562	blood:
44	chr19:39688505..39690542-chr19:39690963..39692607,2	K562	blood:
45	chr19:39690001..39692280-chr19:39837485..39839141,2	K562	blood:
46	chr19:39687919..39689922-chr19:39694303..39695815,2	MCF-7	breast:
47	chr19:39657621..39660070-chr19:39676796..39679772,2	MCF-7	breast:
48	chr19:39684528..39687372-chr19:39688107..39690948,3	MCF-7	breast:

No data

Variant related genes	Relation type
NCCRP1	TF binding region
SYCN	TF binding region
NCCRP1	CpG island
SYCN	CpG island
ENSG00000090924	chromatin interactions
ENSG00000188505	chromatin interactions
ENSG00000128016	chromatin interactions
ENSG00000179751	chromatin interactions
ENSG00000161243	chromatin interactions
ENSG00000266559	chromatin interactions
ENSG00000130669	chromatin interactions

Extended variants
information (count: 1224 )
Associated
traits (count: 66 )

Variant overlapped rSNPs/rCNVs (count:1224 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs8111473	chr19:39679379-39679380	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs565348822	chr19:39679412-39679413	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs139777017	chr19:39679414-39679415	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs188976601	chr19:39679450-39679451	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs144495094	chr19:39679469-39679470	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs181078295	chr19:39679472-39679473	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs185563284	chr19:39679473-39679474	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs542812439	chr19:39679524-39679525	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs561455252	chr19:39679532-39679533	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs189963182	chr19:39679538-39679539	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs180810055	chr19:39679558-39679559	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs368881811	chr19:39679559-39679560	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs565270853	chr19:39679575-39679576	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs537508421	chr19:39679577-39679578	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs186255236	chr19:39679611-39679612	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs80190291	chr19:39679645-39679646	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs527499261	chr19:39679655-39679656	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs375645137	chr19:39679657-39679658	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs201219941	chr19:39679670-39679671	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs397695468	chr19:39679673-39679674	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs548873851	chr19:39679676-39679677	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs368544625	chr19:39679697-39679698	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs78451373	chr19:39679741-39679742	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs537529637	chr19:39679756-39679757	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs114356381	chr19:39679762-39679763	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs570906509	chr19:39679794-39679795	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs538199950	chr19:39679811-39679812	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs76035864	chr19:39679813-39679814	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs191963788	chr19:39679835-39679836	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs370148474	chr19:39679903-39679904	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs113539546	chr19:39679927-39679928	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs145218738	chr19:39679945-39679946	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs116438713	chr19:39679970-39679971	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs554849494	chr19:39680014-39680015	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs557085769	chr19:39680103-39680104	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs543932418	chr19:39680121-39680122	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs559046983	chr19:39680226-39680227	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs4802023	chr19:39680259-39680260	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs532000239	chr19:39680301-39680302	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs60513822	chr19:39680311-39680312	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs113564002	chr19:39680315-39680316	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs183391513	chr19:39680376-39680377	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs536647813	chr19:39680381-39680382	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs542840183	chr19:39680387-39680388	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs528056537	chr19:39680449-39680450	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs375318388	chr19:39680455-39680456	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs112089216	chr19:39680457-39680458	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs560915271	chr19:39680480-39680481	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs531350494	chr19:39680509-39680510	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs8101586	chr19:39680537-39680538	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	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
Pleomorphic liposarcoma	18784837	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
Disorders of sex development	21048976	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
Mental retardation	19951919	CNVD
19q13.11 deletion syndrome	22378287	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	21045282	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Ovarian neoplasms	16753589	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Metanephric adenoma	20802469	CNVD
Acute myeloid leukemia	16864856	CNVD
Lung cancer	21569311	CNVD
Bladder cancer	21909424	CNVD
Medulloblastoma	16783165	CNVD
Breast cancer	21509527	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
Breast cancer	22522925	CNVD
Lung cancer	18438408	CNVD

Chromatin state (count:453 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:39657800-39687600	Weak transcription	Right Atrium	heart
2	chr19:39661400-39684600	Weak transcription	HSMM	muscle
3	chr19:39662600-39681800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr19:39663200-39681400	Weak transcription	Fetal Kidney	kidney
5	chr19:39667400-39679600	Weak transcription	HSMMtube	muscle
6	chr19:39669200-39685800	Weak transcription	NHEK	skin
7	chr19:39672000-39683600	Weak transcription	Pancreas	Pancrea
8	chr19:39672800-39683600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
9	chr19:39673000-39681400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
10	chr19:39673000-39684200	Weak transcription	Gastric	stomach
11	chr19:39673200-39681400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
12	chr19:39675400-39681800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
13	chr19:39678600-39681200	Weak transcription	A549	lung
14	chr19:39678600-39682000	Weak transcription	HUES6 Cell Line	embryonic stem cell
15	chr19:39678600-39684200	Weak transcription	Esophagus	oesophagus
16	chr19:39678600-39684400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
17	chr19:39678600-39687400	Weak transcription	Spleen	Spleen
18	chr19:39678800-39683400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
19	chr19:39679000-39679600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
20	chr19:39679600-39679800	Bivalent Enhancer	iPS DF 19.11 Cell Line	embryonic stem cell
21	chr19:39679600-39680000	Enhancers	HSMMtube	muscle
22	chr19:39679800-39684400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
23	chr19:39680000-39684600	Weak transcription	HSMMtube	muscle
24	chr19:39681200-39681400	Enhancers	A549	lung
25	chr19:39681400-39681600	Enhancers	Fetal Kidney	kidney
26	chr19:39681400-39681800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
27	chr19:39681400-39681800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
28	chr19:39681400-39681800	Flanking Active TSS	A549	lung
29	chr19:39681800-39682000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
30	chr19:39681800-39682000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
31	chr19:39681800-39682000	Enhancers	A549	lung
32	chr19:39682000-39683000	Weak transcription	A549	lung
33	chr19:39682000-39684600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
34	chr19:39682200-39683400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
35	chr19:39683000-39683200	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
36	chr19:39683000-39684400	Enhancers	A549	lung
37	chr19:39683000-39684600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
38	chr19:39683400-39684000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
39	chr19:39683400-39684800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
40	chr19:39683600-39683800	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
41	chr19:39683600-39683800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
42	chr19:39683600-39683800	Bivalent Enhancer	Brain Germinal Matrix	brain
43	chr19:39683600-39683800	Enhancers	HMEC	breast
44	chr19:39683600-39684400	Enhancers	Pancreas	Pancrea
45	chr19:39683800-39684200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
46	chr19:39683800-39686600	Weak transcription	HMEC	breast
47	chr19:39684200-39684800	Enhancers	Liver	Liver
48	chr19:39684200-39684800	Enhancers	Esophagus	oesophagus
49	chr19:39684200-39684800	Enhancers	Gastric	stomach
50	chr19:39684200-39684800	Enhancers	Stomach Mucosa	stomach

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