Variant report

Variant	esv3399078
Chromosome Location	chr1:240126875-240188660
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	ARID3A	chr1:240150588-240150665	K562	blood:	n/a	n/a
2	BATF	chr1:240163956-240164183	GM12878	blood:	n/a	chr1:240164080-240164091
3	BHLHE40	chr1:240139682-240139994	GM12878	blood:	n/a	chr1:240139848-240139861
4	BHLHE40	chr1:240167580-240167631	K562	blood:	n/a	n/a
5	BHLHE40	chr1:240139793-240139993	HepG2	liver:	n/a	chr1:240139848-240139861
6	BRCA1	chr1:240166916-240166985	Hela-S3	cervix:	n/a	n/a
7	CBX3	chr1:240142815-240143131	K562	blood:	n/a	n/a
8	CEBPB	chr1:240163996-240164285	Hela-S3	cervix:	n/a	n/a
9	CEBPB	chr1:240186448-240186532	A549	lung:	n/a	n/a
10	CEBPB	chr1:240169259-240169362	A549	lung:	n/a	n/a
11	CEBPB	chr1:240163987-240164361	IMR90	lung:	n/a	n/a
12	CEBPB	chr1:240144058-240144074	HepG2	liver:	n/a	n/a
13	CEBPB	chr1:240163983-240164417	A549	lung:	n/a	n/a
14	CEBPB	chr1:240162605-240162639	A549	lung:	n/a	n/a
15	CREB1	chr1:240161146-240161378	A549	lung:	n/a	n/a
16	CTCF	chr1:240139800-240139950	Caco-2	colon:	n/a	chr1:240139838-240139848 chr1:240139835-240139853 chr1:240139841-240139850 chr1:240139837-240139850 chr1:240139830-240139851 chr1:240139836-240139852
17	CTCF	chr1:240174520-240174670	HVMF	connective:	n/a	n/a
18	CTCF	chr1:240161000-240161150	AG04450	lung:	n/a	n/a
19	CTCF	chr1:240167520-240167670	SAEC	small airway:	n/a	chr1:240167599-240167609 chr1:240167602-240167611 chr1:240167597-240167613 chr1:240167596-240167614 chr1:240167598-240167611 chr1:240167591-240167612
20	CTCF	chr1:240150457-240150728	K562	blood:	n/a	chr1:240150633-240150649 chr1:240150638-240150647 chr1:240150632-240150650 chr1:240150627-240150648 chr1:240150635-240150645 chr1:240150634-240150647
21	CTCF	chr1:240139633-240140060	GM12878	blood:	n/a	chr1:240139838-240139848 chr1:240139835-240139853 chr1:240139841-240139850 chr1:240139837-240139850 chr1:240139830-240139851 chr1:240139836-240139852
22	CTCF	chr1:240140120-240140270	NB4	blood:	n/a	n/a
23	CTCF	chr1:240161200-240161350	WI-38	lung:	n/a	chr1:240161291-240161304 chr1:240161295-240161304 chr1:240161289-240161307
24	CTCF	chr1:240167507-240167697	MCF-7	breast:	n/a	chr1:240167599-240167609 chr1:240167602-240167611 chr1:240167597-240167613 chr1:240167596-240167614 chr1:240167598-240167611 chr1:240167591-240167612
25	CTCF	chr1:240139120-240139270	AoAF	blood vessel:	n/a	n/a
26	CTCF	chr1:240139624-240140064	MCF-7	breast:	n/a	chr1:240139838-240139848 chr1:240139835-240139853 chr1:240139841-240139850 chr1:240139837-240139850 chr1:240139830-240139851 chr1:240139836-240139852
27	CTCF	chr1:240139760-240139910	HMF	breast:	n/a	chr1:240139838-240139848 chr1:240139835-240139853 chr1:240139841-240139850 chr1:240139837-240139850 chr1:240139830-240139851 chr1:240139836-240139852
28	CTCF	chr1:240174640-240174790	WERI-Rb-1	eye:	n/a	n/a
29	CTCF	chr1:240139780-240139930	NHDF-neo	bronchial:	n/a	chr1:240139838-240139848 chr1:240139835-240139853 chr1:240139841-240139850 chr1:240139837-240139850 chr1:240139830-240139851 chr1:240139836-240139852
30	CTCF	chr1:240169678-240169770	Medullo	brain:	n/a	n/a
31	CTCF	chr1:240168760-240168910	AG09309	skin:	n/a	chr1:240168775-240168796 chr1:240168780-240168798
32	CTCF	chr1:240161220-240161370	HFF-Myc	foreskin:	n/a	chr1:240161291-240161304 chr1:240161295-240161304 chr1:240161289-240161307
33	CTCF	chr1:240171820-240171970	WERI-Rb-1	eye:	n/a	n/a
34	CTCF	chr1:240169600-240169750	WERI-Rb-1	eye:	n/a	n/a
35	CTCF	chr1:240139731-240139989	MCF-7	breast:	n/a	chr1:240139838-240139848 chr1:240139835-240139853 chr1:240139841-240139850 chr1:240139837-240139850 chr1:240139830-240139851 chr1:240139836-240139852
36	CTCF	chr1:240167860-240168010	GM12872	blood:	n/a	n/a
37	CTCF	chr1:240150556-240150754	GM13977	blood:	n/a	chr1:240150633-240150649 chr1:240150638-240150647 chr1:240150632-240150650 chr1:240150627-240150648 chr1:240150635-240150645 chr1:240150634-240150647
38	CTCF	chr1:240150600-240150750	SAEC	small airway:	n/a	chr1:240150633-240150649 chr1:240150638-240150647 chr1:240150632-240150650 chr1:240150627-240150648 chr1:240150635-240150645 chr1:240150634-240150647
39	CTCF	chr1:240150453-240150724	SK-N-SH_RA	brain:	n/a	chr1:240150633-240150649 chr1:240150638-240150647 chr1:240150632-240150650 chr1:240150627-240150648 chr1:240150635-240150645 chr1:240150634-240150647
40	CTCF	chr1:240168643-240168926	IMR90	lung:	n/a	chr1:240168775-240168796 chr1:240168780-240168798
41	CTCF	chr1:240167520-240167670	A549	lung:	n/a	chr1:240167599-240167609 chr1:240167602-240167611 chr1:240167597-240167613 chr1:240167596-240167614 chr1:240167598-240167611 chr1:240167591-240167612
42	CTCF	chr1:240150560-240150710	HA-sp	spinal cord:	n/a	chr1:240150633-240150649 chr1:240150638-240150647 chr1:240150632-240150650 chr1:240150627-240150648 chr1:240150635-240150645 chr1:240150634-240150647
43	CTCF	chr1:240140115-240140193	GM19239	blood:	n/a	n/a
44	CTCF	chr1:240167520-240167670	HEEpiC	esophagus:	n/a	chr1:240167599-240167609 chr1:240167602-240167611 chr1:240167597-240167613 chr1:240167596-240167614 chr1:240167598-240167611 chr1:240167591-240167612
45	CTCF	chr1:240150560-240150710	GM12873	blood:	n/a	chr1:240150633-240150649 chr1:240150638-240150647 chr1:240150632-240150650 chr1:240150627-240150648 chr1:240150635-240150645 chr1:240150634-240150647
46	CTCF	chr1:240168760-240168910	HCPEpiC	choroid plexus:	n/a	chr1:240168775-240168796 chr1:240168780-240168798
47	CTCF	chr1:240150303-240151005	A549	lung:	n/a	chr1:240150633-240150649 chr1:240150638-240150647 chr1:240150632-240150650 chr1:240150627-240150648 chr1:240150635-240150645 chr1:240150634-240150647
48	CTCF	chr1:240168680-240168830	GM12873	blood:	n/a	chr1:240168775-240168796 chr1:240168780-240168798
49	CTCF	chr1:240139780-240139930	SK-N-SH_RA	brain:	n/a	chr1:240139838-240139848 chr1:240139835-240139853 chr1:240139841-240139850 chr1:240139837-240139850 chr1:240139830-240139851 chr1:240139836-240139852
50	CTCF	chr1:240167860-240168010	AG04449	skin:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:240161445-240161495	GM12878	blood:	n/a
2	chr1:240161445-240161495	GM12878	blood:	n/a
3	chr1:240161445-240161495	HPAEpiC	pulmonary alveolar:	n/a
4	chr1:240157611-240157661	NB4	blood:	n/a
5	chr1:240161445-240161495	HRPEpiC	eye:	n/a
6	chr1:240160972-240161022	AG04449	skin:	fetal
7	chr1:240160972-240161022	CMK	blood:	n/a
8	chr1:240161061-240161111	ovcar-3	ovarian:	n/a
9	chr1:240164755-240164805	ProgFib	skin:	n/a
10	chr1:240159816-240159866	AoSMC	blood vessel:	n/a
11	chr1:240159816-240159866	AG09309	skin:	n/a
12	chr1:240164755-240164805	ovcar-3	ovarian:	n/a
13	chr1:240161445-240161495	AG09309	skin:	n/a
14	chr1:240161061-240161111	HIPEpiC	eye:	n/a
15	chr1:240159816-240159866	Caco-2	colon:	n/a
16	chr1:240157611-240157661	GM06990	blood:	n/a
17	chr1:240161447-240161497	HL-60	blood:	n/a
18	chr1:240161249-240161299	GM19239	blood:	n/a
19	chr1:240160972-240161022	Hela-S3	cervix:	n/a
20	chr1:240161061-240161111	AoSMC	blood vessel:	n/a
21	chr1:240161447-240161497	ovcar-3	ovarian:	n/a
22	chr1:240161447-240161497	HCT-116	colon:	n/a
23	chr1:240161249-240161299	NHBE	bronchial:	n/a
24	chr1:240160972-240161022	HCT-116	colon:	n/a
25	chr1:240161445-240161495	SK-N-SH	brain:	n/a
26	chr1:240161249-240161299	AoSMC	blood vessel:	n/a
27	chr1:240164755-240164805	HL-60	blood:	n/a
28	chr1:240161445-240161495	GM06990	blood:	n/a
29	chr1:240159816-240159866	NHBE	bronchial:	n/a
30	chr1:240159816-240159866	HEK293	kidney:	embryo
31	chr1:240161445-240161495	HCM	heart:	n/a
32	chr1:240159816-240159866	SKMC	muscle:	n/a
33	chr1:240157611-240157661	HIPEpiC	eye:	n/a
34	chr1:240164755-240164805	HMEC	breast:	n/a
35	chr1:240161445-240161495	ProgFib	skin:	n/a
36	chr1:240162334-240162384	IMR90	lung:	fetal
37	chr1:240161249-240161299	AG04450	lung:	fetal
38	chr1:240161249-240161299	NB4	blood:	n/a
39	chr1:240157611-240157661	SK-N-SH_RA	brain:	n/a
40	chr1:240162334-240162384	BJ	skin:	n/a
41	chr1:240164755-240164805	AG04450	lung:	fetal
42	chr1:240161447-240161497	H1-hESC	embryonic stem cell:	embryo
43	chr1:240160972-240161022	GM19239	blood:	n/a
44	chr1:240164755-240164805	Hepatocyte	liver:	n/a
45	chr1:240159816-240159866	NB4	blood:	n/a
46	chr1:240162334-240162384	MCF10A-Er-Src	breast:	n/a
47	chr1:240159816-240159866	HNPCEpiC	eye:	n/a
48	chr1:240161445-240161495	HAEpiC	amniotic membrane:	n/a
49	chr1:240164755-240164805	MCF-7	breast:	n/a
50	chr1:240161249-240161299	IMR90	lung:	fetal

No.	Distal block	Cell Line	Cell type
1	chr1:240120788..240123095-chr1:240126047..240128075,2	K562	blood:
2	chr1:240114459..240115474-chr1:240139313..240140289,6	MCF-7	breast:
3	chr1:239879435..239880119-chr1:240167119..240168101,2	K562	blood:
4	chr1:240114597..240115121-chr1:240140710..240141521,2	MCF-7	breast:
5	chr1:240114563..240115514-chr1:240150165..240151144,4	MCF-7	breast:
6	chr1:240125187..240126841-chr1:240129827..240131822,2	K562	blood:
7	chr1:240114519..240115550-chr1:240150441..240150998,3	MCF-7	breast:
8	chr1:240114585..240115493-chr1:240139314..240140288,4	K562	blood:
9	chr1:240166457..240167256-chr9:121965917..121966447,2	MCF-7	breast:
10	chr1:240114818..240115571-chr1:240140344..240141173,2	MCF-7	breast:
11	chr1:240114810..240116148-chr1:240139242..240140249,5	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FMN2-3	chr1:240175922-240176645	NONHSAT010488
2	lnc-FMN2-3	chr1:240170836-240171065	NONHSAT010487
3	lnc-FMN2-3	chr1:240175922-240176560	NR_036695
4	lnc-FMN2-3	chr1:240170824-240171137	NR_036695
5	lnc-FMN2-3	chr1:240175922-240176645	NONHSAT010487
6	lnc-FMN2-3	chr1:240170836-240171137	NONHSAT010488
7	lnc-FMN2-3	chr1:240175946-240176526	NONHSAT010489

Variant related genes	Relation type
FMN2	TF binding region
ENSG00000215805	TF binding region
RPS7P5	TF binding region
FMN2	CpG island
ENSG00000215805	CpG island
RPS7P5	CpG island

Extended variants
information (count: 1210 )
Associated
traits (count: 87 )

Variant overlapped rSNPs/rCNVs (count:1210 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs538072779	chr1:240131981-240131982	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs147487787	chr1:240131991-240131992	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs574797326	chr1:240132037-240132038	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs10926043	chr1:240132039-240132040	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs547289767	chr1:240132041-240132042	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs530008776	chr1:240132046-240132047	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs553793947	chr1:240132050-240132051	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs180712338	chr1:240132055-240132056	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs546304024	chr1:240132076-240132077	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs201722665	chr1:240132085-240132086	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs571901800	chr1:240132089-240132090	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs576446259	chr1:240132102-240132103	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs186499169	chr1:240132145-240132146	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs190941169	chr1:240132164-240132165	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs111711433	chr1:240132225-240132226	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs376058999	chr1:240132238-240132239	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs181703111	chr1:240132308-240132309	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs559419676	chr1:240132318-240132319	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs532599395	chr1:240133427-240133428	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs12077444	chr1:240133472-240133473	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs528136750	chr1:240133476-240133477	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs547590026	chr1:240133516-240133517	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs574858258	chr1:240134676-240134677	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs375861137	chr1:240134702-240134703	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs565007399	chr1:240134706-240134707	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs138999035	chr1:240134728-240134729	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs540186760	chr1:240134739-240134740	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs545585525	chr1:240134744-240134745	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs574548334	chr1:240135841-240135842	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs72762527	chr1:240135888-240135889	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs554706723	chr1:240135892-240135893	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs4233479	chr1:240135902-240135903	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs148770648	chr1:240135922-240135923	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs540563726	chr1:240135924-240135925	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs143857620	chr1:240135930-240135931	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs4659557	chr1:240135933-240135934	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs190048025	chr1:240135946-240135947	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs115767243	chr1:240135957-240135958	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs12133285	chr1:240135971-240135972	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs146397763	chr1:240135989-240135990	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs202099454	chr1:240135990-240135991	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs566538091	chr1:240136007-240136008	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs527615861	chr1:240136015-240136016	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs527744444	chr1:240136024-240136025	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs570695754	chr1:240136036-240136037	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs139775164	chr1:240136045-240136046	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs556157559	chr1:240136078-240136079	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs147182018	chr1:240136096-240136097	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs55925140	chr1:240136102-240136103	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs367973164	chr1:240136174-240136175	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:87)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Melanoma	18172304	CNVD
Rett syndrome	21593744	CNVD
Medulloblastoma	21979893	CNVD
Cancer	20164919	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
Non-small cell lung cancer	21044232	CNVD
Cervical cancer	21063398	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	20632083	CNVD
Endometrial cancer	22040021	CNVD
Ewing''s sarcoma	21437220	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	21264507	CNVD
Liposarcoma	21253554	CNVD
Multiple myeloma	21628407	CNVD
Cancer	16751803	CNVD
Prostate cancer	16705090	CNVD
Neuroblastoma	19435921	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16461572	CNVD
Intracranial tumor	16823260	CNVD
Medulloblastoma	18056178	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Colorectal cancer	16272173	CNVD
Breast cancer	17603634	CNVD
Neuroblastoma	21899760	CNVD
Breast cancer	21858162	CNVD
Non-small cell lung cancer	21385341	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Testicular germ cell tumor	18059402	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Breast cancer	21509527	CNVD
Urothelial carcinoma	21177765	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Chordoma	18071362	CNVD
T-cell lymphomas	19863542	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hepatocellular carcinoma	18803288	CNVD
Urothelial tumor	18831757	CNVD
Lung cancer	18438408	CNVD
Medulloblastoma	16783165	CNVD
Basal cell lymphoma	17170743	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Congenital abnormalities	21549014	CNVD
Developmental delay	21549014	CNVD
Mental retardation	21549014	CNVD
small cell lung cancer	20016488	CNVD
Cancer	20164920	CNVD
Cancer	17060936	CNVD
abnormal development	18461090	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Myxofibrosarcoma	16751306	CNVD
Non-small cell lung cancer	21829676	CNVD
Hepatocellular carcinoma	16750200	CNVD
Arrhythmogenic right ventricular cardiomyopathy	17576883	CNVD
Multiple myeloma	16616336	CNVD
Developmental delay	21147756	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:190 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:240135800-240137200	Enhancers	Fetal Muscle Leg	muscle
2	chr1:240137200-240138600	Weak transcription	Fetal Muscle Leg	muscle
3	chr1:240138000-240138200	Enhancers	Fetal Intestine Small	intestine
4	chr1:240138200-240138800	Weak transcription	Fetal Intestine Small	intestine
5	chr1:240138800-240139200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
6	chr1:240138800-240139600	Enhancers	Fetal Intestine Small	intestine
7	chr1:240139000-240139200	Enhancers	Fetal Muscle Leg	muscle
8	chr1:240139000-240139600	Enhancers	Fetal Intestine Large	intestine
9	chr1:240142200-240143400	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
10	chr1:240142800-240143600	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
11	chr1:240144600-240145400	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
12	chr1:240145400-240147200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
13	chr1:240156600-240156800	Enhancers	Fetal Brain Male	brain
14	chr1:240157400-240157800	Bivalent Enhancer	Fetal Brain Male	brain
15	chr1:240158800-240160600	Weak transcription	H9 Cell Line	embryonic stem cell
16	chr1:240159800-240160000	Bivalent Enhancer	Fetal Brain Female	brain
17	chr1:240160000-240160400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
18	chr1:240160400-240160600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
19	chr1:240160600-240160800	Flanking Active TSS	H9 Cell Line	embryonic stem cell
20	chr1:240160600-240160800	Flanking Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
21	chr1:240160600-240160800	Bivalent Enhancer	Primary hematopoietic stem cells	blood
22	chr1:240160600-240160800	Bivalent/Poised TSS	Cortex derived primary cultured neurospheres	brain
23	chr1:240160600-240160800	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin01	Skin
24	chr1:240160600-240160800	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin03	Skin
25	chr1:240160600-240160800	Bivalent Enhancer	Fetal Intestine Large	intestine
26	chr1:240160600-240160800	Bivalent Enhancer	Fetal Muscle Leg	muscle
27	chr1:240160600-240161000	Bivalent Enhancer	Placenta	Placenta
28	chr1:240160600-240161200	Active TSS	H1 Cell Line	embryonic stem cell
29	chr1:240160600-240161400	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
30	chr1:240160600-240161400	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
31	chr1:240160600-240161600	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
32	chr1:240160600-240161600	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
33	chr1:240160600-240161600	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin02	Skin
34	chr1:240160600-240161800	Bivalent/Poised TSS	HUES48 Cell Line	embryonic stem cell
35	chr1:240160600-240161800	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
36	chr1:240160600-240161800	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
37	chr1:240160600-240161800	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
38	chr1:240160600-240161800	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
39	chr1:240160600-240161800	Bivalent Enhancer	Primary T helper cells fromperipheralblood	blood
40	chr1:240160600-240161800	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Female	--
41	chr1:240160600-240161800	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Male	--
42	chr1:240160600-240161800	Bivalent/Poised TSS	Brain Germinal Matrix	brain
43	chr1:240160600-240161800	Bivalent/Poised TSS	HSMM	muscle
44	chr1:240160800-240161000	Bivalent/Poised TSS	Primary hematopoietic stem cells	blood
45	chr1:240160800-240161000	Flanking Bivalent TSS/Enh	Fetal Brain Female	brain
46	chr1:240160800-240161000	Bivalent Enhancer	Fetal Intestine Small	intestine
47	chr1:240160800-240161000	Flanking Bivalent TSS/Enh	Fetal Muscle Trunk	muscle
48	chr1:240160800-240161000	Bivalent/Poised TSS	Psoas Muscle	Psoas
49	chr1:240160800-240161200	Bivalent/Poised TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
50	chr1:240160800-240161200	Bivalent/Poised TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

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