Variant report

Variant	nsv895885
Chromosome Location	chr10:91912493-91988922
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr10:91927400-91927804	GM12878	blood:	n/a	n/a
2	ATF2	chr10:91927258-91927862	GM12878	blood:	n/a	n/a
3	ATF3	chr10:91939363-91939912	HCT-116	colon:	n/a	n/a
4	ATF3	chr10:91986779-91987513	HCT-116	colon:	n/a	n/a
5	ATF3	chr10:91982032-91982513	HCT-116	colon:	n/a	n/a
6	ATF3	chr10:91986749-91987509	HCT-116	colon:	n/a	n/a
7	BATF	chr10:91927387-91927750	GM12878	blood:	n/a	n/a
8	BATF	chr10:91986969-91987320	GM12878	blood:	n/a	chr10:91987115-91987126 chr10:91987112-91987122 chr10:91987116-91987126
9	BATF	chr10:91927485-91927777	GM12878	blood:	n/a	n/a
10	BATF	chr10:91959364-91959521	GM12878	blood:	n/a	n/a
11	BCL11A	chr10:91927479-91927794	GM12878	blood:	n/a	n/a
12	BCL3	chr10:91927465-91927749	GM12878	blood:	n/a	n/a
13	BHLHE40	chr10:91927540-91927714	GM12878	blood:	n/a	n/a
14	CBX3	chr10:91986069-91988019	HCT-116	colon:	n/a	n/a
15	CBX3	chr10:91981946-91983153	HCT-116	colon:	n/a	n/a
16	CBX3	chr10:91939280-91939970	HCT-116	colon:	n/a	n/a
17	CBX3	chr10:91986546-91987624	HCT-116	colon:	n/a	n/a
18	CEBPB	chr10:91921590-91921855	H1-hESC	embryonic stem cell:	n/a	chr10:91921727-91921738 chr10:91921728-91921739
19	CEBPB	chr10:91982877-91983026	H1-hESC	embryonic stem cell:	n/a	n/a
20	CEBPB	chr10:91927610-91927719	HepG2	liver:	n/a	n/a
21	CEBPB	chr10:91927487-91927750	Hela-S3	cervix:	n/a	chr10:91927539-91927550
22	CEBPB	chr10:91939318-91939779	A549	lung:	n/a	chr10:91939553-91939564 chr10:91939555-91939564 chr10:91939553-91939566 chr10:91939555-91939566
23	CEBPB	chr10:91939218-91940011	HCT-116	colon:	n/a	chr10:91939553-91939564 chr10:91939555-91939564 chr10:91939553-91939566 chr10:91939555-91939566
24	CEBPB	chr10:91939168-91940050	HCT-116	colon:	n/a	chr10:91939553-91939564 chr10:91939555-91939564 chr10:91939553-91939566 chr10:91939555-91939566
25	CEBPB	chr10:91986626-91987710	HCT-116	colon:	n/a	n/a
26	CEBPB	chr10:91974081-91974359	A549	lung:	n/a	chr10:91974208-91974219
27	CEBPB	chr10:91974080-91974375	HepG2	liver:	n/a	chr10:91974208-91974219
28	CEBPB	chr10:91986728-91987599	HCT-116	colon:	n/a	n/a
29	CEBPB	chr10:91927401-91927883	HCT-116	colon:	n/a	chr10:91927539-91927550
30	CEBPB	chr10:91939385-91939711	HepG2	liver:	n/a	chr10:91939553-91939564 chr10:91939555-91939564 chr10:91939553-91939566 chr10:91939555-91939566
31	CEBPB	chr10:91921659-91921850	HepG2	liver:	n/a	chr10:91921727-91921738 chr10:91921728-91921739
32	CEBPB	chr10:91939310-91939832	MCF-7	breast:	n/a	chr10:91939553-91939564 chr10:91939555-91939564 chr10:91939553-91939566 chr10:91939555-91939566
33	CEBPB	chr10:91981941-91983205	HCT-116	colon:	n/a	n/a
34	CEBPB	chr10:91939266-91939861	MCF-7	breast:	n/a	chr10:91939553-91939564 chr10:91939555-91939564 chr10:91939553-91939566 chr10:91939555-91939566
35	CEBPB	chr10:91927556-91927750	IMR90	lung:	n/a	n/a
36	CEBPB	chr10:91939379-91939847	Hela-S3	cervix:	n/a	chr10:91939553-91939564 chr10:91939555-91939564 chr10:91939553-91939566 chr10:91939555-91939566
37	CEBPB	chr10:91974066-91974336	IMR90	lung:	n/a	chr10:91974208-91974219
38	CEBPB	chr10:91939390-91939807	IMR90	lung:	n/a	chr10:91939553-91939564 chr10:91939555-91939564 chr10:91939553-91939566 chr10:91939555-91939566
39	CEBPB	chr10:91974118-91974318	K562	blood:	n/a	chr10:91974208-91974219
40	CEBPB	chr10:91939420-91939777	A549	lung:	n/a	chr10:91939553-91939564 chr10:91939555-91939564 chr10:91939553-91939566 chr10:91939555-91939566
41	CEBPB	chr10:91985129-91985337	A549	lung:	n/a	chr10:91985234-91985247 chr10:91985267-91985278 chr10:91985265-91985276
42	CEBPB	chr10:91985119-91985339	HepG2	liver:	n/a	chr10:91985234-91985247 chr10:91985267-91985278 chr10:91985265-91985276
43	CHD2	chr10:91933751-91933782	GM12878	blood:	n/a	n/a
44	CREB1	chr10:91957566-91957939	GM12878	blood:	n/a	n/a
45	CTCF	chr10:91988900-91989050	AoAF	blood vessel:	n/a	n/a
46	CTCF	chr10:91977080-91977230	HCFaa	heart:	n/a	n/a
47	CTCF	chr10:91943384-91943420	GM13976	blood:	n/a	n/a
48	CTCF	chr10:91982851-91983018	NHEK	skin:	n/a	n/a
49	CTCF	chr10:91963320-91963470	HUVEC	blood vessel:	n/a	n/a
50	CTCF	chr10:91918793-91918842	Pancreas_OC	pancreas:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:91919031-91919081	NT2-D1	testis:	n/a
2	chr10:91919031-91919081	A549	lung:	n/a
3	chr10:91919031-91919081	AG09309	skin:	n/a
4	chr10:91919031-91919081	LNCaP	prostate:	n/a
5	chr10:91919031-91919081	Hepatocyte	liver:	n/a
6	chr10:91919031-91919081	GM06990	blood:	n/a
7	chr10:91919031-91919081	HAEpiC	amniotic membrane:	n/a
8	chr10:91919031-91919081	Jurkat	blood:	n/a
9	chr10:91919031-91919081	HEK293	kidney:	embryo
10	chr10:91919031-91919081	HRE	kidney:	n/a
11	chr10:91919031-91919081	BE2_C	brain:	n/a
12	chr10:91919031-91919081	CMK	blood:	n/a
13	chr10:91919031-91919081	NHDF-neo	bronchial:	n/a
14	chr10:91919031-91919081	MCF-7	breast:	n/a
15	chr10:91919031-91919081	AG04450	lung:	fetal
16	chr10:91919031-91919081	SK-N-SH	brain:	n/a
17	chr10:91919031-91919081	HRCEpiC	kidney:	n/a
18	chr10:91919031-91919081	GM12891	blood:	n/a
19	chr10:91919031-91919081	HepG2	liver:	n/a
20	chr10:91919031-91919081	HCT-116	colon:	n/a
21	chr10:91919031-91919081	ProgFib	skin:	n/a
22	chr10:91919031-91919081	HL-60	blood:	n/a
23	chr10:91919031-91919081	AG10803	skin:	n/a
24	chr10:91919031-91919081	Caco-2	colon:	n/a
25	chr10:91919031-91919081	HPAEpiC	pulmonary alveolar:	n/a
26	chr10:91919031-91919081	Hela-S3	cervix:	n/a
27	chr10:91919031-91919081	SKMC	muscle:	n/a
28	chr10:91919031-91919081	PFSK-1	brain:	n/a
29	chr10:91919031-91919081	HMEC	breast:	n/a
30	chr10:91919031-91919081	BJ	skin:	n/a
31	chr10:91919031-91919081	HNPCEpiC	eye:	n/a
32	chr10:91919031-91919081	HRPEpiC	eye:	n/a
33	chr10:91919031-91919081	GM19239	blood:	n/a
34	chr10:91919031-91919081	HCM	heart:	n/a
35	chr10:91919031-91919081	AoSMC	blood vessel:	n/a
36	chr10:91919031-91919081	K562	blood:	n/a
37	chr10:91919031-91919081	HCPEpiC	choroid plexus:	n/a
38	chr10:91919031-91919081	AG04449	skin:	fetal
39	chr10:91919031-91919081	NB4	blood:	n/a
40	chr10:91919031-91919081	AG09319	gingival:	n/a
41	chr10:91919031-91919081	H1-hESC	embryonic stem cell:	embryo
42	chr10:91919031-91919081	NHBE	bronchial:	n/a
43	chr10:91919031-91919081	ECC-1	luminal epithelium:	n/a
44	chr10:91919031-91919081	SK-N-MC	brain:	n/a
45	chr10:91919031-91919081	RPTEC	kidney:	n/a
46	chr10:91919031-91919081	HCF	heart:	n/a
47	chr10:91919031-91919081	HUVEC	blood vessel:	n/a
48	chr10:91919031-91919081	MCF10A-Er-Src	breast:	n/a
49	chr10:91919031-91919081	SAEC	small airway:	n/a
50	chr10:91919031-91919081	NH-A	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr10:91931353..91933621-chr10:91948075..91950614,2	K562	blood:
2	chr10:91967172..91968882-chr10:91972156..91974992,2	MCF-7	breast:
3	chr10:91967172..91968882-chr10:91972156..91974992,2	MCF-7	breast:
4	chr10:91931353..91933621-chr10:91948075..91950614,2	K562	blood:
5	chr10:91964674..91966722-chr10:91976037..91978433,2	MCF-7	breast:
6	chr10:91938353..91941143-chr10:91951885..91953423,2	MCF-7	breast:
7	chr10:91938353..91941143-chr10:91951885..91953423,2	MCF-7	breast:
8	chr10:91968000..91970356-chr10:91975660..91978114,2	MCF-7	breast:
9	chr10:91964674..91966722-chr10:91976037..91978433,2	MCF-7	breast:
10	chr10:91679148..91682138-chr10:91965404..91969772,3	MCF-7	breast:
11	chr10:91982612..91984620-chr10:91985971..91988082,2	MCF-7	breast:
12	chr10:91968000..91970356-chr10:91975660..91978114,2	MCF-7	breast:
13	chr10:91982612..91984620-chr10:91985971..91988082,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-KIF20B-8	chr10:91939472-91939926	NONHSAT015584
2	lnc-KIF20B-5	chr10:91923670-91923893	XLOC_008555
3	lnc-KIF20B-5	chr10:91965517-91965545	XLOC_008555
4	lnc-PANK1-8	chr10:91923408-91923717	NONHSAT015582
5	lnc-KIF20B-8	chr10:91924526-91924552	NONHSAT015584

Variant related genes	Relation type
RN7SKP143	TF binding region
RN7SKP143	CpG island

Extended variants
information (count: 3081 )
Associated
traits (count: 87 )

Variant overlapped rSNPs/rCNVs (count:3081 , 50 per page) page: 1 2 3 4 5 6 7 ... 62

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1329154	chr10:91912493-91912494	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs369137710	chr10:91912499-91912500	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs568649249	chr10:91912508-91912509	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs537202788	chr10:91912516-91912517	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs150480793	chr10:91912519-91912520	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs376794733	chr10:91912522-91912523	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs577605307	chr10:91912599-91912600	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs188225819	chr10:91912610-91912611	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs111571246	chr10:91912638-91912639	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs79949027	chr10:91912688-91912689	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs75999127	chr10:91912697-91912698	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs7904174	chr10:91912735-91912736	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs537287611	chr10:91912741-91912742	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs574575484	chr10:91912870-91912871	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs543249489	chr10:91912886-91912887	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs563639331	chr10:91912910-91912911	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs532257545	chr10:91912917-91912918	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs545820013	chr10:91912931-91912932	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs80056017	chr10:91912935-91912936	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs138509322	chr10:91912957-91912958	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs377056881	chr10:91912972-91912973	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs78515500	chr10:91912974-91912975	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs531179228	chr10:91913008-91913009	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs550881516	chr10:91913028-91913029	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs112046927	chr10:91913040-91913041	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs540160602	chr10:91913054-91913055	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs537021619	chr10:91913055-91913056	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs556425157	chr10:91913057-91913058	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs565685805	chr10:91913099-91913100	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs4933560	chr10:91913119-91913120	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs72822718	chr10:91913124-91913125	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs559055698	chr10:91913143-91913144	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs113649835	chr10:91913150-91913151	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs368620949	chr10:91913151-91913152	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs553764304	chr10:91913171-91913172	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs543636297	chr10:91913181-91913182	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs187372260	chr10:91913199-91913200	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs147899086	chr10:91913206-91913207	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs576594720	chr10:91913214-91913215	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs545702887	chr10:91913271-91913272	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs559176783	chr10:91913279-91913280	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs528533030	chr10:91913297-91913298	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs190141797	chr10:91913304-91913305	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs562246629	chr10:91913315-91913316	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs541114715	chr10:91913412-91913413	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs551026320	chr10:91913477-91913478	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs571070428	chr10:91913487-91913488	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs533522321	chr10:91913503-91913504	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs181628996	chr10:91913511-91913512	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs145266800	chr10:91913519-91913520	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:87)

Disease	PMID	Source
Gastric cancer	17908304	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Melanoma	18172304	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Ewing''s sarcoma	17952124	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	20724749	CNVD
Autism	22495311	CNVD
Prostate cancer	18632612	CNVD
Cockayne syndrome	18421352	CNVD
Glioblastoma	16823260	CNVD
Medulloblastoma	16968546	CNVD
Neuroblastoma	17533364	CNVD
Squamous cell cancer	21044232	CNVD
Glioma	21971842	CNVD
Cancer	21637783	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Lung cancer	18438408	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Usher syndrome	20538994	CNVD
Medulloblastoma	16783165	CNVD
Breast cancer	21785460	CNVD
Acute myeloid leukemia	20729466	CNVD
Prostate cancer	16573809	CNVD
Paraganglioma	17535989	CNVD
Submicroscopic aberration syndrome	21292638	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Pulmonary chondroma	17535989	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Colorectal cancer	18645599	CNVD
Polyposis syndrome	18645599	CNVD
Prostate cancer	17245344	CNVD
Glioblastoma multiforme	17369134	CNVD
Glioblastoma multiforme	21750150	CNVD
Breast cancer	22032731	CNVD
Ovarian cancer	20844748	CNVD
Glioblastoma multiforme	17002787	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	17603634	CNVD
Glioblastoma multiforme	17387387	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Breast cancer	21364760	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Wilms tumour	21544195	CNVD
small cell lung cancer	20016488	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Urothelial carcinoma	21177765	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Colorectal cancer	19359472	CNVD
Neurocytoma	17123091	CNVD
Prostate cancer	16461572	CNVD
Basal-like breast cancer	18066063	CNVD
Effusion lymphoma	18079361	CNVD
Lung cancer	21911935	CNVD
Myelofibrosis	22110671	CNVD
Prostate cancer	21088497	CNVD
Breast cancer	22048815	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Glioblastoma multiforme	22291905	CNVD
Glioblastoma multiforme	19435819	CNVD
Glioblastoma multiforme	22286061	CNVD
Intracranial ependymoma	16609018	CNVD
Breast cancer	16397240	CNVD
Chronic lymphocytic leukemia	21049055	CNVD
Cervical cancer	21062161	CNVD
Non-small cell lung cancer	21829676	CNVD
Melanoma	24453001	CNVD
Breast cancer	16608533	CNVD
Sezary syndrome	18413736	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:265 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:91910400-91927200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr10:91920600-91922000	Enhancers	NHDF-Ad	bronchial
3	chr10:91920600-91923200	Enhancers	NHLF	lung
4	chr10:91921000-91921200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
5	chr10:91921000-91922200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
6	chr10:91921200-91922000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
7	chr10:91921600-91921800	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
8	chr10:91921600-91922200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
9	chr10:91921600-91923000	Enhancers	Osteobl	bone
10	chr10:91922000-91922400	Weak transcription	NHDF-Ad	bronchial
11	chr10:91922000-91922800	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
12	chr10:91922200-91922600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
13	chr10:91922200-91923200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
14	chr10:91922400-91924000	Enhancers	NHDF-Ad	bronchial
15	chr10:91922400-91927000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
16	chr10:91922600-91923800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
17	chr10:91922800-91923000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
18	chr10:91923000-91927000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
19	chr10:91923000-91927000	Weak transcription	Osteobl	bone
20	chr10:91923200-91923800	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
21	chr10:91923200-91923800	Weak transcription	NHLF	lung
22	chr10:91923400-91923800	Enhancers	Esophagus	oesophagus
23	chr10:91923600-91923800	ZNF genes & repeats	Pancreas	Pancrea
24	chr10:91923800-91924400	Enhancers	HMEC	breast
25	chr10:91923800-91924400	Enhancers	NHLF	lung
26	chr10:91923800-91927000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
27	chr10:91923800-91935000	Weak transcription	Esophagus	oesophagus
28	chr10:91924000-91930800	Weak transcription	Primary B cells from cord blood	blood
29	chr10:91924400-91927400	Weak transcription	HMEC	breast
30	chr10:91924400-91928000	Weak transcription	NHLF	lung
31	chr10:91926400-91926800	Enhancers	GM12878-XiMat	blood
32	chr10:91926800-91927200	Flanking Active TSS	GM12878-XiMat	blood
33	chr10:91927000-91927400	Enhancers	Placenta Amnion	Placenta Amnion
34	chr10:91927000-91927800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
35	chr10:91927000-91927800	Enhancers	Osteobl	bone
36	chr10:91927000-91928200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
37	chr10:91927000-91928200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
38	chr10:91927200-91927400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
39	chr10:91927200-91927600	Active TSS	GM12878-XiMat	blood
40	chr10:91927200-91928400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
41	chr10:91927400-91928200	Enhancers	HMEC	breast
42	chr10:91927600-91927800	Flanking Active TSS	GM12878-XiMat	blood
43	chr10:91927800-91929200	Enhancers	GM12878-XiMat	blood
44	chr10:91928000-91928200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
45	chr10:91928000-91928200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
46	chr10:91928000-91928200	Enhancers	NHLF	lung
47	chr10:91928200-91929400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
48	chr10:91928200-91933400	Weak transcription	NHLF	lung
49	chr10:91928200-91934800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
50	chr10:91928400-91934400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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