Variant report

Variant	nsv515536
Chromosome Location	chr19:36219525-36240960
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2530)
CpG islands
(count:2686)
Chromatin interactive
region (count:28)
LncRNA
region (count:52)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2530 , 50 per page) page: 1 2 3 4 5 6 7 ... 51

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr19:36230904-36231016	K562	blood:	n/a	n/a
2	ARID3A	chr19:36231909-36232068	K562	blood:	n/a	n/a
3	ARID3A	chr19:36235921-36236119	HepG2	liver:	n/a	n/a
4	ARID3A	chr19:36239077-36239686	K562	blood:	n/a	n/a
5	ARID3A	chr19:36235807-36236692	K562	blood:	n/a	n/a
6	ARID3A	chr19:36231370-36232278	HepG2	liver:	n/a	n/a
7	ATF1	chr19:36235703-36236645	K562	blood:	n/a	n/a
8	ATF1	chr19:36239075-36239572	K562	blood:	n/a	n/a
9	ATF1	chr19:36231337-36231801	K562	blood:	n/a	n/a
10	ATF2	chr19:36235518-36236039	H1-hESC	embryonic stem cell:	n/a	n/a
11	ATF2	chr19:36232924-36233606	GM12878	blood:	n/a	n/a
12	ATF2	chr19:36236007-36236610	H1-hESC	embryonic stem cell:	n/a	chr19:36236322-36236333
13	ATF2	chr19:36236152-36236678	H1-hESC	embryonic stem cell:	n/a	chr19:36236322-36236333
14	ATF2	chr19:36236187-36236560	GM12878	blood:	n/a	chr19:36236322-36236333
15	ATF2	chr19:36236126-36236716	GM12878	blood:	n/a	chr19:36236322-36236333
16	ATF2	chr19:36233014-36233622	GM12878	blood:	n/a	n/a
17	ATF2	chr19:36231631-36231984	GM12878	blood:	n/a	n/a
18	ATF2	chr19:36238983-36239554	GM12878	blood:	n/a	n/a
19	ATF2	chr19:36231482-36232101	GM12878	blood:	n/a	n/a
20	ATF3	chr19:36236179-36236575	K562	blood:	n/a	chr19:36236324-36236332 chr19:36236429-36236438
21	ATF3	chr19:36239096-36239378	K562	blood:	n/a	n/a
22	ATF3	chr19:36236003-36236764	A549	lung:	n/a	chr19:36236324-36236332 chr19:36236429-36236438
23	ATF3	chr19:36235508-36236824	A549	lung:	n/a	chr19:36236324-36236332 chr19:36236429-36236438
24	ATF3	chr19:36231172-36231991	A549	lung:	n/a	n/a
25	ATF3	chr19:36231160-36231977	A549	lung:	n/a	n/a
26	ATF3	chr19:36238804-36239979	A549	lung:	n/a	chr19:36239670-36239680
27	ATF3	chr19:36236202-36236484	K562	blood:	n/a	chr19:36236324-36236332 chr19:36236429-36236438
28	BACH1	chr19:36236308-36236563	H1-hESC	embryonic stem cell:	n/a	n/a
29	BACH1	chr19:36239341-36239900	H1-hESC	embryonic stem cell:	n/a	n/a
30	BACH1	chr19:36231186-36232152	H1-hESC	embryonic stem cell:	n/a	n/a
31	BACH1	chr19:36231198-36231391	K562	blood:	n/a	n/a
32	BATF	chr19:36233174-36233546	GM12878	blood:	n/a	n/a
33	BCL11A	chr19:36233108-36233605	GM12878	blood:	n/a	n/a
34	BCL11A	chr19:36233170-36233550	GM12878	blood:	n/a	n/a
35	BCL3	chr19:36238685-36239811	A549	lung:	n/a	chr19:36239253-36239261
36	BCL3	chr19:36235161-36237015	A549	lung:	n/a	chr19:36236330-36236339
37	BCL3	chr19:36235409-36236984	A549	lung:	n/a	chr19:36236330-36236339
38	BCL3	chr19:36233146-36233534	GM12878	blood:	n/a	n/a
39	BCL3	chr19:36228607-36229528	A549	lung:	n/a	n/a
40	BCL3	chr19:36229562-36231952	A549	lung:	n/a	chr19:36231101-36231108
41	BCL3	chr19:36229694-36232367	A549	lung:	n/a	chr19:36231101-36231108 chr19:36232113-36232121
42	BCL3	chr19:36230135-36230435	GM12878	blood:	n/a	n/a
43	BCL3	chr19:36238735-36240388	A549	lung:	n/a	chr19:36240281-36240290 chr19:36239253-36239261
44	BCLAF1	chr19:36233034-36233818	GM12878	blood:	n/a	n/a
45	BCLAF1	chr19:36235661-36236636	GM12878	blood:	n/a	chr19:36236330-36236339
46	BCLAF1	chr19:36233082-36233607	GM12878	blood:	n/a	n/a
47	BCLAF1	chr19:36238985-36239509	GM12878	blood:	n/a	chr19:36239253-36239261
48	BCLAF1	chr19:36231676-36232208	GM12878	blood:	n/a	chr19:36232113-36232121
49	BHLHE40	chr19:36231344-36232138	GM12878	blood:	n/a	n/a
50	BHLHE40	chr19:36235354-36236511	GM12878	blood:	n/a	n/a

(count:2686 , 50 per page) page: 1 2 3 4 5 6 7 ... 54

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:36236382-36236432	NH-A	brain:	n/a
2	chr19:36233469-36233519	AG10803	skin:	n/a
3	chr19:36236382-36236432	NH-A	brain:	n/a
4	chr19:36233469-36233519	AG10803	skin:	n/a
5	chr19:36232218-36232268	HMEC	breast:	n/a
6	chr19:36237863-36237913	GM12892	blood:	n/a
7	chr19:36232218-36232268	PFSK-1	brain:	n/a
8	chr19:36236150-36236200	SK-N-MC	brain:	n/a
9	chr19:36236539-36236589	SAEC	small airway:	n/a
10	chr19:36239208-36239258	NB4	blood:	n/a
11	chr19:36236496-36236546	HRCEpiC	kidney:	n/a
12	chr19:36236150-36236200	PrEC	prostate:	n/a
13	chr19:36236382-36236432	GM12891	blood:	n/a
14	chr19:36239588-36239638	GM06990	blood:	n/a
15	chr19:36236382-36236432	H1-hESC	embryonic stem cell:	embryo
16	chr19:36236336-36236386	HCT-116	colon:	n/a
17	chr19:36236547-36236597	GM19239	blood:	n/a
18	chr19:36232218-36232268	GM12878	blood:	n/a
19	chr19:36226397-36226447	HL-60	blood:	n/a
20	chr19:36233324-36233374	AG09309	skin:	n/a
21	chr19:36236454-36236504	HEEpiC	esophagus:	n/a
22	chr19:36239208-36239258	BJ	skin:	n/a
23	chr19:36234725-36234775	GM06990	blood:	n/a
24	chr19:36239797-36239847	HCPEpiC	choroid plexus:	n/a
25	chr19:36231413-36231463	RPTEC	kidney:	n/a
26	chr19:36228064-36228114	PANC-1	pancreas:	n/a
27	chr19:36228064-36228114	ProgFib	skin:	n/a
28	chr19:36229141-36229191	SK-N-MC	brain:	n/a
29	chr19:36226397-36226447	HNPCEpiC	eye:	n/a
30	chr19:36233380-36233430	GM12891	blood:	n/a
31	chr19:36239412-36239462	AG04449	skin:	fetal
32	chr19:36226397-36226447	ovcar-3	ovarian:	n/a
33	chr19:36236547-36236597	GM06990	blood:	n/a
34	chr19:36234725-36234775	HEK293	kidney:	embryo
35	chr19:36233380-36233430	HRCEpiC	kidney:	n/a
36	chr19:36231534-36231584	HCM	heart:	n/a
37	chr19:36239614-36239664	AoSMC	blood vessel:	n/a
38	chr19:36236393-36236443	NB4	blood:	n/a
39	chr19:36236539-36236589	BE2_C	brain:	n/a
40	chr19:36236393-36236443	HEK293	kidney:	embryo
41	chr19:36239208-36239258	PANC-1	pancreas:	n/a
42	chr19:36233447-36233497	HUVEC	blood vessel:	n/a
43	chr19:36235836-36235886	HPAEpiC	pulmonary alveolar:	n/a
44	chr19:36239412-36239462	AG04450	lung:	fetal
45	chr19:36231413-36231463	GM19239	blood:	n/a
46	chr19:36239455-36239505	LNCaP	prostate:	n/a
47	chr19:36236615-36236665	GM12892	blood:	n/a
48	chr19:36236393-36236443	HMEC	breast:	n/a
49	chr19:36239198-36239248	BE2_C	brain:	n/a
50	chr19:36239134-36239184	NHDF-neo	bronchial:	n/a

(count:28 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr19:36239350..36241235-chr19:36263074..36266129,3	MCF-7	breast:
2	chr19:36207379..36214815-chr19:36234227..36241330,25	MCF-7	breast:
3	chr19:36223600..36226210-chr19:36262533..36266105,3	K562	blood:
4	chr19:36223134..36225733-chr19:36234939..36237543,2	MCF-7	breast:
5	chr19:36234786..36236387-chr19:36265803..36268215,2	MCF-7	breast:
6	chr19:36035683..36038067-chr19:36234353..36237102,3	K562	blood:
7	chr19:36237682..36239540-chr19:36335176..36337549,2	MCF-7	breast:
8	chr19:36239210..36239818-chr20:3387776..3388665,2	NB4	blood:
9	chr19:36234932..36236574-chr19:36258515..36260489,2	K562	blood:
10	chr19:35759096..35761188-chr19:36236088..36238876,2	MCF-7	breast:
11	chr19:36239474..36241411-chr19:36265453..36267969,2	K562	blood:
12	chr19:36223134..36225733-chr19:36234939..36237543,2	MCF-7	breast:
13	chr19:36239375..36241509-chr19:36425781..36428099,2	MCF-7	breast:
14	chr19:36220761..36223012-chr19:36264330..36266140,2	MCF-7	breast:
15	chr19:36205476..36213390-chr19:36226310..36233646,27	MCF-7	breast:
16	chr19:36118469..36120275-chr19:36226530..36228193,2	K562	blood:
17	chr19:36234776..36236564-chr19:36265019..36266986,2	K562	blood:
18	chr19:36239415..36241356-chr19:36242820..36244877,2	MCF-7	breast:
19	chr19:36235922..36238148-chr19:36359346..36361404,2	MCF-7	breast:
20	chr16:28564909..28565793-chr19:36235985..36236487,2	Hela-S3	cervix:
21	chr19:36034766..36037168-chr19:36234979..36237516,2	MCF-7	breast:
22	chr19:36231818..36233362-chr19:36425701..36428426,2	MCF-7	breast:
23	chr11:64545307..64546190-chr19:36235841..36236593,2	Hela-S3	cervix:
24	chr19:36231491..36233720-chr19:36248400..36250494,2	MCF-7	breast:
25	chr19:36229002..36231040-chr19:36266877..36269774,2	MCF-7	breast:
26	chr19:36238866..36244880-chr19:36246037..36252437,21	MCF-7	breast:
27	chr19:36220754..36223608-chr19:36241225..36243043,2	MCF-7	breast:
28	chr19:35643125..35645834-chr19:36235394..36237704,2	K562	blood:

(count:52 , 50 per page) page: 1 2

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-HSPB6-1	chr19:36238126-36238382	ENSG00000267439.1
2	lnc-U2AF1L4-1	chr19:36236026-36236088	NR_110171
3	lnc-U2AF1L4-1	chr19:36235224-36235322	NR_110173
4	lnc-U2AF1L4-1	chr19:36233428-36233704	NR_110172
5	lnc-HSPB6-1	chr19:36239030-36239189	ENSG00000267439.1
6	lnc-U2AF1L4-1	chr19:36236249-36236343	NR_110171
7	lnc-U2AF1L4-3	chr19:36230725-36230989	NONHSAT065897
8	lnc-U2AF1L4-1	chr19:36233433-36234106	NONHSAT065900
9	lnc-U2AF1L4-1	chr19:36234971-36236113	NONHSAT065900
10	lnc-U2AF1L4-1	chr19:36234971-36235322	NONHSAT065899
11	lnc-U2AF1L4-3	chr19:36230429-36230527	NONHSAT065896
12	lnc-U2AF1L4-1	chr19:36234710-36234805	NONHSAT065900
13	lnc-U2AF1L4-1	chr19:36236026-36236088	NR_110172
14	lnc-U2AF1L4-1	chr19:36236249-36236327	NONHSAT065901
15	lnc-U2AF1L4-1	chr19:36234971-36235046	NR_110173
16	lnc-U2AF1L4-1	chr19:36234971-36235322	NONHSAT065901
17	lnc-U2AF1L4-1	chr19:36235696-36235882	NONHSAT065904
18	lnc-LIN37-2	chr19:36239468-36239659	NONHSAT065909
19	lnc-U2AF1L4-3	chr19:36231281-36231497	NONHSAT065897
20	lnc-U2AF1L4-1	chr19:36233428-36233704	NR_110171
21	lnc-U2AF1L4-3	chr19:36230611-36230670	NONHSAT065896
22	lnc-U2AF1L4-1	chr19:36236026-36236113	NR_110173
23	lnc-U2AF1L4-1	chr19:36235527-36235561	NONHSAT065899
24	lnc-U2AF1L4-3	chr19:36231281-36231450	NONHSAT065896
25	lnc-U2AF1L4-1	chr19:36234971-36235322	NR_110172
26	lnc-U2AF1L4-1	chr19:36234710-36234805	NR_110172
27	lnc-U2AF1L4-2	chr19:36231641-36232124	NONHSAT065898
28	lnc-U2AF1L4-1	chr19:36236026-36236254	NONHSAT065904
29	lnc-U2AF1L4-1	chr19:36236249-36236343	NR_110172
30	lnc-U2AF1L4-1	chr19:36234913-36235046	NR_110171
31	lnc-U2AF1L4-1	chr19:36235224-36235322	NR_110171
32	lnc-U2AF1L4-1	chr19:36236026-36236088	NONHSAT065901
33	lnc-U2AF1L4-1	chr19:36234710-36234805	NR_110171
34	lnc-U2AF1L4-1	chr19:36236249-36236343	NR_110173
35	lnc-U2AF1L4-1	chr19:36234710-36234805	NONHSAT065901
36	lnc-U2AF1L4-1	chr19:36233433-36233704	NONHSAT065901
37	lnc-U2AF1L4-1	chr19:36235527-36235639	NR_110172
38	lnc-HSPB6-1	chr19:36238146-36238382	ENSG00000247203
39	lnc-U2AF1L4-2	chr19:36233297-36233350	NONHSAT065898
40	lnc-U2AF1L4-1	chr19:36233428-36233704	NR_110173
41	lnc-U2AF1L4-1	chr19:36233430-36234805	NONHSAT065899
42	lnc-U2AF1L4-1	chr19:36236249-36236315	NONHSAT065902
43	lnc-U2AF1L4-1	chr19:36234710-36234805	NR_110173
44	lnc-U2AF1L4-1	chr19:36234056-36234246	NR_110171
45	lnc-U2AF1L4-1	chr19:36236249-36236303	NONHSAT065900
46	lnc-U2AF1L4-1	chr19:36235527-36235639	NONHSAT065901
47	lnc-U2AF1L4-1	chr19:36233434-36234805	NONHSAT065902
48	lnc-U2AF1L4-1	chr19:36235527-36235639	NR_110171
49	lnc-U2AF1L4-1	chr19:36234197-36234246	NONHSAT065900
50	lnc-HSPB6-1	chr19:36237958-36238382	ENSG00000267439.1

No data

Variant related genes	Relation type
PSENEN	TF binding region
U2AF1L4	TF binding region
ENSG00000267120	TF binding region
ENSG00000188223	TF binding region
IGFLR1	TF binding region
KMT2B	TF binding region
ENSG00000267328	TF binding region
ENSG00000267439	TF binding region
LIN37	TF binding region
PSENEN	CpG island
U2AF1L4	CpG island
ENSG00000267120	CpG island
ENSG00000188223	CpG island
IGFLR1	CpG island
KMT2B	CpG island
ENSG00000267328	CpG island
ENSG00000267439	CpG island
LIN37	CpG island
ENSG00000188223	chromatin interactions
ENSG00000088854	chromatin interactions
ENSG00000004777	chromatin interactions
ENSG00000176476	chromatin interactions
ENSG00000105677	chromatin interactions
ENSG00000105663	chromatin interactions
ENSG00000089327	chromatin interactions
ENSG00000168066	chromatin interactions
ENSG00000126254	chromatin interactions
ENSG00000267796	chromatin interactions
ENSG00000267120	chromatin interactions
ENSG00000205155	chromatin interactions
ENSG00000236144	chromatin interactions
ENSG00000161265	chromatin interactions
ENSG00000272333	chromatin interactions
ENSG00000161270	chromatin interactions
ENSG00000004776	chromatin interactions
ENSG00000105290	chromatin interactions
ENSG00000167595	chromatin interactions
ENSG00000126243	chromatin interactions
ENSG00000105698	chromatin interactions
ENSG00000267439	chromatin interactions
CDC42	miRNA target sites

Extended variants
information (count: 1174 )
Associated
traits (count: 62 )

Variant overlapped rSNPs/rCNVs (count:1174 , 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	rs8106959	chr19:36219525-36219526	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs551235234	chr19:36219581-36219582	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs200584088	chr19:36219593-36219594	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs571322620	chr19:36219594-36219595	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs536707369	chr19:36219618-36219619	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs142644094	chr19:36219623-36219624	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs376279284	chr19:36219635-36219636	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs372049345	chr19:36219675-36219676	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs566900387	chr19:36219681-36219682	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs375039138	chr19:36219693-36219694	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs201593055	chr19:36219702-36219703	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs555629405	chr19:36219705-36219706	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs372421332	chr19:36219709-36219710	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs572596532	chr19:36219717-36219718	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs377174050	chr19:36219726-36219727	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs369588398	chr19:36219739-36219740	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs191868666	chr19:36219765-36219766	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs377576838	chr19:36219774-36219775	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs2293684	chr19:36219800-36219801	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs146357202	chr19:36219807-36219808	Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs201037139	chr19:36219823-36219824	Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs182907764	chr19:36219844-36219845	Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs543905274	chr19:36219852-36219853	Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs79812110	chr19:36219871-36219872	Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs201133825	chr19:36219903-36219904	Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs370270196	chr19:36219921-36219922	Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs529292240	chr19:36219959-36219960	Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs374545872	chr19:36219996-36219997	Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs542986503	chr19:36220011-36220012	Strong transcription Weak transcription Transcr. at gene 5' and 3'	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs187709035	chr19:36220016-36220017	Strong transcription Weak transcription Transcr. at gene 5' and 3'	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs370802984	chr19:36220054-36220055	Strong transcription Weak transcription Transcr. at gene 5' and 3'	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs190936695	chr19:36220065-36220066	Strong transcription Weak transcription Transcr. at gene 5' and 3'	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs371880047	chr19:36220074-36220075	Strong transcription Weak transcription Transcr. at gene 5' and 3'	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs374382876	chr19:36220104-36220105	Strong transcription Weak transcription Transcr. at gene 5' and 3'	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs368307141	chr19:36220105-36220106	Strong transcription Weak transcription Transcr. at gene 5' and 3'	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs370642497	chr19:36220137-36220138	Strong transcription Weak transcription Transcr. at gene 5' and 3'	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs571320506	chr19:36220149-36220150	Strong transcription Weak transcription Transcr. at gene 5' and 3'	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs374717353	chr19:36220207-36220208	Weak transcription Strong transcription Transcr. at gene 5' and 3'	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs367744223	chr19:36220208-36220209	Weak transcription Strong transcription Transcr. at gene 5' and 3'	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs371458146	chr19:36220211-36220212	Weak transcription Strong transcription Transcr. at gene 5' and 3'	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs566962355	chr19:36220212-36220213	Weak transcription Strong transcription Transcr. at gene 5' and 3'	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs535841020	chr19:36220231-36220232	Weak transcription Strong transcription Transcr. at gene 5' and 3'	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs377273730	chr19:36220236-36220237	Weak transcription Strong transcription Transcr. at gene 5' and 3'	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs552503307	chr19:36220238-36220239	Weak transcription Strong transcription Transcr. at gene 5' and 3'	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs558535058	chr19:36220250-36220251	Weak transcription Strong transcription Transcr. at gene 5' and 3'	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs572295847	chr19:36220255-36220256	Weak transcription Strong transcription Transcr. at gene 5' and 3'	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs558350018	chr19:36220257-36220258	Weak transcription Strong transcription Transcr. at gene 5' and 3'	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs561265363	chr19:36220282-36220283	Weak transcription Strong transcription Transcr. at gene 5' and 3'	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs75055738	chr19:36220296-36220297	Weak transcription Strong transcription Transcr. at gene 5' and 3'	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs537578710	chr19:36220309-36220310	Weak transcription Strong transcription Transcr. at gene 5' and 3'	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:62)

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
Ovarian cancer	21397856	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Myelofibrosis	22110671	CNVD
Liver carcinoma	19366792	CNVD
Ovarian cancer	20844748	CNVD
Non-small cell lung cancer	21829676	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Chronic lymphocytic leukemia	21049055	CNVD
Cancer	21183584	CNVD
Honadal dysgenesis	21048976	CNVD
Neurodevelopmental disorder	22521361	CNVD
Endometrial cancer	23636398	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
Gastric cancer	21811585	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Glioma	17123091	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Multiple myeloma	16616336	CNVD
Lung cancer	21569311	CNVD
Breast cancer	21509527	CNVD

Chromatin state (count:2171 , 50 per page) page: 1 2 3 4 5 6 7 ... 44

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:36210600-36222400	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
2	chr19:36210600-36223000	Strong transcription	Fetal Lung	lung
3	chr19:36210600-36223000	Strong transcription	Rectal Smooth Muscle	rectum
4	chr19:36210600-36223400	Strong transcription	Primary T cells from cord blood	blood
5	chr19:36210600-36230000	Strong transcription	HUES64 Cell Line	embryonic stem cell
6	chr19:36210600-36230200	Strong transcription	HUES6 Cell Line	embryonic stem cell
7	chr19:36210600-36230200	Strong transcription	Cortex derived primary cultured neurospheres	brain
8	chr19:36210600-36230200	Strong transcription	Ovary	ovary
9	chr19:36210600-36230200	Strong transcription	Sigmoid Colon	Sigmoid Colon
10	chr19:36210600-36230400	Strong transcription	Brain Inferior Temporal Lobe	brain
11	chr19:36210600-36230400	Strong transcription	A549	lung
12	chr19:36210600-36230600	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
13	chr19:36210600-36230600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
14	chr19:36210600-36230600	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
15	chr19:36210600-36230600	Weak transcription	Right Atrium	heart
16	chr19:36210600-36230600	Strong transcription	NHLF	lung
17	chr19:36210600-36231200	Weak transcription	Fetal Brain Male	brain
18	chr19:36210800-36221800	Strong transcription	NHEK	skin
19	chr19:36210800-36223600	Strong transcription	Colon Smooth Muscle	Colon
20	chr19:36210800-36225000	Strong transcription	Fetal Muscle Trunk	muscle
21	chr19:36210800-36227400	Strong transcription	Primary B cells from peripheral blood	blood
22	chr19:36210800-36228000	Strong transcription	Fetal Thymus	thymus
23	chr19:36210800-36229600	Strong transcription	H1 Cell Line	embryonic stem cell
24	chr19:36210800-36229800	Strong transcription	Adipose Nuclei	Adipose
25	chr19:36210800-36230000	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
26	chr19:36210800-36230200	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
27	chr19:36210800-36230200	Strong transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
28	chr19:36210800-36230200	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
29	chr19:36210800-36230200	Strong transcription	Fetal Intestine Large	intestine
30	chr19:36210800-36230200	Strong transcription	Gastric	stomach
31	chr19:36210800-36230200	Strong transcription	Thymus	Thymus
32	chr19:36210800-36230400	Strong transcription	H9 Cell Line	embryonic stem cell
33	chr19:36210800-36230400	Strong transcription	Primary monocytes fromperipheralblood	blood
34	chr19:36210800-36230400	Strong transcription	Primary neutrophils fromperipheralblood	blood
35	chr19:36210800-36230400	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
36	chr19:36210800-36230400	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
37	chr19:36210800-36230400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
38	chr19:36210800-36230400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
39	chr19:36210800-36230400	Strong transcription	Brain Cingulate Gyrus	brain
40	chr19:36210800-36230400	Strong transcription	Brain Dorsolateral Prefrontal Cortex	brain
41	chr19:36210800-36230400	Strong transcription	Colonic Mucosa	Colon
42	chr19:36210800-36230600	Strong transcription	Primary hematopoietic stem cells short term culture	blood
43	chr19:36210800-36231000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
44	chr19:36211000-36221400	Strong transcription	Esophagus	oesophagus
45	chr19:36211000-36221600	Strong transcription	Placenta Amnion	Placenta Amnion
46	chr19:36211000-36223400	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
47	chr19:36211000-36225200	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
48	chr19:36211000-36227600	Strong transcription	Primary T helper cells fromperipheralblood	blood
49	chr19:36211000-36230000	Strong transcription	iPS-18 Cell Line	embryonic stem cell
50	chr19:36211000-36230000	Strong transcription	Left Ventricle	heart

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