Variant report

Variant	nsv901831
Chromosome Location	chr14:44822128-44992259
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:514)
CpG islands
(count:184)
Chromatin interactive
region (count:27)
LncRNA
region (count:34)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:514 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr14:44918300-44918537	K562	blood:	n/a	n/a
2	BACH1	chr14:44862483-44862496	H1-hESC	embryonic stem cell:	n/a	n/a
3	BCL11A	chr14:44974131-44974349	GM12878	blood:	n/a	n/a
4	BHLHE40	chr14:44918215-44918640	K562	blood:	n/a	n/a
5	BHLHE40	chr14:44918841-44919166	HepG2	liver:	n/a	n/a
6	BHLHE40	chr14:44918875-44919187	HepG2	liver:	n/a	n/a
7	BRCA1	chr14:44887139-44887316	Hela-S3	cervix:	n/a	n/a
8	CCNT2	chr14:44918261-44918573	K562	blood:	n/a	n/a
9	CCNT2	chr14:44870973-44871349	K562	blood:	n/a	n/a
10	CEBPB	chr14:44865476-44865832	A549	lung:	n/a	chr14:44865665-44865674 chr14:44865621-44865632
11	CEBPB	chr14:44865547-44865773	H1-hESC	embryonic stem cell:	n/a	chr14:44865665-44865674 chr14:44865621-44865632
12	CEBPB	chr14:44892241-44892441	IMR90	lung:	n/a	chr14:44892371-44892382
13	CEBPB	chr14:44825168-44825407	HepG2	liver:	n/a	n/a
14	CEBPB	chr14:44860656-44860866	HepG2	liver:	n/a	chr14:44860752-44860763
15	CEBPB	chr14:44822861-44823165	K562	blood:	n/a	chr14:44823024-44823035
16	CEBPB	chr14:44865546-44865783	Hela-S3	cervix:	n/a	chr14:44865665-44865674 chr14:44865621-44865632
17	CEBPB	chr14:44822866-44823194	H1-hESC	embryonic stem cell:	n/a	chr14:44823024-44823035
18	CEBPB	chr14:44822884-44823206	A549	lung:	n/a	chr14:44823024-44823035
19	CEBPB	chr14:44957012-44957082	HepG2	liver:	n/a	chr14:44957022-44957033
20	CEBPB	chr14:44859620-44859752	H1-hESC	embryonic stem cell:	n/a	chr14:44859701-44859712
21	CEBPB	chr14:44859595-44859755	HepG2	liver:	n/a	chr14:44859701-44859712
22	CEBPB	chr14:44937993-44938273	Hela-S3	cervix:	n/a	chr14:44937995-44938006 chr14:44937995-44938008 chr14:44937995-44938008 chr14:44938138-44938149 chr14:44937995-44938008 chr14:44938159-44938170
23	CEBPB	chr14:44991866-44992131	HepG2	liver:	n/a	n/a
24	CEBPB	chr14:44822632-44823413	MCF-7	breast:	n/a	chr14:44823024-44823035
25	CEBPB	chr14:44865484-44865848	HepG2	liver:	n/a	chr14:44865665-44865674 chr14:44865621-44865632
26	CEBPB	chr14:44937997-44938297	A549	lung:	n/a	chr14:44938138-44938149 chr14:44938159-44938170
27	CEBPB	chr14:44822869-44823209	HepG2	liver:	n/a	chr14:44823024-44823035
28	CEBPB	chr14:44822857-44823212	IMR90	lung:	n/a	chr14:44823024-44823035
29	CEBPB	chr14:44822915-44823413	MCF-7	breast:	n/a	chr14:44823024-44823035
30	CEBPB	chr14:44932945-44933181	Hela-S3	cervix:	n/a	n/a
31	CEBPB	chr14:44892321-44892509	HepG2	liver:	n/a	chr14:44892371-44892382
32	CEBPB	chr14:44950479-44950667	A549	lung:	n/a	n/a
33	CEBPB	chr14:44865478-44865918	MCF-7	breast:	n/a	chr14:44865665-44865674 chr14:44865621-44865632
34	CEBPB	chr14:44937972-44938311	HepG2	liver:	n/a	chr14:44937995-44938006 chr14:44937995-44938008 chr14:44937995-44938008 chr14:44938138-44938149 chr14:44937995-44938008 chr14:44938159-44938170
35	CEBPB	chr14:44865449-44865776	MCF-7	breast:	n/a	chr14:44865665-44865674 chr14:44865621-44865632
36	CEBPB	chr14:44862132-44862411	HepG2	liver:	n/a	chr14:44862299-44862316 chr14:44862302-44862315
37	CEBPB	chr14:44979960-44980146	K562	blood:	n/a	n/a
38	CEBPB	chr14:44845840-44846035	A549	lung:	n/a	n/a
39	CEBPB	chr14:44865514-44865808	IMR90	lung:	n/a	chr14:44865665-44865674 chr14:44865621-44865632
40	CEBPD	chr14:44918203-44918635	K562	blood:	n/a	n/a
41	CEBPD	chr14:44918285-44918591	K562	blood:	n/a	n/a
42	CHD2	chr14:44979946-44980318	K562	blood:	n/a	n/a
43	CTCF	chr14:44838760-44838910	MCF-7	breast:	n/a	n/a
44	CTCF	chr14:44986742-44986802	Kidney_OC	kidney:	n/a	n/a
45	CTCF	chr14:44838660-44838952	MCF-7	breast:	n/a	n/a
46	CTCF	chr14:44922760-44922910	MCF-7	breast:	n/a	n/a
47	CTCF	chr14:44857548-44857591	GM13977	blood:	n/a	n/a
48	CTCF	chr14:44838750-44838851	Hela-S3	cervix:	n/a	n/a
49	CTCF	chr14:44974860-44975010	NB4	blood:	n/a	n/a
50	CTCF	chr14:44974940-44975049	H1-hESC	embryonic stem cell:	n/a	n/a

(count:184 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:44976457-44976507	ECC-1	luminal epithelium:	n/a
2	chr14:44976457-44976507	ECC-1	luminal epithelium:	n/a
3	chr14:44976457-44976507	HPAEpiC	pulmonary alveolar:	n/a
4	chr14:44976457-44976507	HepG2	liver:	n/a
5	chr14:44853952-44854002	HPAEpiC	pulmonary alveolar:	n/a
6	chr14:44853952-44854002	NHBE	bronchial:	n/a
7	chr14:44976457-44976507	HRE	kidney:	n/a
8	chr14:44976457-44976507	IMR90	lung:	fetal
9	chr14:44853952-44854002	A549	lung:	n/a
10	chr14:44976457-44976507	HIPEpiC	eye:	n/a
11	chr14:44976233-44976283	HL-60	blood:	n/a
12	chr14:44853952-44854002	Hepatocyte	liver:	n/a
13	chr14:44976457-44976507	GM19239	blood:	n/a
14	chr14:44853952-44854002	GM12892	blood:	n/a
15	chr14:44853952-44854002	SKMC	muscle:	n/a
16	chr14:44976457-44976507	Jurkat	blood:	n/a
17	chr14:44976457-44976507	PFSK-1	brain:	n/a
18	chr14:44976457-44976507	MCF10A-Er-Src	breast:	n/a
19	chr14:44976457-44976507	HRCEpiC	kidney:	n/a
20	chr14:44976457-44976507	AG09319	gingival:	n/a
21	chr14:44853952-44854002	HCF	heart:	n/a
22	chr14:44976233-44976283	BJ	skin:	n/a
23	chr14:44976457-44976507	HNPCEpiC	eye:	n/a
24	chr14:44976457-44976507	PANC-1	pancreas:	n/a
25	chr14:44853952-44854002	HEK293	kidney:	embryo
26	chr14:44976457-44976507	GM12892	blood:	n/a
27	chr14:44853952-44854002	HL-60	blood:	n/a
28	chr14:44976233-44976283	HRCEpiC	kidney:	n/a
29	chr14:44976233-44976283	GM12878	blood:	n/a
30	chr14:44853952-44854002	GM12891	blood:	n/a
31	chr14:44853952-44854002	HCT-116	colon:	n/a
32	chr14:44976457-44976507	Hepatocyte	liver:	n/a
33	chr14:44976233-44976283	HCPEpiC	choroid plexus:	n/a
34	chr14:44976233-44976283	GM06990	blood:	n/a
35	chr14:44976457-44976507	HEEpiC	esophagus:	n/a
36	chr14:44976233-44976283	Jurkat	blood:	n/a
37	chr14:44976233-44976283	ProgFib	skin:	n/a
38	chr14:44976233-44976283	U87	brain:	n/a
39	chr14:44976457-44976507	AG04449	skin:	fetal
40	chr14:44853952-44854002	HIPEpiC	eye:	n/a
41	chr14:44976457-44976507	HL-60	blood:	n/a
42	chr14:44853952-44854002	HCM	heart:	n/a
43	chr14:44976233-44976283	PANC-1	pancreas:	n/a
44	chr14:44976233-44976283	GM12892	blood:	n/a
45	chr14:44853952-44854002	CMK	blood:	n/a
46	chr14:44976457-44976507	K562	blood:	n/a
47	chr14:44976457-44976507	HCPEpiC	choroid plexus:	n/a
48	chr14:44976457-44976507	HCM	heart:	n/a
49	chr14:44976457-44976507	SK-N-SH_RA	brain:	n/a
50	chr14:44976457-44976507	BJ	skin:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr14:44838612..44839205-chr14:44974588..44975472,2	MCF-7	breast:
2	chr14:44838612..44839205-chr14:44974588..44975472,2	MCF-7	breast:
3	chr14:44856514..44860245-chr14:44862169..44864602,3	K562	blood:
4	chr14:44980118..44981638-chr17:41465259..41467724,2	MCF-7	breast:
5	chr14:44980118..44981638-chr17:41380370..41382247,2	MCF-7	breast:
6	chr14:44980119..44981639-chr17:41463633..41465366,4	MCF-7	breast:
7	chr14:44836359..44838272-chr14:44839234..44841841,3	K562	blood:
8	chr14:44978619..44981639-chr17:41463816..41468065,6	K562	blood:
9	chr14:44980139..44981640-chr17:41398653..41400867,3	K562	blood:
10	chr14:44836359..44838272-chr14:44839234..44841841,2	K562	blood:
11	chr14:44980137..44981640-chr17:41380487..41382264,3	K562	blood:
12	chr14:44922572..44923387-chr14:45126451..45127121,2	MCF-7	breast:
13	chr14:44838166..44839882-chr14:44873785..44875324,2	MCF-7	breast:
14	chr14:44978638..44981619-chrX:77931842..77933343,2	K562	blood:
15	chr14:44834762..44837688-chr14:44839758..44841386,2	MCF-7	breast:
16	chr14:44980118..44981640-chr17:41398653..41402673,7	K562	blood:
17	chr14:44836359..44838272-chr14:44839234..44841841,3	K562	blood:
18	chr14:44836359..44838272-chr14:44839234..44841841,2	K562	blood:
19	chr14:44838166..44839882-chr14:44873785..44875324,2	MCF-7	breast:
20	chr14:44838296..44838875-chr14:45126583..45127520,3	MCF-7	breast:
21	chr14:44834762..44837688-chr14:44839758..44841386,2	MCF-7	breast:
22	chr14:44980119..44981640-chr17:41463656..41466583,4	K562	blood:
23	chr14:44948272..44949206-chr8:143706277..143707059,2	MCF-7	breast:
24	chr1:17231477..17232007-chr14:44939008..44939528,2	Hela-S3	cervix:
25	chr11:62607619..62609217-chr14:44980118..44981639,2	K562	blood:
26	chr14:44857399..44860693-chr14:44862169..44864634,3	K562	blood:
27	chr14:44972455..44975189-chr14:45002674..45004244,2	MCF-7	breast:

(count:34 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FSCB-1	chr14:44915851-44915996	ENSG00000258487
2	lnc-FSCB-1	chr14:44861745-44861893	ENSG00000259126
3	lnc-FSCB-1	chr14:44913926-44914025	NONHSAT036608
4	lnc-FSCB-1	chr14:44862812-44862914	ENSG00000259126
5	lnc-FSCB-1	chr14:44936161-44936372	ENSG00000258487
6	lnc-FSCB-1	chr14:44913950-44914025	ENSG00000258487
7	lnc-FSCB-1	chr14:44947932-44948054	XLOC_011007
8	lnc-FSCB-1	chr14:44949713-44949820	ENSG00000258487
9	lnc-FSCB-1	chr14:44947932-44948054	XLOC_011007
10	lnc-FSCB-1	chr14:44862209-44862941	XLOC_011006
11	lnc-C14orf28-1	chr14:44977855-44977932	ENSG00000258747.1
12	lnc-FSCB-2	chr14:44853680-44853748	ENSG00000258969
13	lnc-FSCB-1	chr14:44936293-44936372	XLOC_011007
14	lnc-FSCB-1	chr14:44949713-44949833	XLOC_011007
15	lnc-C14orf28-1	chr14:44978530-44978686	ENSG00000258747.1
16	lnc-FSCB-1	chr14:44947932-44948054	NONHSAT036608
17	lnc-FSCB-1	chr14:44947921-44948054	XLOC_011007
18	lnc-FSCB-1	chr14:44949713-44949737	NONHSAT036608
19	lnc-FSCB-1	chr14:44913910-44914002	XLOC_011006
20	lnc-C14orf28-1	chr14:44978172-44978434	ENSG00000258747.1
21	lnc-C14orf28-1	chr14:44977855-44977932	NONHSAT036614
22	lnc-C14orf28-1	chr14:44976610-44976672	ENSG00000258747.1
23	lnc-FSCB-1	chr14:44949713-44949833	XLOC_011007
24	lnc-FSCB-1	chr14:44862821-44862919	ENSG00000259126
25	lnc-FSCB-1	chr14:44947932-44948054	ENSG00000258487
26	lnc-FSCB-1	chr14:44936162-44936372	XLOC_011007
27	lnc-FSCB-1	chr14:44861702-44861893	XLOC_011006
28	lnc-C14orf28-1	chr14:44976612-44976672	ENSG00000258747.1
29	lnc-FSCB-1	chr14:44949713-44949821	ENSG00000258487
30	lnc-FSCB-1	chr14:44862812-44862997	XLOC_011006
31	lnc-FSCB-1	chr14:44861734-44861893	ENSG00000259126
32	lnc-C14orf28-1	chr14:44976560-44976672	NONHSAT036614
33	lnc-FSCB-1	chr14:44947923-44948054	ENSG00000258487
34	lnc-C14orf28-1	chr14:44978206-44978434	ENSG00000258747.1

No data

Variant related genes	Relation type
FSCB	TF binding region
ENSG00000258487	TF binding region
ENSG00000258969	TF binding region
ENSG00000258747	TF binding region
ENSG00000259126	TF binding region
FSCB	CpG island
ENSG00000258487	CpG island
ENSG00000258969	CpG island
ENSG00000258747	CpG island
ENSG00000259126	CpG island
ENSG00000236383	chromatin interactions
ENSG00000133316	chromatin interactions
ENSG00000188825	chromatin interactions
ENSG00000259126	chromatin interactions
FAM134B	miRNA target sites
B4GALT1	miRNA target sites

Extended variants
information (count: 2515 )
Associated
traits (count: 58 )

Variant overlapped rSNPs/rCNVs (count:2515 , 50 per page) page: 1 2 3 4 5 6 7 ... 51

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs60580069	chr14:44837011-44837012	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs181292694	chr14:44837014-44837015	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs550172167	chr14:44837027-44837028	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs562312628	chr14:44837028-44837029	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs17615593	chr14:44837065-44837066	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs56162821	chr14:44837077-44837078	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs370785463	chr14:44837101-44837102	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs571756918	chr14:44837136-44837137	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs566549722	chr14:44837141-44837142	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs548860977	chr14:44837161-44837162	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs72121137	chr14:44837202-44837203	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs139433692	chr14:44837235-44837236	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs530994501	chr14:44837264-44837265	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs35122824	chr14:44837283-44837284	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs533791154	chr14:44837317-44837318	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs552354097	chr14:44837362-44837363	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs570769432	chr14:44837417-44837418	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs375707895	chr14:44837435-44837436	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs557412142	chr14:44837440-44837441	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs76973091	chr14:44837474-44837475	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs536635821	chr14:44837504-44837505	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs186756336	chr14:44837526-44837527	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs147080076	chr14:44837534-44837535	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs72684727	chr14:44837540-44837541	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs538306209	chr14:44837541-44837542	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs375837625	chr14:44837547-44837548	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs145065636	chr14:44837565-44837566	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs558688101	chr14:44837636-44837637	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs35830698	chr14:44837644-44837645	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs191152711	chr14:44837649-44837650	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs368473811	chr14:44837673-44837674	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs36096425	chr14:44837751-44837752	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs544477606	chr14:44837775-44837776	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs556189225	chr14:44837788-44837789	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs563179516	chr14:44837794-44837795	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs112151539	chr14:44837811-44837812	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs147743687	chr14:44837839-44837840	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs546989371	chr14:44837892-44837893	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs149231031	chr14:44837905-44837906	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs565664640	chr14:44837918-44837919	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs527340677	chr14:44837946-44837947	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs78602527	chr14:44838012-44838013	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs181035499	chr14:44838025-44838026	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs185239682	chr14:44838042-44838043	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs377758792	chr14:44838053-44838054	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs151303015	chr14:44838061-44838062	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs191130317	chr14:44838080-44838081	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs183259029	chr14:44838125-44838126	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs988473	chr14:44838216-44838217	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs115883597	chr14:44838219-44838220	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:58)

Disease	PMID	Source
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
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
Colorectal cancer	16774939	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	CNVD
Breast cancer	17899364	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
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Renal cell carcinoma	21668985	CNVD
Chronic myeloid leukemia	20724749	CNVD
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Wilms tumour	21544195	CNVD
Lung cancer	18438408	CNVD
Urothelial carcinoma	21177765	CNVD
Multiple myeloma	17550852	CNVD
Breast cancer	21785460	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	18632612	CNVD
small cell lung cancer	20016488	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	21858162	CNVD
Hirschsprung''s Disease	21712996	CNVD
Cancer	21183584	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Renal cell carcinoma	18194544	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	21364760	CNVD
Melanoma	17363583	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Williams Syndrome	20824207	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:120 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:44837000-44837400	Enhancers	Fetal Heart	heart
2	chr14:44837400-44839200	Weak transcription	Fetal Heart	heart
3	chr14:44838200-44839400	Enhancers	Fetal Intestine Large	intestine
4	chr14:44838200-44839600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr14:44838400-44842600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
6	chr14:44838600-44839400	Enhancers	NHEK	skin
7	chr14:44838800-44839200	Enhancers	HMEC	breast
8	chr14:44839200-44839600	Weak transcription	HMEC	breast
9	chr14:44839200-44840200	Enhancers	Fetal Heart	heart
10	chr14:44839400-44841200	Weak transcription	Fetal Intestine Large	intestine
11	chr14:44839600-44839800	Enhancers	HMEC	breast
12	chr14:44839600-44840000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
13	chr14:44839600-44840200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
14	chr14:44839600-44841400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
15	chr14:44839800-44841200	Weak transcription	HMEC	breast
16	chr14:44840200-44841200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
17	chr14:44840800-44842400	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
18	chr14:44841200-44841800	Enhancers	HMEC	breast
19	chr14:44841200-44842400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
20	chr14:44841200-44842600	Enhancers	Fetal Intestine Large	intestine
21	chr14:44841400-44841800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
22	chr14:44841800-44842400	Weak transcription	HMEC	breast
23	chr14:44842400-44842600	Enhancers	HMEC	breast
24	chr14:44843400-44850200	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
25	chr14:44845200-44846600	ZNF genes & repeats	Fetal Intestine Small	intestine
26	chr14:44848000-44849200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
27	chr14:44848400-44849200	Enhancers	Adipose Nuclei	Adipose
28	chr14:44849200-44851000	Weak transcription	Adipose Nuclei	Adipose
29	chr14:44849200-44851600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
30	chr14:44850200-44851000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
31	chr14:44851000-44852800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
32	chr14:44851000-44853600	Enhancers	Adipose Nuclei	Adipose
33	chr14:44851600-44853600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
34	chr14:44852600-44852800	Enhancers	Ovary	ovary
35	chr14:44852800-44853600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
36	chr14:44853000-44853600	Enhancers	Fetal Stomach	stomach
37	chr14:44853400-44853600	Enhancers	Ovary	ovary
38	chr14:44853400-44853800	Enhancers	Fetal Brain Female	brain
39	chr14:44853800-44857400	Weak transcription	Fetal Brain Female	brain
40	chr14:44854200-44854400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
41	chr14:44857400-44857600	Enhancers	Fetal Brain Female	brain
42	chr14:44861800-44862400	Enhancers	Fetal Intestine Large	intestine
43	chr14:44862400-44862800	Active TSS	Rectal Mucosa Donor 29	rectum
44	chr14:44872000-44872600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
45	chr14:44872000-44874400	Enhancers	Fetal Brain Male	brain
46	chr14:44872400-44874600	Enhancers	Fetal Brain Female	brain
47	chr14:44872600-44874000	Enhancers	Fetal Heart	heart
48	chr14:44873200-44874600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
49	chr14:44873400-44874400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
50	chr14:44873600-44874600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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