Variant report

Variant	nsv892157
Chromosome Location	chr9:6093790-6322415
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1889)
CpG islands
(count:183)
Chromatin interactive
region (count:34)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1889 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:6306047-6306247	HepG2	liver:	n/a	n/a
2	ARID3A	chr9:6197394-6197552	HepG2	liver:	n/a	n/a
3	ARID3A	chr9:6236398-6236588	HepG2	liver:	n/a	n/a
4	ARID3A	chr9:6236968-6237134	HepG2	liver:	n/a	n/a
5	ARID3A	chr9:6272234-6272566	HepG2	liver:	n/a	n/a
6	ARID3A	chr9:6238753-6239428	HepG2	liver:	n/a	n/a
7	ATF1	chr9:6106923-6107351	K562	blood:	n/a	n/a
8	ATF2	chr9:6197314-6197660	H1-hESC	embryonic stem cell:	n/a	n/a
9	ATF2	chr9:6184965-6185468	GM12878	blood:	n/a	n/a
10	ATF2	chr9:6184846-6185494	GM12878	blood:	n/a	n/a
11	BACH1	chr9:6212812-6213039	K562	blood:	n/a	n/a
12	BATF	chr9:6243750-6244097	GM12878	blood:	n/a	chr9:6243981-6243992
13	BATF	chr9:6184773-6185635	GM12878	blood:	n/a	n/a
14	BATF	chr9:6133370-6133661	GM12878	blood:	n/a	n/a
15	BATF	chr9:6243774-6244147	GM12878	blood:	n/a	chr9:6243981-6243992
16	BATF	chr9:6096712-6097082	GM12878	blood:	n/a	n/a
17	BATF	chr9:6185007-6185418	GM12878	blood:	n/a	n/a
18	BATF	chr9:6186725-6187026	GM12878	blood:	n/a	n/a
19	BCL11A	chr9:6185090-6185360	GM12878	blood:	n/a	n/a
20	BCL11A	chr9:6185001-6185445	GM12878	blood:	n/a	n/a
21	BCL11A	chr9:6133721-6133994	GM12878	blood:	n/a	n/a
22	BCL11A	chr9:6243799-6244059	GM12878	blood:	n/a	n/a
23	BCLAF1	chr9:6184828-6185523	GM12878	blood:	n/a	n/a
24	BHLHE40	chr9:6306060-6306216	GM12878	blood:	n/a	n/a
25	BHLHE40	chr9:6243865-6244064	GM12878	blood:	n/a	n/a
26	BHLHE40	chr9:6238901-6239586	HepG2	liver:	n/a	n/a
27	BRCA1	chr9:6152733-6153851	Hela-S3	cervix:	n/a	n/a
28	BRCA1	chr9:6305856-6306260	Hela-S3	cervix:	n/a	n/a
29	BRCA1	chr9:6218063-6218503	Hela-S3	cervix:	n/a	n/a
30	BRCA1	chr9:6107086-6107152	GM12878	blood:	n/a	n/a
31	BRCA1	chr9:6102464-6102968	Hela-S3	cervix:	n/a	n/a
32	BRCA1	chr9:6238263-6238286	Hela-S3	cervix:	n/a	n/a
33	BRCA1	chr9:6215680-6215690	Hela-S3	cervix:	n/a	n/a
34	CBX3	chr9:6173885-6174320	HCT-116	colon:	n/a	n/a
35	CBX3	chr9:6102440-6102981	HCT-116	colon:	n/a	n/a
36	CBX3	chr9:6173999-6174182	K562	blood:	n/a	n/a
37	CBX3	chr9:6102461-6102997	HCT-116	colon:	n/a	n/a
38	CBX3	chr9:6106866-6107334	K562	blood:	n/a	n/a
39	CBX3	chr9:6106944-6107559	HCT-116	colon:	n/a	n/a
40	CBX3	chr9:6173953-6174243	K562	blood:	n/a	n/a
41	CEBPB	chr9:6163515-6163840	HepG2	liver:	n/a	chr9:6163675-6163686
42	CEBPB	chr9:6217956-6218616	Hela-S3	cervix:	n/a	n/a
43	CEBPB	chr9:6102238-6103068	Hela-S3	cervix:	n/a	n/a
44	CEBPB	chr9:6272319-6272559	H1-hESC	embryonic stem cell:	n/a	chr9:6272425-6272434 chr9:6272425-6272434 chr9:6272425-6272434 chr9:6272423-6272434 chr9:6272424-6272435 chr9:6272425-6272434 chr9:6272423-6272436
45	CEBPB	chr9:6218092-6218568	ECC-1	luminal epithelium:	n/a	n/a
46	CEBPB	chr9:6096745-6097070	IMR90	lung:	n/a	n/a
47	CEBPB	chr9:6133720-6134050	Hela-S3	cervix:	n/a	chr9:6133912-6133923 chr9:6133750-6133761
48	CEBPB	chr9:6277386-6277817	ECC-1	luminal epithelium:	n/a	chr9:6277616-6277627
49	CEBPB	chr9:6277442-6277805	HepG2	liver:	n/a	chr9:6277616-6277627
50	CEBPB	chr9:6107120-6107418	H1-hESC	embryonic stem cell:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:6109415-6109465	AG09309	skin:	n/a
2	chr9:6109415-6109465	HAEpiC	amniotic membrane:	n/a
3	chr9:6252007-6252057	HPAEpiC	pulmonary alveolar:	n/a
4	chr9:6109415-6109465	K562	blood:	n/a
5	chr9:6241371-6241421	PrEC	prostate:	n/a
6	chr9:6252007-6252057	PANC-1	pancreas:	n/a
7	chr9:6109415-6109465	HRCEpiC	kidney:	n/a
8	chr9:6241371-6241421	BE2_C	brain:	n/a
9	chr9:6252007-6252057	HCT-116	colon:	n/a
10	chr9:6241371-6241421	AG10803	skin:	n/a
11	chr9:6241371-6241421	CMK	blood:	n/a
12	chr9:6252007-6252057	LNCaP	prostate:	n/a
13	chr9:6109415-6109465	RPTEC	kidney:	n/a
14	chr9:6252007-6252057	MCF10A-Er-Src	breast:	n/a
15	chr9:6109415-6109465	MCF-7	breast:	n/a
16	chr9:6252007-6252057	BE2_C	brain:	n/a
17	chr9:6252007-6252057	GM19239	blood:	n/a
18	chr9:6252007-6252057	SAEC	small airway:	n/a
19	chr9:6241371-6241421	PFSK-1	brain:	n/a
20	chr9:6241371-6241421	HUVEC	blood vessel:	n/a
21	chr9:6109415-6109465	HEK293	kidney:	embryo
22	chr9:6109415-6109465	Caco-2	colon:	n/a
23	chr9:6252007-6252057	Hepatocyte	liver:	n/a
24	chr9:6252007-6252057	SKMC	muscle:	n/a
25	chr9:6252007-6252057	AG09309	skin:	n/a
26	chr9:6252007-6252057	HNPCEpiC	eye:	n/a
27	chr9:6109415-6109465	SK-N-MC	brain:	n/a
28	chr9:6241371-6241421	HCF	heart:	n/a
29	chr9:6241371-6241421	Hela-S3	cervix:	n/a
30	chr9:6241371-6241421	AG09319	gingival:	n/a
31	chr9:6109415-6109465	HRE	kidney:	n/a
32	chr9:6252007-6252057	SK-N-SH	brain:	n/a
33	chr9:6109415-6109465	CMK	blood:	n/a
34	chr9:6241371-6241421	Jurkat	blood:	n/a
35	chr9:6252007-6252057	SK-N-MC	brain:	n/a
36	chr9:6241371-6241421	HCPEpiC	choroid plexus:	n/a
37	chr9:6241371-6241421	GM12878	blood:	n/a
38	chr9:6252007-6252057	Caco-2	colon:	n/a
39	chr9:6241371-6241421	NHBE	bronchial:	n/a
40	chr9:6252007-6252057	RPTEC	kidney:	n/a
41	chr9:6252007-6252057	NT2-D1	testis:	n/a
42	chr9:6109415-6109465	AG04450	lung:	fetal
43	chr9:6241371-6241421	ProgFib	skin:	n/a
44	chr9:6252007-6252057	HL-60	blood:	n/a
45	chr9:6252007-6252057	SK-N-SH_RA	brain:	n/a
46	chr9:6109415-6109465	GM06990	blood:	n/a
47	chr9:6241371-6241421	IMR90	lung:	fetal
48	chr9:6241371-6241421	SAEC	small airway:	n/a
49	chr9:6252007-6252057	U87	brain:	n/a
50	chr9:6109415-6109465	HMEC	breast:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr9:6055397..6056252-chr9:6305741..6306569,2	K562	blood:
2	chr9:6163367..6165821-chr9:6169712..6171511,2	K562	blood:
3	chr9:6244528..6246233-chr9:6251156..6253683,2	MCF-7	breast:
4	chr9:6307810..6309784-chr9:6311496..6314006,2	K562	blood:
5	chr9:6194592..6195131-chr9:6305762..6306590,2	MCF-7	breast:
6	chr9:6234179..6236096-chr9:6238826..6241061,2	K562	blood:
7	chr9:6107045..6110016-chr9:6112328..6114714,2	K562	blood:
8	chr9:6163920..6166108-chr9:6170937..6173147,2	MCF-7	breast:
9	chr9:6163920..6166108-chr9:6170937..6173147,2	MCF-7	breast:
10	chr9:6174199..6177048-chr9:6181572..6183383,2	MCF-7	breast:
11	chr9:6163094..6165877-chr9:6167250..6170974,4	K562	blood:
12	chr9:6182316..6185009-chr9:6186082..6187902,2	K562	blood:
13	chr13:43706108..43706705-chr9:6170816..6171542,2	MCF-7	breast:
14	chr9:6244528..6246233-chr9:6251156..6253683,2	MCF-7	breast:
15	chr9:6196840..6197620-chr9:6306018..6306519,2	MCF-7	breast:
16	chr9:6305170..6307719-chr9:6307772..6310215,2	K562	blood:
17	chr9:6163094..6165877-chr9:6167250..6170974,4	K562	blood:
18	chr9:6149075..6150608-chr9:6166608..6168151,2	MCF-7	breast:
19	chr9:6266181..6268457-chr9:6269163..6272196,3	K562	blood:
20	chr9:6149075..6150608-chr9:6166608..6168151,2	MCF-7	breast:
21	chr9:6307810..6309784-chr9:6311496..6314006,2	K562	blood:
22	chr9:6195102..6195794-chr9:6568308..6568912,2	K562	blood:
23	chr9:6201029..6203540-chr9:6215680..6218483,2	K562	blood:
24	chr9:6163367..6165821-chr9:6169712..6171511,2	K562	blood:
25	chr9:6054654..6056123-chr9:6305613..6307254,7	MCF-7	breast:
26	chr9:6182316..6185009-chr9:6186082..6187902,2	K562	blood:
27	chr9:6107045..6110016-chr9:6112328..6114714,2	K562	blood:
28	chr9:6241308..6243910-chr9:6245192..6247268,2	MCF-7	breast:
29	chr9:6174199..6177048-chr9:6181572..6183383,2	MCF-7	breast:
30	chr9:6234179..6236096-chr9:6238826..6241061,2	K562	blood:
31	chr9:6196840..6197620-chr9:6306018..6306519,2	MCF-7	breast:
32	chr9:6305170..6307719-chr9:6307772..6310215,2	K562	blood:
33	chr9:6266181..6268457-chr9:6269163..6272196,3	K562	blood:
34	chr9:6194592..6195131-chr9:6305762..6306590,2	MCF-7	breast:

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TPD52L3-1	chr9:6242192-6242734	NONHSAT130126
2	lnc-IL33-2	chr9:6197158-6197248	NONHSAT130125
3	lnc-IL33-1	chr9:6276640-6276974	NONHSAT130127
4	lnc-IL33-2	chr9:6195934-6196846	NONHSAT130125
5	lnc-TPD52L3-1	chr9:6241693-6241785	NONHSAT130126

No data

Variant related genes	Relation type
ENSG00000237274	TF binding region
IL33	TF binding region
ENSG00000233846	TF binding region
ENSG00000228132	TF binding region
ENSG00000237274	CpG island
IL33	CpG island
ENSG00000233846	CpG island
ENSG00000228132	CpG island
ENSG00000237158	chromatin interactions
ENSG00000137033	chromatin interactions

Extended variants
information (count: 7834 )
Associated
traits (count: 109 )

Variant overlapped rSNPs/rCNVs (count:7834 , 50 per page) page: 1 2 3 4 5 6 7 ... 157

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs425489	chr9:6093790-6093791	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs543511298	chr9:6093812-6093813	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs555426889	chr9:6093813-6093814	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs186290012	chr9:6093923-6093924	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs191060711	chr9:6093955-6093956	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs2150969	chr9:6093990-6093991	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs116351633	chr9:6093996-6093997	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs148914539	chr9:6094004-6094005	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs56260335	chr9:6094043-6094044	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs545166471	chr9:6094091-6094092	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs563665909	chr9:6094134-6094135	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs181480436	chr9:6094141-6094142	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs549019707	chr9:6094156-6094157	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs186845950	chr9:6094172-6094173	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs528457624	chr9:6094185-6094186	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs547022966	chr9:6094238-6094239	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs571886492	chr9:6094302-6094303	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs368447599	chr9:6094339-6094340	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs557543354	chr9:6094353-6094354	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs372425141	chr9:6094376-6094377	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs192002860	chr9:6094390-6094391	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs537148983	chr9:6094400-6094401	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs376973964	chr9:6094427-6094428	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs399834	chr9:6094454-6094455	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs390158	chr9:6094463-6094464	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs182934350	chr9:6094471-6094472	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs532942203	chr9:6094493-6094494	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs188439674	chr9:6094499-6094500	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs544946222	chr9:6094501-6094502	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs563145857	chr9:6094522-6094523	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs189710573	chr9:6094569-6094570	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs375031988	chr9:6094575-6094576	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs116934118	chr9:6094597-6094598	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs561042049	chr9:6094615-6094616	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs528492710	chr9:6094620-6094621	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs142246448	chr9:6094648-6094649	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs114742536	chr9:6094658-6094659	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs182215980	chr9:6094662-6094663	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs372418346	chr9:6094690-6094691	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs550949006	chr9:6094721-6094722	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs376451083	chr9:6094730-6094731	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs146792843	chr9:6094749-6094750	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs1576463	chr9:6094755-6094756	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs114131009	chr9:6094756-6094757	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs534355364	chr9:6094758-6094759	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs371893174	chr9:6094762-6094763	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs140588869	chr9:6094852-6094853	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs577519709	chr9:6094864-6094865	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs538934031	chr9:6095007-6095008	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs556827258	chr9:6095025-6095026	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:109)

Disease	PMID	Source
Chronic lymphocytic leukemia	21546498	CNVD
Intracranial aneurysm	16715129	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Disorders of sex development	22290220	CNVD
Glioblastoma multiforme	21080181	CNVD
Sudden cardiac death	19188705	CNVD
Non-small cell lung cancer	21829676	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	21183584	CNVD
Non-small cell lung cancer	21952639	CNVD
Disorders of sex development	21048976	CNVD
Neuroblastoma	18923191	CNVD
Intellectual disability	22102821	CNVD
abnormal development	18461090	CNVD
Honadal dysgenesis	21048976	CNVD
Medulloblastoma	21979893	CNVD
Lung cancer	16740712	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Breast cancer	16608533	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	16272173	CNVD
Hepatocellular carcinoma	16750200	CNVD
Breast cancer	17133270	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Cervical cancer	21063398	CNVD
Retinoblastoma	22278416	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Melanoma	18172304	CNVD
Biliary cancer	19435499	CNVD
Gastric cancer	21586687	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Myopathy	18421352	CNVD
Neuroblastoma	18664255	CNVD
Acute lymphoblastic leukemia	18957548	CNVD
Myeloproliferative neoplasm	17564968	CNVD
Malignant meningioma	17937814	CNVD
Glioma	21971842	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	17603634	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Oligodendroglial tumors	17285580	CNVD
Cutaneous squamous cell carcinomas	19131950	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Chordoma	18071362	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chordoma	21602918	CNVD
Renal cell carcinoma	18592004	CNVD
Developmental delay	19490664	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
microdeletion syndrome	16199537	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Cancer	20164919	CNVD
Chronic myeloid leukemia	21384125	CNVD
Ovarian cancer	21720365	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
small cell lung cancer	20016488	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Developmental delay	21147756	CNVD
Lung cancer	18438408	CNVD
XY gonadal dysgenesis	20685758	CNVD
Urothelial carcinoma	21177765	CNVD
Oral cancer	21386901	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Myelodysplastic syndrome	21251322	CNVD
Breast cancer	21785460	CNVD
Prostate cancer	18632612	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21364760	CNVD
Breast cancer	21858162	CNVD
Renal cell carcinoma	21668985	CNVD
Autism	22495311	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Myelofibrosis	22110671	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Hepatocellular carcinoma	18803288	CNVD
Metastatic melanoma	18483359	CNVD
Glioblastoma	19074898	CNVD
Malignant melanoma	19074898	CNVD
Prostate cancer	16573809	CNVD
Metanephric adenoma	20802469	CNVD
Medulloblastoma	16783165	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD
Autism	20858261	CNVD
Epilepsy	20858261	CNVD
Mental retardation	20858261	CNVD
Schizophrenia	23813976	CNVD
Melanoma	20877625	CNVD
T-cell lymphomas	22341440	CNVD
Renal cell carcinoma	21215367	CNVD
Cancer	21215367	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:1153 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:6087800-6097200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr9:6091000-6098200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
3	chr9:6091200-6096400	Weak transcription	NHEK	skin
4	chr9:6091200-6096600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
5	chr9:6091200-6096600	Weak transcription	NHDF-Ad	bronchial
6	chr9:6091800-6096400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr9:6096400-6099400	Enhancers	NHEK	skin
8	chr9:6096400-6100000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
9	chr9:6096400-6100200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
10	chr9:6096400-6100200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
11	chr9:6096400-6100400	Enhancers	HMEC	breast
12	chr9:6096600-6097600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
13	chr9:6096600-6099000	Enhancers	Osteobl	bone
14	chr9:6096600-6099200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
15	chr9:6096600-6099200	Enhancers	NHDF-Ad	bronchial
16	chr9:6096600-6100200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
17	chr9:6096800-6098400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
18	chr9:6097200-6098400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
19	chr9:6097400-6097600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
20	chr9:6097600-6098000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
21	chr9:6098000-6098800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
22	chr9:6098000-6099200	Enhancers	HUVEC	blood vessel
23	chr9:6098200-6098400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
24	chr9:6098200-6098800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
25	chr9:6098200-6098800	Enhancers	Hela-S3	cervix
26	chr9:6098400-6101800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
27	chr9:6098400-6102400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
28	chr9:6098800-6099000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr9:6098800-6101000	Weak transcription	Hela-S3	cervix
30	chr9:6098800-6101800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
31	chr9:6098800-6105200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
32	chr9:6099000-6100200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
33	chr9:6099200-6101800	Weak transcription	NHDF-Ad	bronchial
34	chr9:6099200-6102200	Weak transcription	HUVEC	blood vessel
35	chr9:6099200-6106600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
36	chr9:6099400-6101600	Weak transcription	NHEK	skin
37	chr9:6099600-6100200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
38	chr9:6100000-6101600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
39	chr9:6100200-6100400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
40	chr9:6100200-6101600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
41	chr9:6100200-6102000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
42	chr9:6100400-6101600	Weak transcription	HMEC	breast
43	chr9:6101000-6102000	Enhancers	Hela-S3	cervix
44	chr9:6101600-6103400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
45	chr9:6101600-6104800	Enhancers	NHEK	skin
46	chr9:6101600-6105400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
47	chr9:6101600-6107200	Enhancers	HMEC	breast
48	chr9:6101800-6103200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
49	chr9:6101800-6103400	Enhancers	NHDF-Ad	bronchial
50	chr9:6101800-6105400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin

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