Variant report

Variant	nsv1006447
Chromosome Location	chr1:120123722-120154798
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	ATF1	chr1:120125462-120125747	K562	blood:	n/a	n/a
2	ATF1	chr1:120151890-120151896	K562	blood:	n/a	n/a
3	ATF3	chr1:120154276-120154532	K562	blood:	n/a	n/a
4	ATF3	chr1:120154165-120154614	H1-hESC	embryonic stem cell:	n/a	n/a
5	BHLHE40	chr1:120154235-120154668	K562	blood:	n/a	n/a
6	BRCA1	chr1:120125543-120125709	Hela-S3	cervix:	n/a	n/a
7	CEBPB	chr1:120152140-120152301	H1-hESC	embryonic stem cell:	n/a	chr1:120152213-120152224
8	CEBPB	chr1:120152171-120152183	HepG2	liver:	n/a	n/a
9	CEBPB	chr1:120144827-120145081	Hela-S3	cervix:	n/a	chr1:120144889-120144900
10	CEBPB	chr1:120144744-120145076	A549	lung:	n/a	chr1:120144889-120144900
11	CEBPB	chr1:120152150-120152238	K562	blood:	n/a	chr1:120152213-120152224
12	CEBPB	chr1:120154268-120154461	Hela-S3	cervix:	n/a	n/a
13	CEBPB	chr1:120144741-120145077	HepG2	liver:	n/a	chr1:120144889-120144900
14	CEBPB	chr1:120142586-120142702	H1-hESC	embryonic stem cell:	n/a	n/a
15	CEBPB	chr1:120144888-120144965	H1-hESC	embryonic stem cell:	n/a	chr1:120144889-120144900
16	CHD2	chr1:120154302-120154481	Hela-S3	cervix:	n/a	n/a
17	CHD2	chr1:120154059-120154552	H1-hESC	embryonic stem cell:	n/a	n/a
18	CTCF	chr1:120154340-120154490	GM12874	blood:	n/a	chr1:120154411-120154432
19	CTCF	chr1:120154340-120154490	GM12866	blood:	n/a	chr1:120154411-120154432
20	CTCF	chr1:120149960-120150110	GM12872	blood:	n/a	n/a
21	CTCF	chr1:120125560-120125710	RPTEC	kidney:	n/a	chr1:120125618-120125631 chr1:120125615-120125633 chr1:120125617-120125638
22	CTCF	chr1:120154320-120154470	AG04450	lung:	n/a	chr1:120154411-120154432
23	CTCF	chr1:120125543-120125690	GM10248	blood:	n/a	chr1:120125618-120125631 chr1:120125615-120125633 chr1:120125617-120125638
24	CTCF	chr1:120154360-120154510	Hela-S3	cervix:	n/a	chr1:120154411-120154432
25	CTCF	chr1:120154253-120154541	A549	lung:	n/a	chr1:120154411-120154432
26	CTCF	chr1:120125503-120125747	NHEK	skin:	n/a	chr1:120125618-120125631 chr1:120125615-120125633 chr1:120125617-120125638
27	CTCF	chr1:120154270-120154536	GM13977	blood:	n/a	chr1:120154411-120154432
28	CTCF	chr1:120130255-120130277	GM20000	blood:	n/a	n/a
29	CTCF	chr1:120154320-120154470	NHLF	lung:	n/a	chr1:120154411-120154432
30	CTCF	chr1:120154689-120154733	ProgFib	skin:	n/a	n/a
31	CTCF	chr1:120125502-120125797	SK-N-SH_RA	brain:	n/a	chr1:120125618-120125631 chr1:120125615-120125633 chr1:120125617-120125638
32	CTCF	chr1:120125840-120125990	WERI-Rb-1	eye:	n/a	n/a
33	CTCF	chr1:120150182-120150326	GM13976	blood:	n/a	chr1:120150241-120150262 chr1:120150240-120150256 chr1:120150239-120150257 chr1:120150242-120150255
34	CTCF	chr1:120150060-120150210	SAEC	small airway:	n/a	n/a
35	CTCF	chr1:120154320-120154470	WI-38	lung:	n/a	chr1:120154411-120154432
36	CTCF	chr1:120154320-120154470	HBMEC	blood vessel:	n/a	chr1:120154411-120154432
37	CTCF	chr1:120154276-120154532	MCF-7	breast:	n/a	chr1:120154411-120154432
38	CTCF	chr1:120125540-120125690	GM12878	blood:	n/a	chr1:120125618-120125631 chr1:120125615-120125633 chr1:120125617-120125638
39	CTCF	chr1:120125521-120125719	GM19240	blood:	n/a	chr1:120125618-120125631 chr1:120125615-120125633 chr1:120125617-120125638
40	CTCF	chr1:120125500-120125750	HUVEC	blood vessel:	n/a	chr1:120125618-120125631 chr1:120125615-120125633 chr1:120125617-120125638
41	CTCF	chr1:120125540-120125690	GM12865	blood:	n/a	chr1:120125618-120125631 chr1:120125615-120125633 chr1:120125617-120125638
42	CTCF	chr1:120154320-120154470	GM12871	blood:	n/a	chr1:120154411-120154432
43	CTCF	chr1:120154265-120154537	MCF-7	breast:	n/a	chr1:120154411-120154432
44	CTCF	chr1:120125500-120125650	HEK293	kidney:	n/a	chr1:120125618-120125631 chr1:120125615-120125633 chr1:120125617-120125638
45	CTCF	chr1:120154264-120154561	A549	lung:	n/a	chr1:120154411-120154432
46	CTCF	chr1:120150114-120150361	HepG2	liver:	n/a	chr1:120150241-120150262 chr1:120150240-120150256 chr1:120150239-120150257 chr1:120150242-120150255
47	CTCF	chr1:120150060-120150210	HCPEpiC	choroid plexus:	n/a	n/a
48	CTCF	chr1:120154300-120154450	HFF-Myc	foreskin:	n/a	chr1:120154411-120154432
49	CTCF	chr1:120125540-120125690	GM12873	blood:	n/a	chr1:120125618-120125631 chr1:120125615-120125633 chr1:120125617-120125638
50	CTCF	chr1:120125540-120125690	HL-60	blood:	n/a	chr1:120125618-120125631 chr1:120125615-120125633 chr1:120125617-120125638

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:120143242-120143292	SK-N-SH	brain:	n/a
2	chr1:120143242-120143292	Hepatocyte	liver:	n/a
3	chr1:120143242-120143292	IMR90	lung:	fetal
4	chr1:120143242-120143292	BJ	skin:	n/a
5	chr1:120143242-120143292	MCF10A-Er-Src	breast:	n/a
6	chr1:120143242-120143292	H1-hESC	embryonic stem cell:	embryo
7	chr1:120143242-120143292	HPAEpiC	pulmonary alveolar:	n/a
8	chr1:120143242-120143292	AG04450	lung:	fetal
9	chr1:120143242-120143292	GM19239	blood:	n/a
10	chr1:120143242-120143292	CMK	blood:	n/a
11	chr1:120143242-120143292	PFSK-1	brain:	n/a
12	chr1:120143242-120143292	HL-60	blood:	n/a
13	chr1:120143242-120143292	HCF	heart:	n/a
14	chr1:120143242-120143292	GM12892	blood:	n/a
15	chr1:120143242-120143292	HCM	heart:	n/a
16	chr1:120143242-120143292	Caco-2	colon:	n/a
17	chr1:120143242-120143292	NHBE	bronchial:	n/a
18	chr1:120143242-120143292	Hela-S3	cervix:	n/a
19	chr1:120143242-120143292	AG09309	skin:	n/a
20	chr1:120143242-120143292	HepG2	liver:	n/a
21	chr1:120143242-120143292	SK-N-SH_RA	brain:	n/a
22	chr1:120143242-120143292	LNCaP	prostate:	n/a
23	chr1:120143242-120143292	AG10803	skin:	n/a
24	chr1:120143242-120143292	NHDF-neo	bronchial:	n/a
25	chr1:120143242-120143292	HAEpiC	amniotic membrane:	n/a
26	chr1:120143242-120143292	HRCEpiC	kidney:	n/a
27	chr1:120143242-120143292	HMEC	breast:	n/a
28	chr1:120143242-120143292	MCF-7	breast:	n/a
29	chr1:120143242-120143292	GM06990	blood:	n/a
30	chr1:120143242-120143292	HNPCEpiC	eye:	n/a
31	chr1:120143242-120143292	HEK293	kidney:	embryo
32	chr1:120143242-120143292	BE2_C	brain:	n/a
33	chr1:120143242-120143292	NB4	blood:	n/a
34	chr1:120143242-120143292	SKMC	muscle:	n/a
35	chr1:120143242-120143292	Jurkat	blood:	n/a
36	chr1:120143242-120143292	ovcar-3	ovarian:	n/a
37	chr1:120143242-120143292	ECC-1	luminal epithelium:	n/a
38	chr1:120143242-120143292	SK-N-MC	brain:	n/a
39	chr1:120143242-120143292	A549	lung:	n/a
40	chr1:120143242-120143292	AoSMC	blood vessel:	n/a
41	chr1:120143242-120143292	HUVEC	blood vessel:	n/a
42	chr1:120143242-120143292	HRE	kidney:	n/a
43	chr1:120143242-120143292	K562	blood:	n/a
44	chr1:120143242-120143292	HCPEpiC	choroid plexus:	n/a
45	chr1:120143242-120143292	HEEpiC	esophagus:	n/a
46	chr1:120143242-120143292	HRPEpiC	eye:	n/a
47	chr1:120143242-120143292	PrEC	prostate:	n/a
48	chr1:120143242-120143292	U87	brain:	n/a
49	chr1:120143242-120143292	GM12891	blood:	n/a
50	chr1:120143242-120143292	NT2-D1	testis:	n/a

No.	Distal block	Cell Line	Cell type
1	chr1:120125219..120126121-chr1:120153919..120154547,2	MCF-7	breast:
2	chr1:119914912..119915700-chr1:120154301..120154847,3	MCF-7	breast:
3	chr1:120145059..120147660-chr1:120162749..120165475,2	MCF-7	breast:
4	chr1:120153476..120155640-chr1:120190161..120192811,2	K562	blood:
5	chr1:120091982..120092921-chr1:120150180..120150935,3	MCF-7	breast:
6	chr1:120154324..120155309-chr1:120205532..120206464,6	MCF-7	breast:
7	chr1:120125200..120126107-chr1:120217588..120218409,3	K562	blood:
8	chr1:120154003..120154965-chr1:120217033..120218809,10	K562	blood:
9	chr1:120125219..120126121-chr1:120153919..120154547,2	MCF-7	breast:
10	chr1:120154194..120154867-chr1:120205886..120206437,3	MCF-7	breast:
11	chr1:120154024..120154620-chr1:120217678..120218364,2	MCF-7	breast:
12	chr1:120154067..120155007-chr1:120217498..120218673,7	MCF-7	breast:
13	chr1:120153709..120155634-chr1:120202418..120204087,2	MCF-7	breast:
14	chr1:120154731..120156704-chr1:120158612..120160451,2	MCF-7	breast:
15	chr1:120151431..120154337-chr1:120190081..120192940,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PHGDH-1	chr1:120143780-120144107	ENSG00000242959.1
2	lnc-PHGDH-1	chr1:120144910-120145118	ENSG00000242959.1
3	lnc-ZNF697-3	chr1:120148999-120149695	NONHSAT005569
4	lnc-ZNF697-1	chr1:120140325-120141894	ENSG00000260941.1
5	lnc-ZNF697-1	chr1:120140325-120141914	NONHSAT005570

Variant related genes	Relation type
LINC00622	TF binding region
GAPDHP33	TF binding region
HSD3BP5	TF binding region
LINC00622	CpG island
GAPDHP33	CpG island
HSD3BP5	CpG island
ENSG00000143067	chromatin interactions
ENSG00000092621	chromatin interactions

Extended variants
information (count: 1353 )
Associated
traits (count: 88 )

Variant overlapped rSNPs/rCNVs (count:1353 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs587654226	chr1:120123727-120123728	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs587689033	chr1:120123730-120123731	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs587737442	chr1:120123731-120123732	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs587774957	chr1:120123732-120123733	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs112409240	chr1:120123735-120123736	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs433221	chr1:120123757-120123758	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs183257359	chr1:120123758-120123759	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs587767500	chr1:120123782-120123783	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs115382846	chr1:120123799-120123800	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs401992	chr1:120123801-120123802	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs373563	chr1:120123808-120123809	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs587635344	chr1:120123823-120123824	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs587644264	chr1:120123828-120123829	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs12133850	chr1:120123858-120123859	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs451402	chr1:120123903-120123904	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs10923865	chr1:120123911-120123912	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs116331778	chr1:120123925-120123926	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs148463572	chr1:120123935-120123936	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs370087464	chr1:120123949-120123950	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs587658618	chr1:120123981-120123982	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs587734077	chr1:120123987-120123988	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs12144062	chr1:120123990-120123991	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs187914384	chr1:120124014-120124015	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs146477255	chr1:120124026-120124027	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs587628506	chr1:120124027-120124028	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs587685910	chr1:120124030-120124031	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs416713	chr1:120124032-120124033	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs386635124	chr1:120124052-120124053	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs35548541	chr1:120124053-120124054	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs587688153	chr1:120124065-120124066	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs10923866	chr1:120124096-120124097	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs140436619	chr1:120124098-120124099	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs191325155	chr1:120124159-120124160	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs12085010	chr1:120124160-120124161	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs138339104	chr1:120124218-120124219	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs587725411	chr1:120124293-120124294	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs184540254	chr1:120124304-120124305	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs587630806	chr1:120124334-120124335	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs587716883	chr1:120124346-120124347	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs7551417	chr1:120124350-120124351	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs587672635	chr1:120124352-120124353	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs384080	chr1:120124364-120124365	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs189316408	chr1:120124420-120124421	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs192870174	chr1:120124436-120124437	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs587734584	chr1:120124449-120124450	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs7537698	chr1:120124466-120124467	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs587683328	chr1:120124469-120124470	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs184964426	chr1:120124480-120124481	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs587614886	chr1:120124502-120124503	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs111711945	chr1:120124509-120124510	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:88)

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
Breast cancer	21364760	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
Pancreatic endocrine tumor	17639061	CNVD
small cell lung cancer	20016488	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
Cancer	20164920	CNVD
Cancer	21272361	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:350 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:120111800-120129800	Weak transcription	Left Ventricle	heart
2	chr1:120112000-120129600	Weak transcription	Right Atrium	heart
3	chr1:120115200-120160800	Weak transcription	Gastric	stomach
4	chr1:120117000-120128200	Weak transcription	Placenta	Placenta
5	chr1:120117000-120128600	Weak transcription	Spleen	Spleen
6	chr1:120117400-120125400	Weak transcription	Primary monocytes fromperipheralblood	blood
7	chr1:120122000-120129000	Weak transcription	Ovary	ovary
8	chr1:120123000-120123800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr1:120123200-120123800	Enhancers	iPS-15b Cell Line	embryonic stem cell
10	chr1:120123600-120125400	Weak transcription	Monocytes-CD14+_RO01746	blood
11	chr1:120123800-120125200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
12	chr1:120123800-120128200	Weak transcription	Fetal Intestine Small	intestine
13	chr1:120125400-120125600	Enhancers	iPS-15b Cell Line	embryonic stem cell
14	chr1:120125400-120125600	Bivalent Enhancer	HSMMtube	muscle
15	chr1:120125400-120126000	Enhancers	Primary monocytes fromperipheralblood	blood
16	chr1:120125400-120128200	Enhancers	Monocytes-CD14+_RO01746	blood
17	chr1:120125600-120126200	Enhancers	Fetal Stomach	stomach
18	chr1:120125600-120126400	Enhancers	Fetal Lung	lung
19	chr1:120125600-120126800	Enhancers	Fetal Muscle Leg	muscle
20	chr1:120125800-120126000	Enhancers	Primary hematopoietic stem cells short term culture	blood
21	chr1:120126000-120128000	Weak transcription	Primary monocytes fromperipheralblood	blood
22	chr1:120126400-120130000	Weak transcription	Fetal Lung	lung
23	chr1:120126800-120127200	Weak transcription	Fetal Muscle Leg	muscle
24	chr1:120127200-120127400	Enhancers	Fetal Muscle Leg	muscle
25	chr1:120127400-120128600	Weak transcription	Fetal Muscle Leg	muscle
26	chr1:120128000-120129000	Enhancers	Primary monocytes fromperipheralblood	blood
27	chr1:120128000-120129000	Enhancers	Rectal Mucosa Donor 31	rectum
28	chr1:120128200-120128400	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
29	chr1:120128200-120128800	Enhancers	Primary hematopoietic stem cells short term culture	blood
30	chr1:120128200-120128800	Enhancers	Placenta	Placenta
31	chr1:120128200-120129000	Enhancers	Duodenum Mucosa	Duodenum
32	chr1:120128200-120129000	Enhancers	Fetal Intestine Small	intestine
33	chr1:120128200-120131000	Enhancers	Fetal Intestine Large	intestine
34	chr1:120128400-120128600	Enhancers	Monocytes-CD14+_RO01746	blood
35	chr1:120128600-120128800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
36	chr1:120128600-120128800	Enhancers	Fetal Muscle Leg	muscle
37	chr1:120128600-120128800	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
38	chr1:120128600-120129400	Enhancers	Spleen	Spleen
39	chr1:120128800-120129000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
40	chr1:120128800-120129200	Enhancers	Fetal Kidney	kidney
41	chr1:120128800-120129200	Weak transcription	Fetal Muscle Leg	muscle
42	chr1:120128800-120129600	Enhancers	Monocytes-CD14+_RO01746	blood
43	chr1:120128800-120129800	Weak transcription	Placenta	Placenta
44	chr1:120129000-120129400	Bivalent Enhancer	HSMM	muscle
45	chr1:120129000-120129600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
46	chr1:120129000-120129600	Enhancers	Lung	lung
47	chr1:120129000-120130200	Enhancers	Ovary	ovary
48	chr1:120129000-120131000	Enhancers	Breast Myoepithelial Primary Cells	Breast
49	chr1:120129000-120132600	Weak transcription	Primary monocytes fromperipheralblood	blood
50	chr1:120129000-120132800	Weak transcription	Fetal Intestine Small	intestine

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