Variant report

Variant	nsv1014827
Chromosome Location	chr1:173653453-173692470
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:840)
CpG islands
(count:915)
Chromatin interactive
region (count:45)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

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No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:173683879-173684236	K562	blood:	n/a	n/a
2	ARID3A	chr1:173683740-173684218	HepG2	liver:	n/a	n/a
3	ARID3A	chr1:173686368-173686664	HepG2	liver:	n/a	n/a
4	ARID3A	chr1:173684431-173684448	HepG2	liver:	n/a	n/a
5	ATF2	chr1:173683763-173684374	GM12878	blood:	n/a	n/a
6	ATF2	chr1:173683768-173684263	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF2	chr1:173683716-173684266	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF2	chr1:173683785-173684282	GM12878	blood:	n/a	n/a
9	ATF3	chr1:173683783-173684367	A549	lung:	n/a	n/a
10	ATF3	chr1:173683731-173684348	A549	lung:	n/a	n/a
11	BACH1	chr1:173683815-173684274	K562	blood:	n/a	n/a
12	BATF	chr1:173683895-173684171	GM12878	blood:	n/a	n/a
13	BCL3	chr1:173683698-173684360	A549	lung:	n/a	chr1:173684255-173684263
14	BCL3	chr1:173683592-173684357	A549	lung:	n/a	chr1:173684255-173684263
15	BCLAF1	chr1:173683701-173684730	GM12878	blood:	n/a	chr1:173684255-173684263
16	BCLAF1	chr1:173683510-173684566	K562	blood:	n/a	chr1:173684255-173684263
17	BCLAF1	chr1:173683697-173684425	K562	blood:	n/a	chr1:173684255-173684263
18	BCLAF1	chr1:173683767-173684414	GM12878	blood:	n/a	chr1:173684255-173684263
19	BHLHE40	chr1:173683865-173684425	GM12878	blood:	n/a	n/a
20	BHLHE40	chr1:173660390-173660509	K562	blood:	n/a	n/a
21	BHLHE40	chr1:173683830-173684574	K562	blood:	n/a	n/a
22	BRCA1	chr1:173683877-173684260	HepG2	liver:	n/a	n/a
23	BRCA1	chr1:173683512-173684878	Hela-S3	cervix:	n/a	n/a
24	BRCA1	chr1:173683825-173684190	GM12878	blood:	n/a	n/a
25	CBX3	chr1:173657946-173658444	K562	blood:	n/a	n/a
26	CBX3	chr1:173683675-173684497	HCT-116	colon:	n/a	n/a
27	CBX3	chr1:173683491-173684665	K562	blood:	n/a	n/a
28	CBX3	chr1:173683570-173684488	K562	blood:	n/a	n/a
29	CCNT2	chr1:173683970-173684667	K562	blood:	n/a	n/a
30	CEBPB	chr1:173686401-173686647	A549	lung:	n/a	n/a
31	CEBPB	chr1:173683939-173684220	K562	blood:	n/a	n/a
32	CEBPB	chr1:173683699-173684683	Hela-S3	cervix:	n/a	n/a
33	CEBPB	chr1:173683712-173684618	GM12878	blood:	n/a	n/a
34	CEBPB	chr1:173683671-173684340	A549	lung:	n/a	n/a
35	CEBPB	chr1:173686284-173686637	Hela-S3	cervix:	n/a	chr1:173686295-173686306 chr1:173686293-173686306
36	CEBPB	chr1:173686271-173686693	HepG2	liver:	n/a	chr1:173686295-173686306 chr1:173686293-173686306
37	CEBPB	chr1:173683767-173684343	K562	blood:	n/a	n/a
38	CEBPB	chr1:173686209-173686406	K562	blood:	n/a	chr1:173686295-173686306 chr1:173686293-173686306
39	CEBPD	chr1:173683894-173684305	HepG2	liver:	n/a	n/a
40	CEBPD	chr1:173683794-173684654	K562	blood:	n/a	n/a
41	CHD1	chr1:173683594-173684562	GM12878	blood:	n/a	n/a
42	CHD2	chr1:173683676-173684535	GM12878	blood:	n/a	n/a
43	CHD2	chr1:173683862-173684714	HepG2	liver:	n/a	n/a
44	CHD2	chr1:173683758-173684839	Hela-S3	cervix:	n/a	n/a
45	CHD2	chr1:173683605-173684235	H1-hESC	embryonic stem cell:	n/a	n/a
46	CHD2	chr1:173683797-173684627	K562	blood:	n/a	n/a
47	CREB1	chr1:173683745-173684774	HepG2	liver:	n/a	n/a
48	CREB1	chr1:173683840-173684361	H1-hESC	embryonic stem cell:	n/a	n/a
49	CREB1	chr1:173683891-173684273	A549	lung:	n/a	n/a
50	CTCF	chr1:173660360-173660510	HMF	breast:	n/a	n/a

(count:915 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:173681595-173681645	AoSMC	blood vessel:	n/a
2	chr1:173683625-173683675	HNPCEpiC	eye:	n/a
3	chr1:173683938-173683988	K562	blood:	n/a
4	chr1:173683938-173683988	T-47D	breast:	n/a
5	chr1:173684020-173684070	HEEpiC	esophagus:	n/a
6	chr1:173681595-173681645	GM19239	blood:	n/a
7	chr1:173681595-173681645	H1-hESC	embryonic stem cell:	embryo
8	chr1:173683373-173683423	AG09309	skin:	n/a
9	chr1:173681595-173681645	NB4	blood:	n/a
10	chr1:173683625-173683675	HEEpiC	esophagus:	n/a
11	chr1:173684020-173684070	SKMC	muscle:	n/a
12	chr1:173684386-173684436	NB4	blood:	n/a
13	chr1:173684007-173684057	GM12892	blood:	n/a
14	chr1:173684045-173684095	LNCaP	prostate:	n/a
15	chr1:173684020-173684070	AoSMC	blood vessel:	n/a
16	chr1:173683890-173683940	HL-60	blood:	n/a
17	chr1:173684474-173684524	NHDF-neo	bronchial:	n/a
18	chr1:173684045-173684095	HEK293	kidney:	embryo
19	chr1:173684007-173684057	ECC-1	luminal epithelium:	n/a
20	chr1:173684675-173684725	HUVEC	blood vessel:	n/a
21	chr1:173685201-173685251	HAEpiC	amniotic membrane:	n/a
22	chr1:173682610-173682660	NH-A	brain:	n/a
23	chr1:173684007-173684057	HAEpiC	amniotic membrane:	n/a
24	chr1:173683938-173683988	HRCEpiC	kidney:	n/a
25	chr1:173682610-173682660	LNCaP	prostate:	n/a
26	chr1:173683890-173683940	Jurkat	blood:	n/a
27	chr1:173685201-173685251	U87	brain:	n/a
28	chr1:173684561-173684611	A549	lung:	n/a
29	chr1:173684561-173684611	SK-N-SH_RA	brain:	n/a
30	chr1:173684045-173684095	NH-A	brain:	n/a
31	chr1:173683890-173683940	HepG2	liver:	n/a
32	chr1:173684045-173684095	NHBE	bronchial:	n/a
33	chr1:173684675-173684725	AoSMC	blood vessel:	n/a
34	chr1:173684561-173684611	HRPEpiC	eye:	n/a
35	chr1:173684386-173684436	PANC-1	pancreas:	n/a
36	chr1:173684561-173684611	HRCEpiC	kidney:	n/a
37	chr1:173683625-173683675	NH-A	brain:	n/a
38	chr1:173684386-173684436	MCF10A-Er-Src	breast:	n/a
39	chr1:173684386-173684436	GM12878	blood:	n/a
40	chr1:173684595-173684645	SK-N-MC	brain:	n/a
41	chr1:173684020-173684070	ProgFib	skin:	n/a
42	chr1:173684020-173684070	NT2-D1	testis:	n/a
43	chr1:173684595-173684645	HEEpiC	esophagus:	n/a
44	chr1:173683938-173683988	SK-N-SH	brain:	n/a
45	chr1:173684474-173684524	H1-hESC	embryonic stem cell:	embryo
46	chr1:173684675-173684725	PFSK-1	brain:	n/a
47	chr1:173684675-173684725	HCM	heart:	n/a
48	chr1:173684007-173684057	HEEpiC	esophagus:	n/a
49	chr1:173683938-173683988	NHBE	bronchial:	n/a
50	chr1:173683890-173683940	U87	brain:	n/a

(count:45 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:173662464..173664753-chr1:173682895..173685625,2	K562	blood:
2	chr1:173688555..173690351-chr1:173791646..173794007,2	K562	blood:
3	chr1:173682439..173685635-chr1:173828531..173832401,4	MCF-7	breast:
4	chr1:173680351..173683002-chr1:173689911..173692365,2	K562	blood:
5	chr1:173670333..173674200-chr1:173680679..173684333,3	K562	blood:
6	chr1:173659508..173662067-chr1:173673058..173675830,2	K562	blood:
7	chr1:173669533..173671406-chr1:173836514..173838083,2	K562	blood:
8	chr1:173445598..173446579-chr1:173683742..173684289,2	Hela-S3	cervix:
9	chr1:173682535..173686916-chr1:173792397..173795534,7	K562	blood:
10	chr1:173680023..173685703-chr1:173685874..173692365,9	K562	blood:
11	chr1:173682967..173685869-chr1:173831317..173832954,2	K562	blood:
12	chr1:173686890..173689888-chr1:173826040..173828331,2	MCF-7	breast:
13	chr1:28974821..28975606-chr1:173683905..173684721,2	Hela-S3	cervix:
14	chr1:173686308..173688392-chr1:173689930..173692042,2	K562	blood:
15	chr1:173657950..173659742-chr1:173835067..173837158,2	K562	blood:
16	chr1:173675475..173677771-chr1:173680197..173682201,2	K562	blood:
17	chr1:173675475..173677771-chr1:173680197..173682201,2	K562	blood:
18	chr1:173684233..173685986-chr1:173834072..173838019,3	K562	blood:
19	chr1:173683067..173686676-chr1:173791976..173794755,4	K562	blood:
20	chr1:173445699..173447301-chr1:173673638..173675613,2	MCF-7	breast:
21	chr1:173679565..173681727-chr1:173834701..173836645,2	MCF-7	breast:
22	chr1:173686216..173687823-chr1:173831086..173833729,2	K562	blood:
23	chr1:173687895..173689585-chr1:173692482..173695234,2	MCF-7	breast:
24	chr1:173684233..173688038-chr1:173834072..173837696,4	K562	blood:
25	chr1:173674413..173677381-chr1:173682341..173684906,2	MCF-7	breast:
26	chr1:173680351..173683002-chr1:173689911..173692365,2	K562	blood:
27	chr1:173682123..173683698-chr1:173835708..173837673,2	K562	blood:
28	chr1:173656269..173659170-chr1:173662105..173664583,2	K562	blood:
29	chr1:173659508..173662067-chr1:173673058..173675830,2	K562	blood:
30	chr1:173648900..173651507-chr1:173681730..173683630,2	K562	blood:
31	chr1:173656269..173659170-chr1:173662105..173664583,2	K562	blood:
32	chr1:173400007..173400614-chr1:173658247..173658885,3	MCF-7	breast:
33	chr1:173685811..173687806-chr1:173687936..173689496,2	K562	blood:
34	chr1:173679457..173681127-chr1:173688388..173689983,2	MCF-7	breast:
35	chr1:173446233..173448381-chr1:173683311..173685708,2	MCF-7	breast:
36	chr1:173678046..173681772-chr1:173681873..173685345,5	K562	blood:
37	chr1:173679457..173681127-chr1:173688388..173689983,2	MCF-7	breast:
38	chr1:173682622..173685584-chr17:56707840..56709510,2	MCF-7	breast:
39	chr1:173685811..173687806-chr1:173687936..173689496,2	K562	blood:
40	chr1:173686308..173688392-chr1:173689930..173692042,2	K562	blood:
41	chr1:173682123..173683874-chr1:173835330..173837208,2	K562	blood:
42	chr1:173691682..173694241-chr1:173700147..173703100,2	K562	blood:
43	chr1:173684004..173686293-chr1:173689052..173693084,4	MCF-7	breast:
44	chr1:173602098..173604115-chr1:173674279..173675875,2	K562	blood:
45	chr1:173682287..173685888-chr1:173836010..173838228,4	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-KLHL20-2	chr1:173684080-173684217	NONHSAT007648
2	lnc-KLHL20-2	chr1:173684662-173684793	NONHSAT007648
3	lnc-KLHL20-2	chr1:173685142-173685205	NONHSAT007648

No data

Variant related genes	Relation type
KLHL20	TF binding region
KLHL20	CpG island
ENSG00000076321	chromatin interactions
ENSG00000117593	chromatin interactions
ENSG00000185278	chromatin interactions
ENSG00000120334	chromatin interactions
ENSG00000208317	chromatin interactions
ENSG00000234741	chromatin interactions
ENSG00000270084	chromatin interactions
ENSG00000117592	chromatin interactions
ENSG00000270103	chromatin interactions
ENSG00000212195	chromatin interactions

Extended variants
information (count: 980 )
Associated
traits (count: 91 )

Variant overlapped rSNPs/rCNVs (count:980 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs574079871	chr1:173653455-173653456	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs186472234	chr1:173653495-173653496	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs145593752	chr1:173653551-173653552	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs576547126	chr1:173653637-173653638	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs545641073	chr1:173653699-173653700	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs559505911	chr1:173653752-173653753	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs190513881	chr1:173653808-173653809	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs369020394	chr1:173653823-173653824	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs2126126	chr1:173653854-173653855	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs561994785	chr1:173653861-173653862	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs570701861	chr1:173653874-173653875	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs183118927	chr1:173653884-173653885	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs374897845	chr1:173653890-173653891	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs570922454	chr1:173653896-173653897	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs533476081	chr1:173653941-173653942	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs187621597	chr1:173653957-173653958	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs532545057	chr1:173654024-173654025	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs148458183	chr1:173654076-173654077	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs34795257	chr1:173654112-173654113	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs535704754	chr1:173654114-173654115	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs142612417	chr1:173654117-173654118	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs569232462	chr1:173654142-173654143	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs191132614	chr1:173654145-173654146	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs10158568	chr1:173654154-173654155	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs576485525	chr1:173654185-173654186	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs142046558	chr1:173654213-173654214	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs552835708	chr1:173654238-173654239	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs572974263	chr1:173654327-173654328	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs534962871	chr1:173654358-173654359	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs561934665	chr1:173654391-173654392	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs530840016	chr1:173654434-173654435	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs145835472	chr1:173654470-173654471	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs564474481	chr1:173654478-173654479	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs183444156	chr1:173654491-173654492	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs187431494	chr1:173654499-173654500	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs566880892	chr1:173654545-173654546	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs552529527	chr1:173654554-173654555	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs370628360	chr1:173654656-173654657	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs147776902	chr1:173654711-173654712	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs549181589	chr1:173654741-173654742	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs569169622	chr1:173654777-173654778	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs111229829	chr1:173654801-173654802	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs184569110	chr1:173654847-173654848	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs372224959	chr1:173654964-173654965	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs570421935	chr1:173655007-173655008	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs539094031	chr1:173655043-173655044	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs553429101	chr1:173655155-173655156	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs375323839	chr1:173655224-173655225	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs572872125	chr1:173655225-173655226	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs369567293	chr1:173655242-173655243	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:91)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Autism	22495311	CNVD
Hepatocellular carcinoma	16750200	CNVD
Liposarcoma	21253554	CNVD
Burkitt''s lymphoma	18698080	CNVD
Melanoma	18172304	CNVD
Cancer	21183584	CNVD
Multiple myeloma	16461302	CNVD
Rett syndrome	21593744	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Medulloblastoma	21979893	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
Non-small cell lung cancer	21829676	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Non-small cell lung cancer	21044232	CNVD
Cervical cancer	21063398	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	20632083	CNVD
Endometrial cancer	22040021	CNVD
Ewing''s sarcoma	21437220	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	21264507	CNVD
Multiple myeloma	21628407	CNVD
Cancer	16751803	CNVD
Prostate cancer	16705090	CNVD
Neuroblastoma	19435921	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16461572	CNVD
Intracranial tumor	16823260	CNVD
Medulloblastoma	18056178	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Neuroblastoma	21899760	CNVD
Bladder cancer	19088036	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17002787	CNVD
Breast cancer	21858162	CNVD
Retinoblastoma	19183342	CNVD
Non-small cell lung cancer	21385341	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Chordoma	18071362	CNVD
Hepatocellular carcinoma	18803288	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Urothelial carcinoma	21177765	CNVD
Burkitt''s lymphoma	19759907	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Testicular germ cell tumor	18059402	CNVD
Trisomy 5 syndrome	21098271	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Breast cancer	21611746	CNVD
Neuroblastoma	18923191	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ewing''s sarcoma	17952124	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Developmental delay	21147756	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	21509527	CNVD
Glioblastoma multiforme	17369134	CNVD
Cancer	17440070	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:738 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:173639000-173657200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr1:173645800-173654600	Weak transcription	H1 Cell Line	embryonic stem cell
3	chr1:173650000-173654600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr1:173651800-173657400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
5	chr1:173652400-173654800	Weak transcription	HUES64 Cell Line	embryonic stem cell
6	chr1:173652600-173654600	Weak transcription	HUES6 Cell Line	embryonic stem cell
7	chr1:173652600-173654600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
8	chr1:173652600-173654800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
9	chr1:173652800-173653800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
10	chr1:173652800-173656800	Weak transcription	HUES48 Cell Line	embryonic stem cell
11	chr1:173653000-173653600	Enhancers	Rectal Mucosa Donor 29	rectum
12	chr1:173653400-173654600	Weak transcription	K562	blood
13	chr1:173653800-173654000	Enhancers	iPS-15b Cell Line	embryonic stem cell
14	chr1:173654000-173654400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
15	chr1:173654400-173655200	Enhancers	iPS-15b Cell Line	embryonic stem cell
16	chr1:173654600-173655000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr1:173654600-173655000	Enhancers	iPS-18 Cell Line	embryonic stem cell
18	chr1:173654600-173655400	Enhancers	H1 Cell Line	embryonic stem cell
19	chr1:173654600-173655600	Enhancers	HUES6 Cell Line	embryonic stem cell
20	chr1:173654600-173655800	Enhancers	K562	blood
21	chr1:173654800-173655200	Enhancers	iPS-20b Cell Line	embryonic stem cell
22	chr1:173654800-173655800	Enhancers	HUES64 Cell Line	embryonic stem cell
23	chr1:173655000-173655800	Enhancers	Primary hematopoietic stem cells short term culture	blood
24	chr1:173655000-173656600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
25	chr1:173655200-173655600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
26	chr1:173655200-173656800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
27	chr1:173655600-173655800	Enhancers	iPS-15b Cell Line	embryonic stem cell
28	chr1:173655600-173656800	Weak transcription	HUES6 Cell Line	embryonic stem cell
29	chr1:173655800-173657000	Weak transcription	HUES64 Cell Line	embryonic stem cell
30	chr1:173655800-173657200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
31	chr1:173655800-173657400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
32	chr1:173655800-173657400	Weak transcription	K562	blood
33	chr1:173656600-173657000	Enhancers	iPS-18 Cell Line	embryonic stem cell
34	chr1:173656800-173657600	Enhancers	HUES48 Cell Line	embryonic stem cell
35	chr1:173656800-173657800	Enhancers	HUES6 Cell Line	embryonic stem cell
36	chr1:173656800-173658600	Enhancers	iPS-20b Cell Line	embryonic stem cell
37	chr1:173657000-173657400	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
38	chr1:173657000-173657600	Enhancers	HUES64 Cell Line	embryonic stem cell
39	chr1:173657200-173657400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
40	chr1:173657200-173659000	Enhancers	iPS-15b Cell Line	embryonic stem cell
41	chr1:173657400-173657600	Flanking Bivalent TSS/Enh	Breast Myoepithelial Primary Cells	Breast
42	chr1:173657400-173657800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
43	chr1:173657400-173658000	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
44	chr1:173657400-173658200	Enhancers	Primary hematopoietic stem cells short term culture	blood
45	chr1:173657400-173658200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
46	chr1:173657400-173658400	Enhancers	K562	blood
47	chr1:173657400-173659000	Enhancers	iPS-18 Cell Line	embryonic stem cell
48	chr1:173657600-173658000	Bivalent/Poised TSS	Breast Myoepithelial Primary Cells	Breast
49	chr1:173657800-173658800	Weak transcription	HUES6 Cell Line	embryonic stem cell
50	chr1:173658000-173658800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell

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