Variant report

Variant	nsv547625
Chromosome Location	chr1:120422705-120466108
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:531)
CpG islands
(count:735)
Chromatin interactive
region (count:27)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:12)

(count:531 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:120441825-120442392	HepG2	liver:	n/a	n/a
2	ARID3A	chr1:120425053-120425244	K562	blood:	n/a	n/a
3	ARID3A	chr1:120422885-120422997	K562	blood:	n/a	n/a
4	ATF1	chr1:120462961-120463475	K562	blood:	n/a	n/a
5	ATF1	chr1:120426630-120426696	K562	blood:	n/a	n/a
6	BACH1	chr1:120431362-120431386	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr1:120430266-120430308	H1-hESC	embryonic stem cell:	n/a	n/a
8	BHLHE40	chr1:120425148-120425279	K562	blood:	n/a	n/a
9	BHLHE40	chr1:120462981-120463318	K562	blood:	n/a	n/a
10	CCNT2	chr1:120438960-120439212	K562	blood:	n/a	n/a
11	CCNT2	chr1:120422520-120423032	K562	blood:	n/a	n/a
12	CEBPB	chr1:120458293-120458452	HepG2	liver:	n/a	chr1:120458392-120458403
13	CEBPB	chr1:120436959-120437216	HepG2	liver:	n/a	n/a
14	CEBPB	chr1:120437715-120437953	A549	lung:	n/a	chr1:120437871-120437882
15	CEBPB	chr1:120438377-120438610	H1-hESC	embryonic stem cell:	n/a	chr1:120438422-120438433
16	CEBPB	chr1:120437729-120438045	HepG2	liver:	n/a	chr1:120437871-120437882
17	CEBPB	chr1:120438300-120438558	HepG2	liver:	n/a	chr1:120438422-120438433
18	CEBPB	chr1:120435966-120436164	HepG2	liver:	n/a	n/a
19	CEBPB	chr1:120425874-120425955	HepG2	liver:	n/a	n/a
20	CEBPD	chr1:120462831-120463263	K562	blood:	n/a	n/a
21	CEBPD	chr1:120425438-120425856	K562	blood:	n/a	n/a
22	CEBPD	chr1:120462907-120463321	K562	blood:	n/a	n/a
23	CREB1	chr1:120428735-120429177	H1-hESC	embryonic stem cell:	n/a	n/a
24	CTCF	chr1:120429500-120429650	GM12873	blood:	n/a	n/a
25	CTCF	chr1:120438940-120439090	HEEpiC	esophagus:	n/a	n/a
26	CTCF	chr1:120438920-120439070	AoAF	blood vessel:	n/a	n/a
27	CTCF	chr1:120438940-120439090	HPAF	blood vessel:	n/a	n/a
28	CTCF	chr1:120439460-120439610	HepG2	liver:	n/a	n/a
29	CTCF	chr1:120428661-120428780	GM19238	blood:	n/a	chr1:120428706-120428719
30	CTCF	chr1:120428880-120429030	HCM	heart:	n/a	n/a
31	CTCF	chr1:120428920-120429070	GM12871	blood:	n/a	n/a
32	CTCF	chr1:120428638-120428647	Spleen_OC	spleen:	n/a	n/a
33	CTCF	chr1:120438900-120439050	HBMEC	blood vessel:	n/a	n/a
34	CTCF	chr1:120428827-120429112	MCF-7	breast:	n/a	n/a
35	CTCF	chr1:120428847-120429077	Spleen_OC	spleen:	n/a	n/a
36	CTCF	chr1:120428900-120429050	GM12864	blood:	n/a	n/a
37	CTCF	chr1:120428859-120429082	GM10248	blood:	n/a	n/a
38	CTCF	chr1:120428880-120429030	AG09309	skin:	n/a	n/a
39	CTCF	chr1:120428840-120428990	GM12867	blood:	n/a	n/a
40	CTCF	chr1:120438920-120439070	AG04449	skin:	n/a	n/a
41	CTCF	chr1:120438960-120439110	AG09309	skin:	n/a	n/a
42	CTCF	chr1:120438880-120439030	BJ	skin:	n/a	n/a
43	CTCF	chr1:120438914-120439183	H1-hESC	embryonic stem cell:	n/a	n/a
44	CTCF	chr1:120428860-120429010	HRE	kidney:	n/a	n/a
45	CTCF	chr1:120428900-120429050	HPAF	blood vessel:	n/a	n/a
46	CTCF	chr1:120428920-120429070	WERI-Rb-1	eye:	n/a	n/a
47	CTCF	chr1:120438920-120439070	GM12866	blood:	n/a	n/a
48	CTCF	chr1:120438920-120439070	HCM	heart:	n/a	n/a
49	CTCF	chr1:120428543-120429302	A549	lung:	n/a	chr1:120428706-120428719
50	CTCF	chr1:120439020-120439170	RPTEC	kidney:	n/a	n/a

(count:735 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:120439396-120439446	CMK	blood:	n/a
2	chr1:120457856-120457906	PFSK-1	brain:	n/a
3	chr1:120439870-120439920	AG09309	skin:	n/a
4	chr1:120439396-120439446	CMK	blood:	n/a
5	chr1:120457856-120457906	PFSK-1	brain:	n/a
6	chr1:120439870-120439920	AG09309	skin:	n/a
7	chr1:120439396-120439446	AG10803	skin:	n/a
8	chr1:120441702-120441752	BE2_C	brain:	n/a
9	chr1:120438925-120438975	HRE	kidney:	n/a
10	chr1:120439036-120439086	PANC-1	pancreas:	n/a
11	chr1:120457856-120457906	HCF	heart:	n/a
12	chr1:120439522-120439572	GM12878	blood:	n/a
13	chr1:120439522-120439572	ECC-1	luminal epithelium:	n/a
14	chr1:120439014-120439064	NHBE	bronchial:	n/a
15	chr1:120439014-120439064	HIPEpiC	eye:	n/a
16	chr1:120441702-120441752	HCPEpiC	choroid plexus:	n/a
17	chr1:120437090-120437140	HEEpiC	esophagus:	n/a
18	chr1:120440230-120440280	HCPEpiC	choroid plexus:	n/a
19	chr1:120441702-120441752	Caco-2	colon:	n/a
20	chr1:120457856-120457906	NHBE	bronchial:	n/a
21	chr1:120437090-120437140	HRPEpiC	eye:	n/a
22	chr1:120439014-120439064	IMR90	lung:	fetal
23	chr1:120439522-120439572	HIPEpiC	eye:	n/a
24	chr1:120439014-120439064	HMEC	breast:	n/a
25	chr1:120439870-120439920	HNPCEpiC	eye:	n/a
26	chr1:120457856-120457906	BJ	skin:	n/a
27	chr1:120440230-120440280	PANC-1	pancreas:	n/a
28	chr1:120435245-120435295	NH-A	brain:	n/a
29	chr1:120438925-120438975	HEEpiC	esophagus:	n/a
30	chr1:120439036-120439086	GM12892	blood:	n/a
31	chr1:120440230-120440280	NHDF-neo	bronchial:	n/a
32	chr1:120439014-120439064	SAEC	small airway:	n/a
33	chr1:120439014-120439064	AG10803	skin:	n/a
34	chr1:120441702-120441752	HRCEpiC	kidney:	n/a
35	chr1:120440230-120440280	GM06990	blood:	n/a
36	chr1:120439396-120439446	ovcar-3	ovarian:	n/a
37	chr1:120439014-120439064	T-47D	breast:	n/a
38	chr1:120439812-120439862	NB4	blood:	n/a
39	chr1:120438925-120438975	NH-A	brain:	n/a
40	chr1:120439036-120439086	NB4	blood:	n/a
41	chr1:120439870-120439920	MCF-7	breast:	n/a
42	chr1:120457856-120457906	NB4	blood:	n/a
43	chr1:120439522-120439572	HRPEpiC	eye:	n/a
44	chr1:120437090-120437140	HMEC	breast:	n/a
45	chr1:120440230-120440280	Hepatocyte	liver:	n/a
46	chr1:120441702-120441752	HUVEC	blood vessel:	n/a
47	chr1:120437090-120437140	AG04449	skin:	fetal
48	chr1:120439870-120439920	RPTEC	kidney:	n/a
49	chr1:120457856-120457906	HUVEC	blood vessel:	n/a
50	chr1:120438925-120438975	HEK293	kidney:	embryo

(count:27 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:120445705..120448547-chr1:120448757..120452152,3	MCF-7	breast:
2	chr1:120438934..120440832-chr1:120445374..120447233,2	K562	blood:
3	chr1:120436002..120438494-chr1:120462381..120464792,2	MCF-7	breast:
4	chr1:120449201..120451980-chr1:120452971..120455460,2	MCF-7	breast:
5	chr1:120445668..120448303-chr1:120496593..120499239,2	MCF-7	breast:
6	chr1:120440889..120443240-chr12:109181998..109184664,2	MCF-7	breast:
7	chr1:120440403..120442887-chr1:120444979..120447049,2	MCF-7	breast:
8	chr1:120426879..120429312-chr1:120432285..120434673,2	MCF-7	breast:
9	chr1:120444002..120446345-chr1:120453344..120455730,3	MCF-7	breast:
10	chr1:120428374..120430929-chr1:144532739..144535945,3	K562	blood:
11	chr1:120461834..120464698-chr1:120475865..120478415,2	MCF-7	breast:
12	chr1:120440403..120442887-chr1:120444979..120447049,2	MCF-7	breast:
13	chr1:120447256..120450228-chr1:120525932..120527487,2	K562	blood:
14	chr1:120400878..120403434-chr1:120429544..120432344,2	MCF-7	breast:
15	chr1:120455729..120458677-chr1:120465147..120468544,4	MCF-7	breast:
16	chr1:120461841..120464545-chr1:120468138..120469880,2	MCF-7	breast:
17	chr1:120454474..120456790-chr1:120460931..120463931,3	MCF-7	breast:
18	chr1:120454474..120456790-chr1:120460931..120463931,3	MCF-7	breast:
19	chr1:120449760..120452245-chrX:18130620..18132924,2	MCF-7	breast:
20	chr1:120444002..120446345-chr1:120453344..120455730,3	MCF-7	breast:
21	chr1:120456262..120460550-chr1:120460767..120463877,3	K562	blood:
22	chr1:120423918..120425680-chr1:120436272..120439121,2	MCF-7	breast:
23	chr1:120436002..120438494-chr1:120462381..120464792,2	MCF-7	breast:
24	chr1:120445705..120448547-chr1:120448757..120452152,3	MCF-7	breast:
25	chr1:120452541..120455108-chr1:120461853..120464281,3	K562	blood:
26	chr1:120456262..120460550-chr1:120460767..120463877,3	K562	blood:
27	chr1:120450368..120452473-chr1:120481049..120483944,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NOTCH2-1	chr1:120451878-120453236	ENSG00000261662.1

No data

(count:12 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	NOTCH2	hsa-miR-34a-5p	chr1:120455456-120455477
2	NOTCH2	hsa-miR-16-5p	chr1:120457884-120457878
3	NOTCH2	hsa-miR-107	chr1:120457885-120457879
4	NOTCH2	hsa-miR-107	chr1:120457879-120457900
5	NOTCH2	hsa-miR-181c-5p	chr1:120454955-120454976
6	NOTCH2	hsa-miR-181a-5p	chr1:120454961-120454954
7	NOTCH2	hsa-miR-181c-5p	chr1:120454961-120454954
8	NOTCH2	hsa-miR-326	chr1:120454916-120454935
9	NOTCH2	hsa-miR-1	chr1:120454297-120454318
10	NOTCH2	hsa-miR-181a-5p	chr1:120454955-120454976
11	NOTCH2	hsa-miR-34a-5p	chr1:120455462-120455456
12	NOTCH2	hsa-miR-16-5p	chr1:120457878-120457901

Variant related genes	Relation type
ADAM30	TF binding region
ENSG00000261662	TF binding region
NOTCH2P1	TF binding region
ADAM30	CpG island
ENSG00000261662	CpG island
NOTCH2P1	CpG island
ENSG00000201699	chromatin interactions
ENSG00000261662	chromatin interactions
ENSG00000134249	chromatin interactions
ENSG00000134250	chromatin interactions
ENSG00000226446	chromatin interactions

Extended variants
information (count: 1446 )
Associated
traits (count: 85 )

Variant overlapped rSNPs/rCNVs (count:1446 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4659246	chr1:120422705-120422706	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs35848365	chr1:120422711-120422712	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs587652489	chr1:120422726-120422727	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs185344095	chr1:120422810-120422811	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs12061487	chr1:120422838-120422839	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs587655204	chr1:120422855-120422856	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs191279881	chr1:120422882-120422883	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs181346133	chr1:120422885-120422886	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs186663350	chr1:120422897-120422898	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs587600158	chr1:120422908-120422909	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs587670435	chr1:120422917-120422918	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs587710573	chr1:120422952-120422953	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs12061529	chr1:120422965-120422966	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs191504801	chr1:120423015-120423016	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs145767446	chr1:120423024-120423025	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs183038086	chr1:120423137-120423138	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs587762463	chr1:120423143-120423144	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs138960844	chr1:120423158-120423159	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs28546096	chr1:120423187-120423188	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs587731000	chr1:120423195-120423196	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs187755450	chr1:120423214-120423215	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs151297787	chr1:120423217-120423218	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs2487581	chr1:120423226-120423227	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs2487582	chr1:120423228-120423229	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs587655089	chr1:120423230-120423231	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs190912633	chr1:120423243-120423244	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs138035564	chr1:120423407-120423408	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs587646465	chr1:120423419-120423420	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs368069478	chr1:120423533-120423534	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs182077434	chr1:120423561-120423562	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs74115382	chr1:120423570-120423571	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs587727589	chr1:120423594-120423595	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs587623433	chr1:120423742-120423743	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs587682686	chr1:120423778-120423779	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs186713093	chr1:120423830-120423831	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs587597980	chr1:120423842-120423843	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs368860064	chr1:120423867-120423868	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs587673988	chr1:120423878-120423879	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs587740216	chr1:120423889-120423890	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs587619708	chr1:120423895-120423896	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs192858932	chr1:120423902-120423903	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs184661216	chr1:120423916-120423917	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs587632753	chr1:120423959-120423960	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs188400834	chr1:120424021-120424022	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs587768819	chr1:120424024-120424025	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs587608577	chr1:120424053-120424054	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs376550375	chr1:120424063-120424064	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs587746425	chr1:120424064-120424065	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs587650283	chr1:120424090-120424091	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs201464801	chr1:120424181-120424182	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:85)

Disease	PMID	Source
Wilms tumour	21544195	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
Glioblastoma multiforme	21080181	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
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	22495311	CNVD
Chordoma	21602918	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Melanoma	18172304	CNVD
Multiple myeloma	16461302	CNVD
Cancer	21129771	CNVD
Non-small cell lung cancer	21385341	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
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Medulloblastoma	21979893	CNVD
Cervical cancer	21062161	CNVD
Cancer	21183584	CNVD
Lung cancer	18438408	CNVD
Rett syndrome	21593744	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Aetanephric adenomas	20802469	CNVD
Multiple myeloma	16616336	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Systemic lupus erythematosus	21956041	CNVD
Breast cancer	21804112	CNVD
Mental retardation	21062444	CNVD
Myelofibrosis	22110671	CNVD
Emphysema	19352772	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21858162	CNVD
Follicular lymphoma	18703704	CNVD
Breast cancer	21509527	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Aortic dissecting aneurysms	22263138	CNVD
Schizophrenia	21346763	CNVD

Chromatin state (count:489 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:120420400-120424400	Weak transcription	Monocytes-CD14+_RO01746	blood
2	chr1:120422200-120422800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
3	chr1:120422200-120423200	Enhancers	K562	blood
4	chr1:120422600-120423000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
5	chr1:120423000-120424800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
6	chr1:120423200-120425000	Weak transcription	K562	blood
7	chr1:120423600-120424800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
8	chr1:120424400-120424800	Enhancers	Monocytes-CD14+_RO01746	blood
9	chr1:120424600-120428400	Enhancers	Primary monocytes fromperipheralblood	blood
10	chr1:120424800-120425000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
11	chr1:120424800-120425200	Enhancers	Rectal Mucosa Donor 31	rectum
12	chr1:120424800-120425600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
13	chr1:120424800-120425600	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
14	chr1:120424800-120425600	Enhancers	NHDF-Ad	bronchial
15	chr1:120424800-120427600	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
16	chr1:120424800-120428400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
17	chr1:120425000-120425400	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
18	chr1:120425000-120425400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
19	chr1:120425000-120425400	Enhancers	Osteobl	bone
20	chr1:120425000-120425600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
21	chr1:120425000-120425600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
22	chr1:120425000-120427600	Enhancers	K562	blood
23	chr1:120425200-120425400	Enhancers	Adipose Nuclei	Adipose
24	chr1:120425400-120426000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
25	chr1:120425400-120427200	Weak transcription	Adipose Nuclei	Adipose
26	chr1:120425400-120427200	Weak transcription	Osteobl	bone
27	chr1:120425600-120427000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
28	chr1:120425600-120427000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
29	chr1:120425600-120427200	Weak transcription	NHDF-Ad	bronchial
30	chr1:120426000-120427000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
31	chr1:120426600-120428200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
32	chr1:120427000-120427400	Enhancers	Primary hematopoietic stem cells	blood
33	chr1:120427000-120427400	Enhancers	Brain Cingulate Gyrus	brain
34	chr1:120427000-120428200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
35	chr1:120427000-120428200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
36	chr1:120427000-120428400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
37	chr1:120427200-120427400	Bivalent Enhancer	IMR90 fetal lung fibroblasts Cell Line	lung
38	chr1:120427200-120428000	Enhancers	Adipose Nuclei	Adipose
39	chr1:120427200-120428000	Enhancers	Osteobl	bone
40	chr1:120427200-120428200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
41	chr1:120427200-120428200	Enhancers	NHDF-Ad	bronchial
42	chr1:120427600-120428000	Enhancers	Primary hematopoietic stem cells short term culture	blood
43	chr1:120427600-120428600	Enhancers	Monocytes-CD14+_RO01746	blood
44	chr1:120428600-120428800	Enhancers	Aorta	Aorta
45	chr1:120428600-120429000	Enhancers	Liver	Liver
46	chr1:120428800-120430400	Weak transcription	Aorta	Aorta
47	chr1:120430400-120431000	ZNF genes & repeats	Aorta	Aorta
48	chr1:120433400-120435800	Enhancers	Dnd41	blood
49	chr1:120435600-120436800	Enhancers	HepG2	liver
50	chr1:120435600-120437600	Enhancers	Pancreas	Pancrea

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