Variant report

Variant	nsv1055077
Chromosome Location	chr14:19002112-19606995
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3670)
CpG islands
(count:1099)
Chromatin interactive
region (count:3)
LncRNA
region (count:53)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:3670 , 50 per page) page: 1 2 3 4 5 6 7 ... 74

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr14:19108228-19108420	K562	blood:	n/a	n/a
2	ARID3A	chr14:19023877-19024245	K562	blood:	n/a	n/a
3	ATF1	chr14:19013231-19014316	K562	blood:	n/a	n/a
4	ATF1	chr14:19018922-19019306	K562	blood:	n/a	n/a
5	ATF1	chr14:19038969-19039342	K562	blood:	n/a	n/a
6	ATF1	chr14:19103184-19103383	K562	blood:	n/a	n/a
7	ATF1	chr14:19011340-19012104	K562	blood:	n/a	n/a
8	ATF1	chr14:19035201-19035489	K562	blood:	n/a	n/a
9	ATF1	chr14:19040731-19040981	K562	blood:	n/a	n/a
10	ATF1	chr14:19100486-19100700	K562	blood:	n/a	n/a
11	ATF1	chr14:19462190-19462538	K562	blood:	n/a	n/a
12	ATF1	chr14:19450073-19450214	K562	blood:	n/a	n/a
13	ATF1	chr14:19022998-19023337	K562	blood:	n/a	n/a
14	ATF1	chr14:19021205-19021751	K562	blood:	n/a	n/a
15	ATF1	chr14:19036176-19037332	K562	blood:	n/a	n/a
16	ATF1	chr14:19038248-19038629	K562	blood:	n/a	n/a
17	ATF1	chr14:19436953-19437483	K562	blood:	n/a	n/a
18	ATF1	chr14:19461425-19461537	K562	blood:	n/a	n/a
19	ATF1	chr14:19464826-19465023	K562	blood:	n/a	n/a
20	ATF1	chr14:19044418-19044791	K562	blood:	n/a	n/a
21	ATF1	chr14:19026382-19026765	K562	blood:	n/a	n/a
22	BACH1	chr14:19464051-19464239	K562	blood:	n/a	n/a
23	BACH1	chr14:19438368-19438886	K562	blood:	n/a	n/a
24	BACH1	chr14:19041796-19042864	K562	blood:	n/a	n/a
25	BACH1	chr14:19462184-19462510	K562	blood:	n/a	n/a
26	BACH1	chr14:19036232-19038897	K562	blood:	n/a	n/a
27	BACH1	chr14:19023871-19024248	K562	blood:	n/a	n/a
28	BATF	chr14:19016784-19017128	GM12878	blood:	n/a	n/a
29	BATF	chr14:19003781-19004656	GM12878	blood:	n/a	n/a
30	BATF	chr14:19016112-19016438	GM12878	blood:	n/a	n/a
31	BATF	chr14:19021813-19022107	GM12878	blood:	n/a	n/a
32	BATF	chr14:19022990-19023267	GM12878	blood:	n/a	n/a
33	BATF	chr14:19135407-19135704	GM12878	blood:	n/a	n/a
34	BATF	chr14:19007109-19007344	GM12878	blood:	n/a	n/a
35	BATF	chr14:19092736-19092938	GM12878	blood:	n/a	n/a
36	BATF	chr14:19010410-19010625	GM12878	blood:	n/a	n/a
37	BATF	chr14:19541484-19541694	GM12878	blood:	n/a	n/a
38	BATF	chr14:19032131-19032403	GM12878	blood:	n/a	n/a
39	BATF	chr14:19012766-19013020	GM12878	blood:	n/a	n/a
40	BATF	chr14:19136515-19136845	GM12878	blood:	n/a	n/a
41	BATF	chr14:19044988-19045347	GM12878	blood:	n/a	n/a
42	BATF	chr14:19008550-19008931	GM12878	blood:	n/a	n/a
43	BATF	chr14:19548118-19548363	GM12878	blood:	n/a	n/a
44	BATF	chr14:19036413-19036733	GM12878	blood:	n/a	n/a
45	BATF	chr14:19047189-19047418	GM12878	blood:	n/a	n/a
46	BATF	chr14:19013632-19013980	GM12878	blood:	n/a	n/a
47	BATF	chr14:19020415-19020830	GM12878	blood:	n/a	n/a
48	BATF	chr14:19041961-19042330	GM12878	blood:	n/a	n/a
49	BATF	chr14:19020424-19020768	GM12878	blood:	n/a	n/a
50	BATF	chr14:19041961-19042717	GM12878	blood:	n/a	n/a

(count:1099 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:19602149-19602199	HPAEpiC	pulmonary alveolar:	n/a
2	chr14:19602149-19602199	HPAEpiC	pulmonary alveolar:	n/a
3	chr14:19585143-19585193	HL-60	blood:	n/a
4	chr14:19110297-19110347	HCM	heart:	n/a
5	chr14:19360878-19360928	NT2-D1	testis:	n/a
6	chr14:19377109-19377159	HAEpiC	amniotic membrane:	n/a
7	chr14:19110297-19110347	HAEpiC	amniotic membrane:	n/a
8	chr14:19413192-19413242	IMR90	lung:	fetal
9	chr14:19109438-19109488	HMEC	breast:	n/a
10	chr14:19600442-19600492	HepG2	liver:	n/a
11	chr14:19594171-19594221	T-47D	breast:	n/a
12	chr14:19109768-19109818	BE2_C	brain:	n/a
13	chr14:19421688-19421738	NHBE	bronchial:	n/a
14	chr14:19109438-19109488	K562	blood:	n/a
15	chr14:19360878-19360928	HAEpiC	amniotic membrane:	n/a
16	chr14:19597077-19597127	HIPEpiC	eye:	n/a
17	chr14:19600442-19600492	SK-N-SH_RA	brain:	n/a
18	chr14:19109768-19109818	AG09309	skin:	n/a
19	chr14:19377109-19377159	GM12891	blood:	n/a
20	chr14:19109438-19109488	HCPEpiC	choroid plexus:	n/a
21	chr14:19413192-19413242	SAEC	small airway:	n/a
22	chr14:19602855-19602905	AG09319	gingival:	n/a
23	chr14:19602855-19602905	RPTEC	kidney:	n/a
24	chr14:19585143-19585193	HRCEpiC	kidney:	n/a
25	chr14:19110297-19110347	BJ	skin:	n/a
26	chr14:19422337-19422387	AG04449	skin:	fetal
27	chr14:19109768-19109818	SK-N-MC	brain:	n/a
28	chr14:19594171-19594221	HL-60	blood:	n/a
29	chr14:19562827-19562877	NHDF-neo	bronchial:	n/a
30	chr14:19402845-19402895	HAEpiC	amniotic membrane:	n/a
31	chr14:19360878-19360928	AG04449	skin:	fetal
32	chr14:19109438-19109488	H1-hESC	embryonic stem cell:	embryo
33	chr14:19360878-19360928	HCF	heart:	n/a
34	chr14:19360467-19360517	Hepatocyte	liver:	n/a
35	chr14:19553612-19553662	AG09319	gingival:	n/a
36	chr14:19562827-19562877	NB4	blood:	n/a
37	chr14:19562827-19562877	SKMC	muscle:	n/a
38	chr14:19600442-19600492	BE2_C	brain:	n/a
39	chr14:19602855-19602905	AG09309	skin:	n/a
40	chr14:19594171-19594221	Jurkat	blood:	n/a
41	chr14:19377109-19377159	Jurkat	blood:	n/a
42	chr14:19402845-19402895	HRCEpiC	kidney:	n/a
43	chr14:19110297-19110347	H1-hESC	embryonic stem cell:	embryo
44	chr14:19413192-19413242	GM06990	blood:	n/a
45	chr14:19602149-19602199	HCF	heart:	n/a
46	chr14:19109768-19109818	AG10803	skin:	n/a
47	chr14:19600442-19600492	SAEC	small airway:	n/a
48	chr14:19594171-19594221	AoSMC	blood vessel:	n/a
49	chr14:19360878-19360928	HPAEpiC	pulmonary alveolar:	n/a
50	chr14:19422337-19422387	HIPEpiC	eye:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr14:19023553..19024073-chr6:58778553..58779079,2	MCF-7	breast:
2	chr14:19022553..19024053-chr6:58774785..58777168,2	MCF-7	breast:
3	chr14:19019125..19019628-chr3:161087703..161088203,2	MCF-7	breast:

(count:53 , 50 per page) page: 1 2

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-POTEG-1	chr14:19530730-19530898	ENSG00000258265.1
2	lnc-POTEG-7	chr14:19603658-19603689	NONHSAT035463
3	lnc-OR11H12.1-6	chr14:19118171-19118336	NONHSAT035431
4	lnc-POTEG-6	chr14:19566012-19566082	NR_027480
5	lnc-POTEG-6	chr14:19561994-19562100	NR_027480
6	lnc-POTEG-6	chr14:19571348-19571418	NR_027480
7	lnc-POTEM-8	chr14:19563712-19564808	NR_046571
8	lnc-OR11H12.1-5	chr14:19195252-19195750	NONHSAT035433
9	lnc-OR11H12.1-2	chr14:19345173-19345267	NONHSAT035436
10	lnc-POTEM-8	chr14:19562689-19564808	ENSG00000258252
11	lnc-POTEG-7	chr14:19603204-19603279	NONHSAT035463
12	lnc-POTEG-6	chr14:19574186-19574352	NR_027480
13	lnc-OR11H12.1-2	chr14:19341921-19341993	NONHSAT035436
14	lnc-OR11H12.1-6	chr14:19114450-19114555	NONHSAT035431
15	lnc-POTEG-3	chr14:19606385-19606529	ENSG00000258314
16	lnc-POTEG-6	chr14:19584597-19584942	NR_027480
17	lnc-POTEG-6	chr14:19553365-19553937	NR_027480
18	lnc-POTEG-7	chr14:19597285-19597388	NONHSAT035463
19	lnc-POTEG-6	chr14:19558717-19558831	NR_027480
20	lnc-POTEM-8	chr14:19566286-19566680	NR_046571
21	lnc-POTEM-8	chr14:19563122-19564808	NR_110504
22	lnc-POTEM-10	chr14:19372736-19372787	ENSG00000257959.1
23	lnc-POTEM-9	chr14:19407015-19408008	NR_046104
24	lnc-POTEM-10	chr14:19332154-19332599	ENSG00000257959.1
25	lnc-POTEG-2	chr14:19517501-19517607	ENSG00000257891.1
26	lnc-POTEM-9	chr14:19409942-19410111	NR_046104
27	lnc-POTEG-1	chr14:19529958-19530169	ENSG00000258265.1
28	lnc-POTEG-2	chr14:19519800-19519837	ENSG00000257891.1
29	lnc-OR11H12.1-6	chr14:19117091-19117203	NONHSAT035431
30	lnc-OR11H12.1-1	chr14:19413561-19413898	ENSG00000258364.1
31	lnc-POTEG-9	chr14:19468509-19468885	NONHSAT035447
32	lnc-POTEM-8	chr14:19566286-19566680	NR_110504
33	lnc-POTEG-6	chr14:19558991-19559164	NR_027480
34	lnc-OR11H12.1-2	chr14:19339405-19339552	NONHSAT035436
35	lnc-POTEG-7	chr14:19595933-19596023	NONHSAT035463
36	lnc-POTEM-9	chr14:19406795-19408008	ENSG00000257504
37	lnc-POTEM-9	chr14:19409573-19409681	ENSG00000257504
38	lnc-POTEM-9	chr14:19409573-19409681	NR_046104
39	lnc-OR11H12.1-1	chr14:19412520-19412744	ENSG00000258364.1
40	lnc-POTEG-3	chr14:19605328-19606529	NONHSAT035465
41	lnc-POTEG-6	chr14:19578325-19578373	NR_027480
42	lnc-POTEG-6	chr14:19573100-19573144	NR_027480
43	lnc-POTEG-6	chr14:19563404-19563541	NR_027480
44	lnc-POTEM-15	chr14:19459200-19459267	NONHSAT035446
45	lnc-POTEG-7	chr14:19602828-19602942	NONHSAT035463
46	lnc-POTEM-9	chr14:19409942-19410111	ENSG00000257504
47	lnc-POTEG-6	chr14:19582971-19583089	NR_027480
48	lnc-POTEM-15	chr14:19458358-19458713	NONHSAT035446
49	lnc-POTEG-2	chr14:19515341-19515613	ENSG00000257891.1
50	lnc-OR11H12.1-6	chr14:19110203-19110377	NONHSAT035431

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	POTEG	hsa-miR-26b-5p	chr14:19563442-19563464

Variant related genes	Relation type
ENSG00000258265	TF binding region
ENSG00000257558	TF binding region
ENSG00000238442	TF binding region
ENSG00000258364	TF binding region
ENSG00000257504	TF binding region
ENSG00000257175	TF binding region
ENSG00000215398	TF binding region
ARHGAP42P5	TF binding region
ENSG00000258314	TF binding region
ENSG00000257731	TF binding region
ENSG00000257171	TF binding region
RNU6-1239P	TF binding region
ENSG00000258252	TF binding region
NF1P4	TF binding region
ENSG00000257825	TF binding region
ENSG00000257891	TF binding region
ENSG00000257959	TF binding region
ENSG00000258076	TF binding region
MED15P1	TF binding region
ENSG00000257635	TF binding region
ENSG00000257672	TF binding region
ENSG00000239200	TF binding region
RNU6-458P	TF binding region
ENSG00000257224	TF binding region
ENSG00000258367	TF binding region
ENSG00000257356	TF binding region
ENSG00000257721	TF binding region
ENSG00000257644	TF binding region
OR11H12	TF binding region
POTEG	TF binding region
ENSG00000258265	CpG island
ENSG00000257558	CpG island
ENSG00000238442	CpG island
ENSG00000258364	CpG island
ENSG00000257504	CpG island
ENSG00000257175	CpG island
ENSG00000215398	CpG island
ARHGAP42P5	CpG island
ENSG00000258314	CpG island
ENSG00000257731	CpG island
ENSG00000257171	CpG island
RNU6-1239P	CpG island
ENSG00000258252	CpG island
NF1P4	CpG island
ENSG00000257825	CpG island
ENSG00000257891	CpG island
ENSG00000257959	CpG island
ENSG00000258076	CpG island
MED15P1	CpG island
ENSG00000257635	CpG island
ENSG00000257672	CpG island
ENSG00000239200	CpG island
RNU6-458P	CpG island
ENSG00000257224	CpG island
ENSG00000258367	CpG island
ENSG00000257356	CpG island
ENSG00000257721	CpG island
ENSG00000257644	CpG island
OR11H12	CpG island
POTEG	CpG island

Extended variants
information (count: 9179 )
Associated
traits (count: 84 )

Variant overlapped rSNPs/rCNVs (count:9179 , 50 per page) page: 1 2 3 4 5 6 7 ... 184

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs185431939	chr14:19002146-19002147	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
2	rs139351967	chr14:19002161-19002162	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
3	rs144584321	chr14:19002163-19002164	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
4	rs138070262	chr14:19002166-19002167	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
5	rs141571320	chr14:19002168-19002169	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
6	rs143292361	chr14:19002169-19002170	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
7	rs59363733	chr14:19002172-19002173	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
8	rs137964732	chr14:19002185-19002186	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
9	rs150621531	chr14:19002188-19002189	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
10	rs200205524	chr14:19002191-19002192	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
11	rs370514389	chr14:19002242-19002243	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
12	rs28782840	chr14:19002253-19002254	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
13	rs58747419	chr14:19002254-19002255	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
14	rs565342041	chr14:19002255-19002256	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
15	rs61973536	chr14:19002262-19002263	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
16	rs532406891	chr14:19002264-19002265	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
17	rs544667084	chr14:19002265-19002266	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
18	rs61973537	chr14:19002269-19002270	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
19	rs199789787	chr14:19002271-19002272	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
20	rs189518222	chr14:19002278-19002279	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
21	rs61973538	chr14:19002292-19002293	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
22	rs77310295	chr14:19002294-19002295	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
23	rs562863926	chr14:19002298-19002299	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
24	rs530441660	chr14:19002307-19002308	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
25	rs375951349	chr14:19002326-19002327	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
26	rs368886770	chr14:19002330-19002331	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
27	rs61973539	chr14:19002331-19002332	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
28	rs548870540	chr14:19002334-19002335	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
29	rs61973540	chr14:19002343-19002344	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
30	rs61973541	chr14:19002355-19002356	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
31	rs112991057	chr14:19002371-19002372	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
32	rs183781047	chr14:19002378-19002379	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
33	rs199564170	chr14:19002379-19002380	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
34	rs201007315	chr14:19002384-19002385	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
35	rs201541424	chr14:19002393-19002394	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
36	rs546522736	chr14:19002403-19002404	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
37	rs188659268	chr14:19002404-19002405	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
38	rs567084566	chr14:19002423-19002424	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
39	rs59863341	chr14:19002426-19002427	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
40	rs527844190	chr14:19002437-19002438	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
41	rs368430918	chr14:19002441-19002442	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
42	rs551989110	chr14:19002469-19002470	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
43	rs112641324	chr14:19002474-19002475	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
44	rs570572076	chr14:19002484-19002485	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
45	rs28854877	chr14:19002497-19002498	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
46	rs372415349	chr14:19002504-19002505	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
47	rs75996874	chr14:19002556-19002557	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
48	rs555774798	chr14:19002572-19002573	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
49	rs112814864	chr14:19002584-19002585	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
50	rs61973543	chr14:19002611-19002612	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:84)

Disease	PMID	Source
Cancer	20164920	CNVD
Esophageal cancer	21851588	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
High-proliferative meningiomas	17937814	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Schizophrenia	21399695	CNVD
Cone-rod dystrophy	18421352	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Non-small cell lung cancer	21044232	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Melanoma	18172304	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Medulloblastoma	21979893	CNVD
Oral cancer	21386901	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Hepatocellular carcinoma	22174799	CNVD
Hepatocellular carcinoma	16750200	CNVD
Acute lymphoblastic leukemia	17640729	CNVD
Breast cancer	17899364	CNVD
Colorectal cancer	16774939	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Schizophrenia	20967226	CNVD
Autism	19287141	CNVD
early-passage human iPS cells	21368824	CNVD
Breast cancer	20932292	CNVD
Urothelial carcinoma	21177765	CNVD
Breast cancer	17142309	CNVD
Breast cancer	21364760	CNVD
Rett syndrome	21593744	CNVD
Breast cancer	20369283	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Incontinentia Pigmenti	22033527	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD
Myelofibrosis	22110671	CNVD
Alzheimer''s disease	21482944	CNVD
Mental retardation	19951919	CNVD
Neuroblastoma	21899760	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Heart disease	21282601	CNVD
Esophageal cancer	20955586	CNVD
Neurodevelopmental disorder	22521361	CNVD
Lung cancer	16773561	CNVD
Multiple myeloma	16616336	CNVD
Cancer	17440070	CNVD
Breast cancer	16272173	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Epilepsy	20736978	CNVD
Mental retardation	20736978	CNVD
severe speech impairment	20736978	CNVD
speech impairment	20736978	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Oligozoospermia	20877625	CNVD
Sertoli-cell only syndrome	20877625	CNVD
Ependymoma	20639864	CNVD
Williams Syndrome	20824207	CNVD
Developmental delay	21147756	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Pancreatic cancer	17952125	CNVD
Bladder cancer	21909424	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Renal cell carcinoma	21668985	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Prostate cancer	18632612	CNVD
Hodgkin''s lymphoma	17606441	CNVD

Chromatin state (count:555 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:19000400-19017400	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr14:19000600-19004400	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
3	chr14:19000600-19012800	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
4	chr14:19000600-19017200	ZNF genes & repeats	iPS-18 Cell Line	embryonic stem cell
5	chr14:19000600-19017800	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
6	chr14:19000600-19020200	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
7	chr14:19001200-19004000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
8	chr14:19001200-19004000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
9	chr14:19001200-19004000	Weak transcription	Aorta	Aorta
10	chr14:19001200-19004000	Weak transcription	Stomach Mucosa	stomach
11	chr14:19001200-19004000	Weak transcription	K562	blood
12	chr14:19001400-19002200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
13	chr14:19001400-19003000	Weak transcription	HUVEC	blood vessel
14	chr14:19001400-19003600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
15	chr14:19001400-19003800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
16	chr14:19001400-19003800	Weak transcription	NH-A	brain
17	chr14:19001400-19004000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr14:19001400-19004000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
19	chr14:19001400-19004000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
20	chr14:19001400-19004000	Weak transcription	Colon Smooth Muscle	Colon
21	chr14:19003000-19004200	ZNF genes & repeats	HUVEC	blood vessel
22	chr14:19003000-19004600	ZNF genes & repeats	Pancreatic Islets	Pancreatic Islet
23	chr14:19003000-19004800	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
24	chr14:19003200-19005200	ZNF genes & repeats	Primary hematopoietic stem cells	blood
25	chr14:19003400-19003600	Weak transcription	NHDF-Ad	bronchial
26	chr14:19003400-19005200	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
27	chr14:19003400-19007000	ZNF genes & repeats	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
28	chr14:19003600-19004400	ZNF genes & repeats	Psoas Muscle	Psoas
29	chr14:19003600-19004600	ZNF genes & repeats	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
30	chr14:19003600-19006600	ZNF genes & repeats	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
31	chr14:19003800-19004200	ZNF genes & repeats	Primary T killer memory cells from peripheral blood	blood
32	chr14:19003800-19004200	ZNF genes & repeats	Muscle Satellite Cultured Cells	--
33	chr14:19003800-19004200	ZNF genes & repeats	Small Intestine	intestine
34	chr14:19003800-19004400	ZNF genes & repeats	Brain Anterior Caudate	brain
35	chr14:19003800-19004400	ZNF genes & repeats	Brain Hippocampus Middle	brain
36	chr14:19003800-19004600	ZNF genes & repeats	Left Ventricle	heart
37	chr14:19003800-19005600	ZNF genes & repeats	Primary T cells from cord blood	blood
38	chr14:19003800-19005600	ZNF genes & repeats	NH-A	brain
39	chr14:19004000-19004200	ZNF genes & repeats	Primary hematopoietic stem cells short term culture	blood
40	chr14:19004000-19004200	ZNF genes & repeats	Primary T helper naive cells from peripheral blood	blood
41	chr14:19004000-19004200	Enhancers	Aorta	Aorta
42	chr14:19004000-19004200	ZNF genes & repeats	Brain Cingulate Gyrus	brain
43	chr14:19004000-19004200	ZNF genes & repeats	Brain Inferior Temporal Lobe	brain
44	chr14:19004000-19004200	ZNF genes & repeats	Colonic Mucosa	Colon
45	chr14:19004000-19004200	ZNF genes & repeats	Stomach Mucosa	stomach
46	chr14:19004000-19004200	ZNF genes & repeats	Dnd41	blood
47	chr14:19004000-19004200	ZNF genes & repeats	K562	blood
48	chr14:19004000-19004200	ZNF genes & repeats	Osteobl	bone
49	chr14:19004000-19004400	ZNF genes & repeats	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
50	chr14:19004000-19004400	ZNF genes & repeats	Primary T cells effector/memory enriched fromperipheralblood	blood

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