Variant report

Variant	nsv1036376
Chromosome Location	chr14:19002112-19706746
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:4704)
CpG islands
(count:1894)
Chromatin interactive
region (count:3)
LncRNA
region (count:138)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:4704 , 50 per page) page: 1 2 3 4 5 6 7 ... 95

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	chr14:19614565-19614964	K562	blood:	n/a	n/a
3	ARID3A	chr14:19023877-19024245	K562	blood:	n/a	n/a
4	ATF1	chr14:19035201-19035489	K562	blood:	n/a	n/a
5	ATF1	chr14:19022998-19023337	K562	blood:	n/a	n/a
6	ATF1	chr14:19036176-19037332	K562	blood:	n/a	n/a
7	ATF1	chr14:19038969-19039342	K562	blood:	n/a	n/a
8	ATF1	chr14:19464826-19465023	K562	blood:	n/a	n/a
9	ATF1	chr14:19609027-19609227	K562	blood:	n/a	n/a
10	ATF1	chr14:19044418-19044791	K562	blood:	n/a	n/a
11	ATF1	chr14:19461425-19461537	K562	blood:	n/a	n/a
12	ATF1	chr14:19040731-19040981	K562	blood:	n/a	n/a
13	ATF1	chr14:19103184-19103383	K562	blood:	n/a	n/a
14	ATF1	chr14:19614523-19614771	K562	blood:	n/a	n/a
15	ATF1	chr14:19100486-19100700	K562	blood:	n/a	n/a
16	ATF1	chr14:19462190-19462538	K562	blood:	n/a	n/a
17	ATF1	chr14:19436953-19437483	K562	blood:	n/a	n/a
18	ATF1	chr14:19619825-19620010	K562	blood:	n/a	n/a
19	ATF1	chr14:19697695-19697910	K562	blood:	n/a	n/a
20	ATF1	chr14:19038248-19038629	K562	blood:	n/a	n/a
21	ATF1	chr14:19450073-19450214	K562	blood:	n/a	n/a
22	ATF1	chr14:19610591-19610826	K562	blood:	n/a	n/a
23	ATF1	chr14:19013231-19014316	K562	blood:	n/a	n/a
24	ATF1	chr14:19011340-19012104	K562	blood:	n/a	n/a
25	ATF1	chr14:19021205-19021751	K562	blood:	n/a	n/a
26	ATF1	chr14:19018922-19019306	K562	blood:	n/a	n/a
27	ATF1	chr14:19026382-19026765	K562	blood:	n/a	n/a
28	ATF3	chr14:19614578-19614850	K562	blood:	n/a	n/a
29	BACH1	chr14:19041796-19042864	K562	blood:	n/a	n/a
30	BACH1	chr14:19036232-19038897	K562	blood:	n/a	n/a
31	BACH1	chr14:19464051-19464239	K562	blood:	n/a	n/a
32	BACH1	chr14:19608951-19609223	K562	blood:	n/a	n/a
33	BACH1	chr14:19462184-19462510	K562	blood:	n/a	n/a
34	BACH1	chr14:19614506-19614753	K562	blood:	n/a	n/a
35	BACH1	chr14:19023871-19024248	K562	blood:	n/a	n/a
36	BACH1	chr14:19438368-19438886	K562	blood:	n/a	n/a
37	BATF	chr14:19637495-19637851	GM12878	blood:	n/a	chr14:19637679-19637690
38	BATF	chr14:19012394-19013074	GM12878	blood:	n/a	n/a
39	BATF	chr14:19014433-19014827	GM12878	blood:	n/a	n/a
40	BATF	chr14:19135762-19136474	GM12878	blood:	n/a	n/a
41	BATF	chr14:19005011-19005385	GM12878	blood:	n/a	n/a
42	BATF	chr14:19546952-19547321	GM12878	blood:	n/a	n/a
43	BATF	chr14:19068281-19068796	GM12878	blood:	n/a	n/a
44	BATF	chr14:19007759-19008340	GM12878	blood:	n/a	n/a
45	BATF	chr14:19020424-19020768	GM12878	blood:	n/a	n/a
46	BATF	chr14:19009120-19009687	GM12878	blood:	n/a	n/a
47	BATF	chr14:19018765-19019271	GM12878	blood:	n/a	n/a
48	BATF	chr14:19016115-19016457	GM12878	blood:	n/a	n/a
49	BATF	chr14:19653590-19653843	GM12878	blood:	n/a	n/a
50	BATF	chr14:19013623-19014327	GM12878	blood:	n/a	n/a

(count:1894 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:19421688-19421738	NH-A	brain:	n/a
2	chr14:19613906-19613956	BE2_C	brain:	n/a
3	chr14:19594171-19594221	SKMC	muscle:	n/a
4	chr14:19421688-19421738	NH-A	brain:	n/a
5	chr14:19613906-19613956	BE2_C	brain:	n/a
6	chr14:19594171-19594221	SKMC	muscle:	n/a
7	chr14:19600442-19600492	Hepatocyte	liver:	n/a
8	chr14:19602855-19602905	HIPEpiC	eye:	n/a
9	chr14:19413192-19413242	PANC-1	pancreas:	n/a
10	chr14:19641452-19641502	AG04450	lung:	fetal
11	chr14:19686155-19686205	NB4	blood:	n/a
12	chr14:19600442-19600492	NB4	blood:	n/a
13	chr14:19110297-19110347	HL-60	blood:	n/a
14	chr14:19602149-19602199	SK-N-MC	brain:	n/a
15	chr14:19641452-19641502	SK-N-MC	brain:	n/a
16	chr14:19614556-19614606	K562	blood:	n/a
17	chr14:19686155-19686205	NH-A	brain:	n/a
18	chr14:19614556-19614606	LNCaP	prostate:	n/a
19	chr14:19597077-19597127	BJ	skin:	n/a
20	chr14:19641452-19641502	HEK293	kidney:	embryo
21	chr14:19585143-19585193	T-47D	breast:	n/a
22	chr14:19421688-19421738	GM19239	blood:	n/a
23	chr14:19597077-19597127	HEK293	kidney:	embryo
24	chr14:19585143-19585193	HepG2	liver:	n/a
25	chr14:19422337-19422387	HAEpiC	amniotic membrane:	n/a
26	chr14:19686670-19686720	GM06990	blood:	n/a
27	chr14:19402845-19402895	SAEC	small airway:	n/a
28	chr14:19614556-19614606	SK-N-MC	brain:	n/a
29	chr14:19602855-19602905	ECC-1	luminal epithelium:	n/a
30	chr14:19625820-19625870	SAEC	small airway:	n/a
31	chr14:19377109-19377159	HCPEpiC	choroid plexus:	n/a
32	chr14:19421688-19421738	BJ	skin:	n/a
33	chr14:19686670-19686720	HRPEpiC	eye:	n/a
34	chr14:19377109-19377159	IMR90	lung:	fetal
35	chr14:19597077-19597127	SK-N-SH_RA	brain:	n/a
36	chr14:19614556-19614606	NHBE	bronchial:	n/a
37	chr14:19686670-19686720	SK-N-MC	brain:	n/a
38	chr14:19594171-19594221	GM06990	blood:	n/a
39	chr14:19421688-19421738	GM12891	blood:	n/a
40	chr14:19110297-19110347	GM12891	blood:	n/a
41	chr14:19421688-19421738	Hepatocyte	liver:	n/a
42	chr14:19625154-19625204	MCF-7	breast:	n/a
43	chr14:19686672-19686722	MCF-7	breast:	n/a
44	chr14:19602149-19602199	SAEC	small airway:	n/a
45	chr14:19625154-19625204	NH-A	brain:	n/a
46	chr14:19109438-19109488	BJ	skin:	n/a
47	chr14:19360467-19360517	AG09309	skin:	n/a
48	chr14:19421688-19421738	HUVEC	blood vessel:	n/a
49	chr14:19602149-19602199	LNCaP	prostate:	n/a
50	chr14:19360467-19360517	H1-hESC	embryonic stem cell:	embryo

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

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

(count:138 , 50 per page) page: 1 2 3

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-POTEM-15	chr14:19459200-19459267	NONHSAT035446
2	lnc-POTEG-4	chr14:19653625-19653710	NONHSAT035478
3	lnc-POTEG-6	chr14:19558717-19558831	NR_027480
4	lnc-POTEM-7	chr14:19673473-19673623	ENSG00000228294
5	lnc-POTEG-3	chr14:19626361-19626451	NONHSAT035469
6	lnc-POTEG-4	chr14:19653893-19654004	ENSG00000225210
7	lnc-POTEG-4	chr14:19650037-19650126	ENSG00000225210
8	lnc-POTEG-4	chr14:19656089-19656224	ENSG00000225210
9	lnc-POTEG-4	chr14:19653893-19654004	ENSG00000225210
10	lnc-OR11H12.1-5	chr14:19195252-19195750	NONHSAT035433
11	lnc-POTEG-4	chr14:19683692-19684834	ENSG00000225210
12	lnc-POTEG-4	chr14:19691355-19691922	ENSG00000225210
13	lnc-POTEG-3	chr14:19611695-19611964	ENSG00000258314
14	lnc-POTEG-3	chr14:19643174-19643316	NONHSAT035469
15	lnc-POTEM-7	chr14:19680694-19681014	ENSG00000228294
16	lnc-POTEG-7	chr14:19595933-19596023	NONHSAT035463
17	lnc-POTEG-4	chr14:19650061-19650126	ENSG00000225210
18	lnc-POTEM-8	chr14:19563712-19564808	NR_046571
19	lnc-POTEG-3	chr14:19611768-19611964	ENSG00000258314.2
20	lnc-POTEG-3	chr14:19619448-19619513	NONHSAT035465
21	lnc-POTEG-1	chr14:19530730-19530898	ENSG00000258265.1
22	lnc-POTEM-9	chr14:19406795-19408008	ENSG00000257504
23	lnc-POTEM-7	chr14:19670792-19671105	XLOC_010962
24	lnc-POTEG-1	chr14:19529958-19530169	ENSG00000258265.1
25	lnc-OR11H12.1-6	chr14:19118171-19118336	NONHSAT035431
26	lnc-POTEG-4	chr14:19680595-19680685	ENSG00000225210
27	lnc-POTEG-4	chr14:19655734-19655871	ENSG00000225210
28	lnc-POTEG-4	chr14:19683027-19683250	ENSG00000225210
29	lnc-OR11H12.1-1	chr14:19413561-19413898	ENSG00000258364.1
30	lnc-POTEG-4	chr14:19653893-19654004	NR_110526
31	lnc-POTEG-4	chr14:19652244-19652354	ENSG00000225210
32	lnc-OR11H12.1-2	chr14:19339405-19339552	NONHSAT035436
33	lnc-POTEG-4	chr14:19655734-19655871	NR_110526
34	lnc-POTEG-7	chr14:19597285-19597388	NONHSAT035463
35	lnc-POTEG-6	chr14:19566012-19566082	NR_027480
36	lnc-POTEG-4	chr14:19650060-19650126	ENSG00000225210
37	lnc-POTEG-4	chr14:19653893-19654004	NONHSAT035478
38	lnc-POTEG-4	chr14:19652244-19652354	NONHSAT035478
39	lnc-OR11H12.1-1	chr14:19412520-19412744	ENSG00000258364.1
40	lnc-POTEG-6	chr14:19561994-19562100	NR_027480
41	lnc-POTEG-4	chr14:19653723-19653772	NONHSAT035478
42	lnc-POTEG-3	chr14:19619448-19619513	ENSG00000258314.2
43	lnc-POTEG-6	chr14:19563404-19563541	NR_027480
44	lnc-POTEM-7	chr14:19680694-19681016	XLOC_010962
45	lnc-POTEG-4	chr14:19650032-19650126	NR_110526
46	lnc-POTEG-4	chr14:19691355-19692916	NR_110526
47	lnc-POTEM-7	chr14:19678513-19678600	XLOC_010962
48	lnc-POTEM-9	chr14:19409573-19409681	NR_046104
49	lnc-POTEG-4	chr14:19656089-19656228	ENSG00000225210
50	lnc-POTEG-4	chr14:19691355-19691583	ENSG00000225210

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
ENSG00000257825	TF binding region
ENSG00000257891	TF binding region
GRAMD4P3	TF binding region
ENSG00000257959	TF binding region
ENSG00000258265	TF binding region
ENSG00000258076	TF binding region
ENSG00000257558	TF binding region
ENSG00000238442	TF binding region
ENSG00000258364	TF binding region
MED15P1	TF binding region
ENSG00000257635	TF binding region
ENSG00000257504	TF binding region
ENSG00000257175	TF binding region
ENSG00000257672	TF binding region
ENSG00000239200	TF binding region
ENSG00000215398	TF binding region
ENSG00000225210	TF binding region
ARHGAP42P5	TF binding region
RNU6-458P	TF binding region
ENSG00000258314	TF binding region
ENSG00000257224	TF binding region
ENSG00000257731	TF binding region
ENSG00000257171	TF binding region
ENSG00000258367	TF binding region
ENSG00000257356	TF binding region
RNU6-1239P	TF binding region
BMS1P17	TF binding region
ENSG00000257721	TF binding region
ENSG00000257644	TF binding region
ENSG00000258252	TF binding region
OR11H12	TF binding region
NF1P4	TF binding region
POTEG	TF binding region
DUXAP10	TF binding region
ENSG00000257825	CpG island
ENSG00000257891	CpG island
GRAMD4P3	CpG island
ENSG00000257959	CpG island
ENSG00000258265	CpG island
ENSG00000258076	CpG island
ENSG00000257558	CpG island
ENSG00000238442	CpG island
ENSG00000258364	CpG island
MED15P1	CpG island
ENSG00000257635	CpG island
ENSG00000257504	CpG island
ENSG00000257175	CpG island
ENSG00000257672	CpG island
ENSG00000239200	CpG island
ENSG00000215398	CpG island
ENSG00000225210	CpG island
ARHGAP42P5	CpG island
RNU6-458P	CpG island
ENSG00000258314	CpG island
ENSG00000257224	CpG island
ENSG00000257731	CpG island
ENSG00000257171	CpG island
ENSG00000258367	CpG island
ENSG00000257356	CpG island
RNU6-1239P	CpG island
BMS1P17	CpG island
ENSG00000257721	CpG island
ENSG00000257644	CpG island
ENSG00000258252	CpG island
OR11H12	CpG island
NF1P4	CpG island
POTEG	CpG island
DUXAP10	CpG island

Extended variants
information (count: 10048 )
Associated
traits (count: 87 )

Variant overlapped rSNPs/rCNVs (count:10048 , 50 per page) page: 1 2 3 4 5 6 7 ... 201

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:87)

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
Non-syndromic sensorineural hearing loss	19587683	CNVD
Glioma	20126413	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD

Chromatin state (count:601 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

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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