Variant report

Variant	nsv470639
Chromosome Location	chr14:44319623-44750752
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1210)
CpG islands
(count:244)
Chromatin interactive
region (count:42)
LncRNA
region (count:11)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1210 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr14:44479441-44480344	HepG2	liver:	n/a	n/a
2	ARID3A	chr14:44369215-44370041	HepG2	liver:	n/a	n/a
3	ARID3A	chr14:44370996-44371623	HepG2	liver:	n/a	n/a
4	ARID3A	chr14:44368064-44368187	HepG2	liver:	n/a	n/a
5	BACH1	chr14:44632100-44632238	H1-hESC	embryonic stem cell:	n/a	n/a
6	BCL11A	chr14:44673306-44673565	H1-hESC	embryonic stem cell:	n/a	n/a
7	BCL11A	chr14:44342534-44342783	H1-hESC	embryonic stem cell:	n/a	n/a
8	BHLHE40	chr14:44361529-44361580	GM12878	blood:	n/a	n/a
9	BHLHE40	chr14:44369547-44369744	HepG2	liver:	n/a	n/a
10	BHLHE40	chr14:44435424-44435438	GM12878	blood:	n/a	n/a
11	BRCA1	chr14:44618833-44619126	H1-hESC	embryonic stem cell:	n/a	n/a
12	CEBPB	chr14:44675596-44675858	H1-hESC	embryonic stem cell:	n/a	n/a
13	CEBPB	chr14:44369517-44369811	HepG2	liver:	n/a	chr14:44369691-44369702
14	CEBPB	chr14:44444697-44444949	HepG2	liver:	n/a	chr14:44444844-44444855
15	CEBPB	chr14:44606738-44606986	HepG2	liver:	n/a	chr14:44606862-44606873
16	CEBPB	chr14:44364978-44365636	HepG2	liver:	n/a	n/a
17	CEBPB	chr14:44499216-44499416	H1-hESC	embryonic stem cell:	n/a	chr14:44499342-44499351 chr14:44499340-44499353 chr14:44499340-44499353 chr14:44499243-44499254 chr14:44499245-44499254 chr14:44499340-44499351
18	CEBPB	chr14:44478922-44479645	HepG2	liver:	n/a	chr14:44479481-44479494 chr14:44479483-44479494 chr14:44479481-44479492 chr14:44479481-44479494
19	CEBPB	chr14:44371059-44371372	HepG2	liver:	n/a	chr14:44371181-44371194 chr14:44371182-44371193
20	CEBPB	chr14:44499135-44499425	MCF-7	breast:	n/a	chr14:44499342-44499351 chr14:44499340-44499353 chr14:44499340-44499353 chr14:44499243-44499254 chr14:44499245-44499254 chr14:44499340-44499351
21	CEBPB	chr14:44560911-44561219	IMR90	lung:	n/a	chr14:44561060-44561071
22	CEBPB	chr14:44478922-44479578	IMR90	lung:	n/a	chr14:44479481-44479494 chr14:44479483-44479494 chr14:44479481-44479492 chr14:44479481-44479494
23	CEBPB	chr14:44606767-44606976	H1-hESC	embryonic stem cell:	n/a	chr14:44606862-44606873
24	CEBPB	chr14:44633192-44633496	Hela-S3	cervix:	n/a	chr14:44633351-44633362
25	CEBPB	chr14:44595859-44595978	A549	lung:	n/a	n/a
26	CEBPB	chr14:44487307-44487471	HepG2	liver:	n/a	n/a
27	CEBPB	chr14:44541354-44541571	HepG2	liver:	n/a	chr14:44541425-44541436
28	CEBPB	chr14:44479378-44479560	HepG2	liver:	n/a	chr14:44479481-44479494 chr14:44479483-44479494 chr14:44479481-44479492 chr14:44479481-44479494
29	CEBPB	chr14:44452992-44453227	ECC-1	luminal epithelium:	n/a	n/a
30	CEBPB	chr14:44599875-44600120	HepG2	liver:	n/a	chr14:44599949-44599960
31	CEBPB	chr14:44370974-44371424	MCF-7	breast:	n/a	chr14:44371181-44371194 chr14:44371182-44371193
32	CEBPB	chr14:44657629-44657829	H1-hESC	embryonic stem cell:	n/a	n/a
33	CEBPB	chr14:44319738-44319940	K562	blood:	n/a	chr14:44319833-44319844
34	CEBPB	chr14:44560981-44561240	A549	lung:	n/a	chr14:44561060-44561071
35	CEBPB	chr14:44448312-44448448	HepG2	liver:	n/a	chr14:44448367-44448378
36	CEBPB	chr14:44484998-44485226	HepG2	liver:	n/a	chr14:44485063-44485074
37	CEBPB	chr14:44479333-44479685	ECC-1	luminal epithelium:	n/a	chr14:44479481-44479494 chr14:44479483-44479494 chr14:44479481-44479492 chr14:44479481-44479494
38	CEBPB	chr14:44323921-44324167	HepG2	liver:	n/a	chr14:44324050-44324061 chr14:44324050-44324063 chr14:44324052-44324063 chr14:44324052-44324061
39	CEBPB	chr14:44633186-44633505	HepG2	liver:	n/a	chr14:44633351-44633362
40	CEBPB	chr14:44450644-44451128	HepG2	liver:	n/a	n/a
41	CEBPB	chr14:44499069-44499521	Hela-S3	cervix:	n/a	chr14:44499342-44499351 chr14:44499340-44499353 chr14:44499340-44499353 chr14:44499243-44499254 chr14:44499245-44499254 chr14:44499340-44499351
42	CEBPB	chr14:44719548-44719704	HepG2	liver:	n/a	chr14:44719600-44719611
43	CEBPB	chr14:44390701-44390897	HepG2	liver:	n/a	n/a
44	CEBPB	chr14:44560911-44561241	HepG2	liver:	n/a	chr14:44561060-44561071
45	CEBPB	chr14:44369433-44369870	HepG2	liver:	n/a	chr14:44369691-44369702
46	CEBPB	chr14:44487331-44487496	A549	lung:	n/a	n/a
47	CEBPB	chr14:44582232-44582510	Hela-S3	cervix:	n/a	n/a
48	CEBPB	chr14:44560929-44561184	K562	blood:	n/a	chr14:44561060-44561071
49	CEBPB	chr14:44605796-44606154	Hela-S3	cervix:	n/a	chr14:44605990-44606001 chr14:44605988-44606001 chr14:44605988-44605999 chr14:44605990-44606001
50	CEBPB	chr14:44369488-44369903	HepG2	liver:	n/a	chr14:44369691-44369702

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:44408417-44408467	A549	lung:	n/a
2	chr14:44408339-44408389	NHDF-neo	bronchial:	n/a
3	chr14:44408473-44408523	HEEpiC	esophagus:	n/a
4	chr14:44418808-44418858	IMR90	lung:	fetal
5	chr14:44408473-44408523	PrEC	prostate:	n/a
6	chr14:44408339-44408389	PrEC	prostate:	n/a
7	chr14:44408417-44408467	SKMC	muscle:	n/a
8	chr14:44408417-44408467	AoSMC	blood vessel:	n/a
9	chr14:44418808-44418858	GM19239	blood:	n/a
10	chr14:44408339-44408389	HCPEpiC	choroid plexus:	n/a
11	chr14:44408473-44408523	HCF	heart:	n/a
12	chr14:44408473-44408523	AG04450	lung:	fetal
13	chr14:44408339-44408389	H1-hESC	embryonic stem cell:	embryo
14	chr14:44418808-44418858	Jurkat	blood:	n/a
15	chr14:44408417-44408467	HCPEpiC	choroid plexus:	n/a
16	chr14:44418808-44418858	AG09319	gingival:	n/a
17	chr14:44408417-44408467	GM12892	blood:	n/a
18	chr14:44418808-44418858	HRCEpiC	kidney:	n/a
19	chr14:44418808-44418858	Hela-S3	cervix:	n/a
20	chr14:44418808-44418858	GM06990	blood:	n/a
21	chr14:44418808-44418858	ProgFib	skin:	n/a
22	chr14:44418808-44418858	PrEC	prostate:	n/a
23	chr14:44408339-44408389	PFSK-1	brain:	n/a
24	chr14:44408417-44408467	HAEpiC	amniotic membrane:	n/a
25	chr14:44408473-44408523	NHDF-neo	bronchial:	n/a
26	chr14:44408473-44408523	Hela-S3	cervix:	n/a
27	chr14:44408339-44408389	GM12891	blood:	n/a
28	chr14:44408339-44408389	CMK	blood:	n/a
29	chr14:44408473-44408523	HUVEC	blood vessel:	n/a
30	chr14:44418808-44418858	AoSMC	blood vessel:	n/a
31	chr14:44418808-44418858	CMK	blood:	n/a
32	chr14:44408473-44408523	LNCaP	prostate:	n/a
33	chr14:44408417-44408467	RPTEC	kidney:	n/a
34	chr14:44408473-44408523	K562	blood:	n/a
35	chr14:44418808-44418858	HCM	heart:	n/a
36	chr14:44408417-44408467	SK-N-SH_RA	brain:	n/a
37	chr14:44408473-44408523	A549	lung:	n/a
38	chr14:44408417-44408467	MCF10A-Er-Src	breast:	n/a
39	chr14:44408417-44408467	SK-N-MC	brain:	n/a
40	chr14:44408417-44408467	GM06990	blood:	n/a
41	chr14:44408417-44408467	HRCEpiC	kidney:	n/a
42	chr14:44408417-44408467	IMR90	lung:	fetal
43	chr14:44408473-44408523	CMK	blood:	n/a
44	chr14:44408339-44408389	GM06990	blood:	n/a
45	chr14:44408473-44408523	HEK293	kidney:	embryo
46	chr14:44408417-44408467	HPAEpiC	pulmonary alveolar:	n/a
47	chr14:44408417-44408467	SAEC	small airway:	n/a
48	chr14:44418808-44418858	HCT-116	colon:	n/a
49	chr14:44408417-44408467	SK-N-SH	brain:	n/a
50	chr14:44408473-44408523	SK-N-SH	brain:	n/a

(count:42 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr14:44606810..44610792-chr14:44612494..44615788,3	K562	blood:
2	chr14:44369406..44371311-chr14:44371355..44373381,2	MCF-7	breast:
3	chr14:44430928..44433388-chr14:44437033..44439809,2	MCF-7	breast:
4	chr14:44562970..44563903-chr14:44618440..44619350,3	MCF-7	breast:
5	chr14:44369406..44371311-chr14:44371355..44373381,2	MCF-7	breast:
6	chr14:44250330..44252060-chr14:44369516..44373246,3	MCF-7	breast:
7	chr14:44659162..44661192-chr14:44662497..44664945,3	MCF-7	breast:
8	chr14:43972805..43973364-chr14:44367745..44368249,2	MCF-7	breast:
9	chr14:44659162..44661192-chr14:44662497..44664945,3	MCF-7	breast:
10	chr14:44364361..44366552-chr14:44370416..44373233,2	MCF-7	breast:
11	chr14:44370633..44373508-chr14:44616084..44618482,2	MCF-7	breast:
12	chr14:44430928..44433388-chr14:44437033..44439809,2	MCF-7	breast:
13	chr14:44248792..44250657-chr14:44368815..44370864,2	MCF-7	breast:
14	chr14:44480170..44481920-chr14:44484152..44486382,2	MCF-7	breast:
15	chr14:44600217..44602036-chr14:44604194..44606588,2	K562	blood:
16	chr14:44364217..44368954-chr14:44370108..44373061,4	MCF-7	breast:
17	chr14:44606810..44610792-chr14:44612494..44615788,3	K562	blood:
18	chr11:64084683..64085194-chr14:44328405..44329034,2	MCF-7	breast:
19	chr14:44368312..44369942-chr14:44371630..44373482,2	MCF-7	breast:
20	chr14:44264520..44265214-chr14:44367667..44368353,2	MCF-7	breast:
21	chr1:149858085..149859649-chr14:44380057..44382174,2	MCF-7	breast:
22	chr14:44569949..44570449-chr8:101630587..101631141,2	MCF-7	breast:
23	chr14:44600217..44602036-chr14:44604194..44606588,2	K562	blood:
24	chr14:44370633..44373508-chr14:44616084..44618482,2	MCF-7	breast:
25	chr14:44363445..44365963-chr14:45603332..45605742,2	K562	blood:
26	chr14:44320172..44322382-chr14:44325472..44327926,2	K562	blood:
27	chr14:44370246..44372256-chr14:44617257..44619025,2	MCF-7	breast:
28	chr14:44368312..44369942-chr14:44371630..44373482,2	MCF-7	breast:
29	chr14:44370246..44372256-chr14:44617257..44619025,2	MCF-7	breast:
30	chr14:44480170..44481920-chr14:44484152..44486382,2	MCF-7	breast:
31	chr14:44320172..44322382-chr14:44325472..44327926,2	K562	blood:
32	chr14:44343776..44345372-chr14:44347119..44349752,2	K562	blood:
33	chr14:44429802..44430574-chr20:39327036..39327797,2	MCF-7	breast:
34	chr14:44364361..44366552-chr14:44370416..44373233,2	MCF-7	breast:
35	chr14:44372607..44374197-chr14:44383168..44385135,2	MCF-7	breast:
36	chr14:44118768..44119290-chr14:44370795..44371415,2	MCF-7	breast:
37	chr14:44343776..44345372-chr14:44347119..44349752,2	K562	blood:
38	chr14:44372607..44374197-chr14:44383168..44385135,2	MCF-7	breast:
39	chr14:44370894..44373377-chr14:44375088..44376684,2	MCF-7	breast:
40	chr14:44364217..44368954-chr14:44370108..44373061,4	MCF-7	breast:
41	chr14:44370894..44373377-chr14:44375088..44376684,2	MCF-7	breast:
42	chr14:44562970..44563903-chr14:44618440..44619350,3	MCF-7	breast:

(count:11 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FSCB-7	chr14:44546737-44547087	NONHSAT036603
2	lnc-FSCB-6	chr14:44621313-44621629	l_977_chr14:44621312-44622966_testes
3	lnc-FSCB-2	chr14:44518586-44518710	ENSG00000258969
4	lnc-FSCB-6	chr14:44622029-44622354	l_977_chr14:44621312-44622966_testes
5	lnc-FSCB-9	chr14:44336883-44336965	l_976_chr14:44304204-44307081_thyroid
6	lnc-FSCB-9	chr14:44326723-44326896	l_976_chr14:44304204-44307081_thyroid
7	lnc-FSCB-2	chr14:44464984-44465046	ENSG00000258969
8	lnc-FSCB-6	chr14:44621821-44621918	l_977_chr14:44621312-44622966_testes
9	lnc-FSCB-8	chr14:44477505-44479523	ucscGeneNc_uc001wvs_1
10	lnc-FSCB-9	chr14:44337342-44337506	l_976_chr14:44304204-44307081_thyroid
11	lnc-FSCB-6	chr14:44622425-44622966	l_977_chr14:44621312-44622966_testes

No data

Variant related genes	Relation type
ENSG00000259137	TF binding region
ENSG00000259019	TF binding region
ENSG00000259137	CpG island
ENSG00000259019	CpG island
ENSG00000229771	chromatin interactions
ENSG00000184678	chromatin interactions
ENSG00000173113	chromatin interactions
ENSG00000253740	chromatin interactions
ENSG00000100442	chromatin interactions
ENSG00000187790	chromatin interactions
ENSG00000178096	chromatin interactions
ENSG00000184270	chromatin interactions
ENSG00000184260	chromatin interactions
ENSG00000174226	chromatin interactions

Extended variants
information (count: 4947 )
Associated
traits (count: 70 )

Variant overlapped rSNPs/rCNVs (count:4947 , 50 per page) page: 1 2 3 4 5 6 7 ... 99

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs577733064	chr14:44321422-44321423	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs191177740	chr14:44321428-44321429	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs556933339	chr14:44321443-44321444	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs575483300	chr14:44321444-44321445	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs77390148	chr14:44321446-44321447	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs562043599	chr14:44321448-44321449	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs574119675	chr14:44321458-44321459	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs541506161	chr14:44321530-44321531	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs559819865	chr14:44321550-44321551	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs533318439	chr14:44321560-44321561	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs118068987	chr14:44321572-44321573	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs563771885	chr14:44321594-44321595	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs531086471	chr14:44321606-44321607	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs1952380	chr14:44321635-44321636	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs563224957	chr14:44321669-44321670	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs373303422	chr14:44321673-44321674	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs532299890	chr14:44321737-44321738	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs563648956	chr14:44321812-44321813	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs182599540	chr14:44321863-44321864	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs17243411	chr14:44321941-44321942	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs557114934	chr14:44321976-44321977	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs575540546	chr14:44322018-44322019	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs141329801	chr14:44322052-44322053	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs554920571	chr14:44322108-44322109	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs150357137	chr14:44322165-44322166	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs7154750	chr14:44322197-44322198	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs559548497	chr14:44322253-44322254	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs578042946	chr14:44322303-44322304	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs371741667	chr14:44322356-44322357	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs563889897	chr14:44322368-44322369	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs531024829	chr14:44322378-44322379	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs548665769	chr14:44322504-44322505	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs137973307	chr14:44322508-44322509	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs561246221	chr14:44322509-44322510	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs528034371	chr14:44322599-44322600	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs546563608	chr14:44322672-44322673	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs187700436	chr14:44322674-44322675	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs532213335	chr14:44322684-44322685	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs549499450	chr14:44322716-44322717	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs375665945	chr14:44322797-44322798	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs370281659	chr14:44322826-44322827	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs149487590	chr14:44322907-44322908	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs143855959	chr14:44322936-44322937	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs536476189	chr14:44323000-44323001	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs537457782	chr14:44323010-44323011	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs554857969	chr14:44323022-44323023	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs371507054	chr14:44323055-44323056	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs145159715	chr14:44323120-44323121	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs566783073	chr14:44323146-44323147	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs533883238	chr14:44323178-44323179	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:70)

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
Melanoma	17363583	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Mortal	21835882	CNVD
Breast cancer	21364760	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Pancreatic cancer	17952125	CNVD
Cancer	20164919	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Ovarian cancer	21781307	CNVD

Chromatin state (count:318 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:44321400-44321600	Enhancers	Fetal Brain Male	brain
2	chr14:44321600-44322600	Weak transcription	Fetal Brain Male	brain
3	chr14:44322600-44323000	Enhancers	Fetal Lung	lung
4	chr14:44322600-44323400	Enhancers	Fetal Brain Male	brain
5	chr14:44322800-44323000	Enhancers	Fetal Heart	heart
6	chr14:44323000-44324600	Weak transcription	Fetal Lung	lung
7	chr14:44323400-44324200	Weak transcription	Fetal Brain Male	brain
8	chr14:44324200-44326200	Enhancers	Fetal Brain Male	brain
9	chr14:44324600-44325200	Enhancers	Breast Myoepithelial Primary Cells	Breast
10	chr14:44324600-44325400	Enhancers	Fetal Lung	lung
11	chr14:44324800-44325200	Enhancers	Fetal Stomach	stomach
12	chr14:44324800-44325600	Enhancers	Fetal Heart	heart
13	chr14:44326400-44338600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
14	chr14:44328400-44328800	Enhancers	iPS-18 Cell Line	embryonic stem cell
15	chr14:44328400-44329000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
16	chr14:44328400-44329000	Enhancers	iPS-20b Cell Line	embryonic stem cell
17	chr14:44328600-44329000	Enhancers	HUES48 Cell Line	embryonic stem cell
18	chr14:44336800-44337000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr14:44337000-44338000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr14:44337800-44338200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
21	chr14:44338000-44338200	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr14:44338000-44338200	Enhancers	Pancreas	Pancrea
23	chr14:44338200-44341200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
24	chr14:44338600-44339000	Enhancers	ES-I3 Cell Line	embryonic stem cell
25	chr14:44338600-44339400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
26	chr14:44339000-44341000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
27	chr14:44339400-44341400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
28	chr14:44340000-44343000	Enhancers	Breast Myoepithelial Primary Cells	Breast
29	chr14:44340200-44341600	Enhancers	HUES6 Cell Line	embryonic stem cell
30	chr14:44340200-44341600	Enhancers	Pancreas	Pancrea
31	chr14:44340400-44340800	Enhancers	Fetal Heart	heart
32	chr14:44340600-44342000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
33	chr14:44340800-44341000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
34	chr14:44340800-44341800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
35	chr14:44340800-44342200	Weak transcription	Fetal Heart	heart
36	chr14:44340800-44343400	Enhancers	HUES64 Cell Line	embryonic stem cell
37	chr14:44341000-44341800	Enhancers	H9 Cell Line	embryonic stem cell
38	chr14:44341000-44342200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
39	chr14:44341000-44342600	Enhancers	H1 Cell Line	embryonic stem cell
40	chr14:44341000-44343200	Enhancers	ES-I3 Cell Line	embryonic stem cell
41	chr14:44341000-44343200	Enhancers	iPS-15b Cell Line	embryonic stem cell
42	chr14:44341200-44341400	Enhancers	iPS-20b Cell Line	embryonic stem cell
43	chr14:44341200-44341800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
44	chr14:44341200-44341800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
45	chr14:44341200-44343000	Enhancers	HUES48 Cell Line	embryonic stem cell
46	chr14:44341200-44343000	Enhancers	iPS-18 Cell Line	embryonic stem cell
47	chr14:44341400-44341800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
48	chr14:44341400-44342600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
49	chr14:44341400-44342800	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
50	chr14:44341600-44342000	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell

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