Variant report

Variant	nsv525678
Chromosome Location	chr1:86487914-86549498
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:177)
CpG islands
(count:61)
Chromatin interactive
region (count:4)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:177 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CEBPB	chr1:86522930-86523465	IMR90	lung:	n/a	n/a
2	CEBPB	chr1:86516886-86517187	IMR90	lung:	n/a	chr1:86517014-86517025
3	CEBPB	chr1:86511915-86512044	A549	lung:	n/a	n/a
4	CEBPB	chr1:86535599-86535705	IMR90	lung:	n/a	n/a
5	CEBPB	chr1:86497465-86497549	K562	blood:	n/a	chr1:86497510-86497519 chr1:86497510-86497519 chr1:86497510-86497519 chr1:86497508-86497521 chr1:86497510-86497519 chr1:86497510-86497521
6	CEBPB	chr1:86516868-86517205	HepG2	liver:	n/a	chr1:86517014-86517025
7	CEBPB	chr1:86516910-86517192	A549	lung:	n/a	chr1:86517014-86517025
8	CEBPB	chr1:86516871-86517178	K562	blood:	n/a	chr1:86517014-86517025
9	CTCF	chr1:86535000-86535150	NHLF	lung:	n/a	n/a
10	CTCF	chr1:86548040-86548190	AG04450	lung:	n/a	n/a
11	CTCF	chr1:86548094-86548124	LNCaP	prostate:	n/a	n/a
12	CTCF	chr1:86547980-86548130	HCPEpiC	choroid plexus:	n/a	n/a
13	CTCF	chr1:86548062-86548145	HepG2	liver:	n/a	n/a
14	CTCF	chr1:86547980-86548190	GM12871	blood:	n/a	n/a
15	CTCF	chr1:86547920-86548070	AG04450	lung:	n/a	n/a
16	CTCF	chr1:86547960-86548110	GM12872	blood:	n/a	n/a
17	CTCF	chr1:86548000-86548150	SK-N-SH_RA	brain:	n/a	n/a
18	CTCF	chr1:86548020-86548170	GM12872	blood:	n/a	n/a
19	CTCF	chr1:86547880-86548110	GM12878	blood:	n/a	n/a
20	CTCF	chr1:86545691-86545784	GM20000	blood:	n/a	n/a
21	CTCF	chr1:86547980-86548130	BE2_C	brain:	n/a	n/a
22	CTCF	chr1:86548040-86548190	HA-sp	spinal cord:	n/a	n/a
23	CTCF	chr1:86548120-86548270	HCM	heart:	n/a	n/a
24	CTCF	chr1:86548020-86548170	WERI-Rb-1	eye:	n/a	n/a
25	CTCF	chr1:86547992-86548180	GM12878	blood:	n/a	n/a
26	CTCF	chr1:86548040-86548190	AoAF	blood vessel:	n/a	n/a
27	CTCF	chr1:86548020-86548170	AG04449	skin:	n/a	n/a
28	CTCF	chr1:86547937-86548210	IMR90	lung:	n/a	n/a
29	CTCF	chr1:86548000-86548150	HPF	lung:	n/a	n/a
30	CTCF	chr1:86518184-86518210	Lung_OC	lung:	n/a	n/a
31	CTCF	chr1:86548040-86548190	RPTEC	kidney:	n/a	n/a
32	CTCF	chr1:86548020-86548170	HEK293	kidney:	n/a	n/a
33	CTCF	chr1:86548020-86548170	GM12864	blood:	n/a	n/a
34	CTCF	chr1:86548020-86548170	SAEC	small airway:	n/a	n/a
35	CTCF	chr1:86504084-86504139	Kidney_OC	kidney:	n/a	n/a
36	CTCF	chr1:86548020-86548170	HEEpiC	esophagus:	n/a	n/a
37	CTCF	chr1:86547994-86548173	HUVEC	blood vessel:	n/a	n/a
38	CTCF	chr1:86547980-86548130	HVMF	connective:	n/a	n/a
39	CTCF	chr1:86547960-86548110	HMF	breast:	n/a	n/a
40	CTCF	chr1:86547962-86548251	GM12878	blood:	n/a	n/a
41	CTCF	chr1:86547980-86548130	HFF-Myc	foreskin:	n/a	n/a
42	CTCF	chr1:86548020-86548170	HRE	kidney:	n/a	n/a
43	CTCF	chr1:86548020-86548145	GM13977	blood:	n/a	n/a
44	CTCF	chr1:86548064-86548143	MCF-7	breast:	n/a	n/a
45	CTCF	chr1:86548080-86548230	NB4	blood:	n/a	n/a
46	CTCF	chr1:86547940-86548090	HCT-116	colon:	n/a	n/a
47	CTCF	chr1:86547940-86548090	HepG2	liver:	n/a	n/a
48	CTCF	chr1:86547980-86548130	HRPEpiC	eye:	n/a	n/a
49	CTCF	chr1:86548000-86548150	HBMEC	blood vessel:	n/a	n/a
50	CTCF	chr1:86547980-86548130	Hela-S3	cervix:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:86534132-86534182	HRE	kidney:	n/a
2	chr1:86534132-86534182	AoSMC	blood vessel:	n/a
3	chr1:86534132-86534182	SAEC	small airway:	n/a
4	chr1:86534132-86534182	ECC-1	luminal epithelium:	n/a
5	chr1:86534132-86534182	Jurkat	blood:	n/a
6	chr1:86534132-86534182	PFSK-1	brain:	n/a
7	chr1:86534132-86534182	AG09309	skin:	n/a
8	chr1:86534132-86534182	PrEC	prostate:	n/a
9	chr1:86534132-86534182	GM19239	blood:	n/a
10	chr1:86534132-86534182	HPAEpiC	pulmonary alveolar:	n/a
11	chr1:86534132-86534182	HCT-116	colon:	n/a
12	chr1:86534132-86534182	HCF	heart:	n/a
13	chr1:86534132-86534182	HIPEpiC	eye:	n/a
14	chr1:86534132-86534182	U87	brain:	n/a
15	chr1:86534132-86534182	GM12892	blood:	n/a
16	chr1:86534132-86534182	MCF-7	breast:	n/a
17	chr1:86534132-86534182	GM06990	blood:	n/a
18	chr1:86534132-86534182	CMK	blood:	n/a
19	chr1:86534132-86534182	HAEpiC	amniotic membrane:	n/a
20	chr1:86534132-86534182	NHDF-neo	bronchial:	n/a
21	chr1:86534132-86534182	T-47D	breast:	n/a
22	chr1:86534132-86534182	HEEpiC	esophagus:	n/a
23	chr1:86534132-86534182	BE2_C	brain:	n/a
24	chr1:86534132-86534182	SK-N-SH_RA	brain:	n/a
25	chr1:86534132-86534182	MCF10A-Er-Src	breast:	n/a
26	chr1:86534132-86534182	GM12891	blood:	n/a
27	chr1:86534132-86534182	IMR90	lung:	fetal
28	chr1:86534132-86534182	ProgFib	skin:	n/a
29	chr1:86534132-86534182	NHBE	bronchial:	n/a
30	chr1:86534132-86534182	AG10803	skin:	n/a
31	chr1:86534132-86534182	H1-hESC	embryonic stem cell:	embryo
32	chr1:86534132-86534182	K562	blood:	n/a
33	chr1:86534132-86534182	HCPEpiC	choroid plexus:	n/a
34	chr1:86534132-86534182	HRCEpiC	kidney:	n/a
35	chr1:86534132-86534182	A549	lung:	n/a
36	chr1:86534132-86534182	HCM	heart:	n/a
37	chr1:86534132-86534182	SK-N-MC	brain:	n/a
38	chr1:86534132-86534182	AG04449	skin:	fetal
39	chr1:86534132-86534182	BJ	skin:	n/a
40	chr1:86534132-86534182	HMEC	breast:	n/a
41	chr1:86534132-86534182	SK-N-SH	brain:	n/a
42	chr1:86534132-86534182	HUVEC	blood vessel:	n/a
43	chr1:86534132-86534182	NT2-D1	testis:	n/a
44	chr1:86534132-86534182	HRPEpiC	eye:	n/a
45	chr1:86534132-86534182	NB4	blood:	n/a
46	chr1:86534132-86534182	LNCaP	prostate:	n/a
47	chr1:86534132-86534182	Hela-S3	cervix:	n/a
48	chr1:86534132-86534182	GM12878	blood:	n/a
49	chr1:86534132-86534182	Caco-2	colon:	n/a
50	chr1:86534132-86534182	HepG2	liver:	n/a

(count:4 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:86516859..86518628-chr1:86521588..86524119,2	K562	blood:
2	chr1:86478740..86480612-chr1:86522997..86525923,2	K562	blood:
3	chr1:86483581..86486265-chr1:86488492..86490836,2	K562	blood:
4	chr1:86516859..86518628-chr1:86521588..86524119,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CLCA2-1	chr1:86495537-86496272	NONHSAT004263

No data

Variant related genes	Relation type
ENSG00000229505	TF binding region
ENSG00000229505	CpG island

Extended variants
information (count: 2305 )
Associated
traits (count: 97 )

Variant overlapped rSNPs/rCNVs (count:2305 , 50 per page) page: 1 2 3 4 5 6 7 ... 47

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11161721	chr1:86487914-86487915	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs371662746	chr1:86487924-86487925	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs200157113	chr1:86487927-86487928	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs539755418	chr1:86487942-86487943	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs201423819	chr1:86487952-86487953	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs369573090	chr1:86487954-86487955	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs377276430	chr1:86487956-86487957	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs199668151	chr1:86487957-86487958	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs386633130	chr1:86487981-86487982	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs199869127	chr1:86487990-86487991	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs200977491	chr1:86487991-86487992	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs202206189	chr1:86487992-86487993	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs35501628	chr1:86487993-86487994	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs386367559	chr1:86487994-86487995	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs397741763	chr1:86487997-86487998	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs541847871	chr1:86488030-86488031	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs549338317	chr1:86488043-86488044	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs192049470	chr1:86488066-86488067	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs75357114	chr1:86488081-86488082	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs376360593	chr1:86488091-86488092	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs572188343	chr1:86488152-86488153	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs541102258	chr1:86488154-86488155	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs138117415	chr1:86488157-86488158	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs369791694	chr1:86488179-86488180	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs373130063	chr1:86488190-86488191	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs201983840	chr1:86488207-86488208	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs376096881	chr1:86488221-86488222	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs641712	chr1:86488232-86488233	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
29	rs201569788	chr1:86488239-86488240	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs201118131	chr1:86488251-86488252	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs370749711	chr1:86488265-86488266	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs563038545	chr1:86488292-86488293	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs374156945	chr1:86488305-86488306	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs199532528	chr1:86488314-86488315	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs557626969	chr1:86488345-86488346	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs184149680	chr1:86488352-86488353	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs147311414	chr1:86488430-86488431	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs548192418	chr1:86488485-86488486	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs12136419	chr1:86488496-86488497	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs568085561	chr1:86488516-86488517	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs377029827	chr1:86488556-86488557	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs200015039	chr1:86488559-86488560	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs570663338	chr1:86488592-86488593	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs539251474	chr1:86488602-86488603	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs149329527	chr1:86488605-86488606	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs576265019	chr1:86488622-86488623	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs367693606	chr1:86488628-86488629	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs200499255	chr1:86488689-86488690	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs535715779	chr1:86488737-86488738	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs375862286	chr1:86488796-86488797	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:97)

Disease	PMID	Source
Colorectal cancer	16272173	CNVD
Medulloblastoma	21979893	CNVD
Wilms tumour	21544195	CNVD
Coronary Disease	20032323	CNVD
Prostate cancer	21965145	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Stargardt''s disease	17277736	CNVD
Neuroblastoma	17897457	CNVD
Uveal melanoma	21693616	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-syndromic sensorineural hearing loss	22290220	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	21264507	CNVD
Acute myeloid leukemia	16864856	CNVD
Astrocytoma	17387387	CNVD
Cancer	21499728	CNVD
Glioblastoma multiforme	17387387	CNVD
Oligodendroglial tumors	17285580	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Neuroblastoma	17535989	CNVD
Pheochromocytoma	17535989	CNVD
Prostate cancer	16705090	CNVD
Astrocytoma	17934521	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Neuroblastoma	17533364	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	22495311	CNVD
Non-small cell lung cancer	21385341	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Chordoma	21602918	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Melanoma	18172304	CNVD
Multiple myeloma	16461302	CNVD
Cancer	21129771	CNVD
Autosomal dominant nocturnal frontal lobe epilepsy	18472482	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-small cell lung cancer	20864512	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Thrombocytopenia-absent radius syndrome	21933853	CNVD
Psychiatric disorder	22848183	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	20409316	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Cervical cancer	21062161	CNVD
Cancer	21183584	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21364760	CNVD
Rett syndrome	21593744	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	16608533	CNVD
Ovarian cancer	21720365	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Ewing''s sarcoma	17952124	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Cancer	22429812	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Breast cancer	17133270	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Multiple myeloma	17550852	CNVD
Myelofibrosis	22110671	CNVD
Neuroblastoma	21899760	CNVD
Breast cancer	16397240	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Esophageal adenocarcinoma	18820669	CNVD
small cell lung cancer	20016488	CNVD
Glioma	20126413	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:114 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:86484600-86489400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
2	chr1:86487600-86488200	Strong transcription	Fetal Lung	lung
3	chr1:86488200-86493000	Weak transcription	Fetal Lung	lung
4	chr1:86493000-86493800	Weak transcription	Fetal Muscle Trunk	muscle
5	chr1:86493000-86494200	Strong transcription	Fetal Lung	lung
6	chr1:86494200-86506800	Weak transcription	Fetal Lung	lung
7	chr1:86497800-86498000	Enhancers	Aorta	Aorta
8	chr1:86503000-86503200	Enhancers	Fetal Intestine Large	intestine
9	chr1:86506600-86508600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
10	chr1:86506800-86507800	Enhancers	Fetal Lung	lung
11	chr1:86507000-86507400	Enhancers	Rectal Smooth Muscle	rectum
12	chr1:86507000-86507600	Enhancers	Colon Smooth Muscle	Colon
13	chr1:86507200-86508000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
14	chr1:86507400-86507800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
15	chr1:86507800-86520400	Weak transcription	Fetal Lung	lung
16	chr1:86517000-86517400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
17	chr1:86517400-86519200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
18	chr1:86518200-86519800	Enhancers	GM12878-XiMat	blood
19	chr1:86518600-86518800	Enhancers	NHLF	lung
20	chr1:86519200-86519800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
21	chr1:86519400-86519600	Enhancers	NHLF	lung
22	chr1:86519800-86522000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
23	chr1:86520000-86520200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
24	chr1:86520400-86521000	Strong transcription	Fetal Lung	lung
25	chr1:86520800-86521000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
26	chr1:86521000-86527200	Weak transcription	Fetal Lung	lung
27	chr1:86522000-86523000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
28	chr1:86522800-86523000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
29	chr1:86522800-86523000	Enhancers	Psoas Muscle	Psoas
30	chr1:86523000-86533800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
31	chr1:86526800-86528600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
32	chr1:86527000-86527600	Enhancers	GM12878-XiMat	blood
33	chr1:86527000-86528600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
34	chr1:86527000-86528800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
35	chr1:86527000-86528800	Enhancers	Osteobl	bone
36	chr1:86527200-86527600	Enhancers	Fetal Lung	lung
37	chr1:86527200-86527800	Enhancers	Monocytes-CD14+_RO01746	blood
38	chr1:86527200-86528000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
39	chr1:86527200-86528600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
40	chr1:86527200-86528600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
41	chr1:86527400-86527800	Enhancers	Primary monocytes fromperipheralblood	blood
42	chr1:86527600-86528600	Enhancers	Muscle Satellite Cultured Cells	--
43	chr1:86527600-86530000	Weak transcription	Fetal Lung	lung
44	chr1:86528200-86528400	Enhancers	Fetal Muscle Leg	muscle
45	chr1:86528600-86533200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
46	chr1:86528600-86533200	Weak transcription	Muscle Satellite Cultured Cells	--
47	chr1:86528600-86534000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
48	chr1:86528800-86533000	Weak transcription	Osteobl	bone
49	chr1:86530000-86530200	Enhancers	Fetal Lung	lung
50	chr1:86530200-86530600	Weak transcription	Fetal Lung	lung

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