Variant report

Variant	esv2422256
Chromosome Location	chr1:238441961-238647862
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	chr1:238509171-238509547	HepG2	liver:	n/a	n/a
2	ATF1	chr1:238615222-238615353	K562	blood:	n/a	n/a
3	BATF	chr1:238504382-238504631	GM12878	blood:	n/a	chr1:238504431-238504440 chr1:238504503-238504514 chr1:238504504-238504514 chr1:238504508-238504518
4	BHLHE40	chr1:238580496-238580582	GM12878	blood:	n/a	chr1:238580532-238580541 chr1:238580527-238580548 chr1:238580531-238580544
5	BRCA1	chr1:238511858-238511895	Hela-S3	cervix:	n/a	n/a
6	BRCA1	chr1:238476183-238476253	Hela-S3	cervix:	n/a	n/a
7	CEBPB	chr1:238631420-238631725	A549	lung:	n/a	chr1:238631602-238631613 chr1:238631489-238631501 chr1:238631562-238631573 chr1:238631561-238631574
8	CEBPB	chr1:238507207-238507403	H1-hESC	embryonic stem cell:	n/a	chr1:238507290-238507301
9	CEBPB	chr1:238500614-238500859	HepG2	liver:	n/a	n/a
10	CEBPB	chr1:238494877-238495212	A549	lung:	n/a	chr1:238495053-238495064
11	CEBPB	chr1:238494961-238495151	H1-hESC	embryonic stem cell:	n/a	chr1:238495053-238495064
12	CEBPB	chr1:238486789-238487155	HepG2	liver:	n/a	chr1:238486969-238486980 chr1:238486968-238486981 chr1:238486970-238486979 chr1:238486970-238486979 chr1:238486970-238486979
13	CEBPB	chr1:238494898-238495230	HepG2	liver:	n/a	chr1:238495053-238495064
14	CEBPB	chr1:238577659-238577940	HepG2	liver:	n/a	chr1:238577789-238577800
15	CEBPB	chr1:238569977-238570046	H1-hESC	embryonic stem cell:	n/a	n/a
16	CEBPB	chr1:238577638-238577960	IMR90	lung:	n/a	chr1:238577789-238577800
17	CEBPB	chr1:238568024-238568676	IMR90	lung:	n/a	chr1:238568324-238568335
18	CEBPB	chr1:238486776-238487130	H1-hESC	embryonic stem cell:	n/a	chr1:238486969-238486980 chr1:238486968-238486981 chr1:238486970-238486979 chr1:238486970-238486979 chr1:238486970-238486979
19	CEBPB	chr1:238615248-238615560	H1-hESC	embryonic stem cell:	n/a	chr1:238615411-238615420 chr1:238615411-238615420 chr1:238615409-238615422 chr1:238615408-238615425 chr1:238615410-238615421 chr1:238615411-238615420 chr1:238615409-238615422
20	CEBPB	chr1:238615243-238615583	HepG2	liver:	n/a	chr1:238615411-238615420 chr1:238615411-238615420 chr1:238615409-238615422 chr1:238615408-238615425 chr1:238615410-238615421 chr1:238615411-238615420 chr1:238615409-238615422
21	CEBPB	chr1:238615281-238615498	K562	blood:	n/a	chr1:238615411-238615420 chr1:238615411-238615420 chr1:238615409-238615422 chr1:238615408-238615425 chr1:238615410-238615421 chr1:238615411-238615420 chr1:238615409-238615422
22	CEBPB	chr1:238630757-238631088	HepG2	liver:	n/a	chr1:238630909-238630920
23	CEBPB	chr1:238494889-238495170	K562	blood:	n/a	chr1:238495053-238495064
24	CEBPB	chr1:238630755-238631065	IMR90	lung:	n/a	chr1:238630909-238630920
25	CEBPB	chr1:238486791-238487125	K562	blood:	n/a	chr1:238486969-238486980 chr1:238486968-238486981 chr1:238486970-238486979 chr1:238486970-238486979 chr1:238486970-238486979
26	CEBPB	chr1:238572844-238573071	HepG2	liver:	n/a	chr1:238572907-238572918
27	CEBPB	chr1:238494902-238495225	IMR90	lung:	n/a	chr1:238495053-238495064
28	CEBPB	chr1:238572449-238573112	IMR90	lung:	n/a	chr1:238572907-238572918
29	CEBPB	chr1:238568159-238568398	HepG2	liver:	n/a	chr1:238568324-238568335
30	CEBPB	chr1:238631412-238631746	HepG2	liver:	n/a	chr1:238631602-238631613 chr1:238631489-238631501 chr1:238631562-238631573 chr1:238631561-238631574
31	CEBPB	chr1:238559442-238559698	Hela-S3	cervix:	n/a	chr1:238559551-238559564 chr1:238559551-238559564 chr1:238559551-238559564 chr1:238559553-238559564 chr1:238559551-238559562 chr1:238559553-238559562
32	CEBPB	chr1:238486784-238487154	IMR90	lung:	n/a	chr1:238486969-238486980 chr1:238486968-238486981 chr1:238486970-238486979 chr1:238486970-238486979 chr1:238486970-238486979
33	CEBPB	chr1:238486692-238487151	A549	lung:	n/a	chr1:238486969-238486980 chr1:238486968-238486981 chr1:238486970-238486979 chr1:238486970-238486979 chr1:238486970-238486979
34	CEBPB	chr1:238507178-238507424	IMR90	lung:	n/a	chr1:238507290-238507301
35	CEBPB	chr1:238615272-238615512	Hela-S3	cervix:	n/a	chr1:238615411-238615420 chr1:238615411-238615420 chr1:238615409-238615422 chr1:238615408-238615425 chr1:238615410-238615421 chr1:238615411-238615420 chr1:238615409-238615422
36	CEBPB	chr1:238443126-238443326	HepG2	liver:	n/a	chr1:238443247-238443258
37	CEBPB	chr1:238621057-238621369	Hela-S3	cervix:	n/a	chr1:238621191-238621204
38	CEBPB	chr1:238615230-238615540	A549	lung:	n/a	chr1:238615411-238615420 chr1:238615411-238615420 chr1:238615409-238615422 chr1:238615408-238615425 chr1:238615410-238615421 chr1:238615411-238615420 chr1:238615409-238615422
39	CEBPB	chr1:238615224-238615590	IMR90	lung:	n/a	chr1:238615411-238615420 chr1:238615411-238615420 chr1:238615409-238615422 chr1:238615408-238615425 chr1:238615410-238615421 chr1:238615411-238615420 chr1:238615409-238615422
40	CEBPB	chr1:238486807-238487150	Hela-S3	cervix:	n/a	chr1:238486969-238486980 chr1:238486968-238486981 chr1:238486970-238486979 chr1:238486970-238486979 chr1:238486970-238486979
41	CEBPB	chr1:238507177-238507481	HepG2	liver:	n/a	chr1:238507290-238507301
42	CEBPB	chr1:238630792-238631073	A549	lung:	n/a	chr1:238630909-238630920
43	CEBPB	chr1:238613748-238613931	A549	lung:	n/a	chr1:238613831-238613842
44	CEBPB	chr1:238559415-238559707	HepG2	liver:	n/a	chr1:238559551-238559564 chr1:238559551-238559564 chr1:238559551-238559564 chr1:238559553-238559564 chr1:238559551-238559562 chr1:238559553-238559562
45	CEBPB	chr1:238577636-238577882	A549	lung:	n/a	chr1:238577789-238577800
46	CEBPB	chr1:238613716-238613944	HepG2	liver:	n/a	chr1:238613831-238613842
47	CTBP2	chr1:238540651-238541261	H1-hESC	embryonic stem cell:	n/a	n/a
48	CTCF	chr1:238565176-238565206	GM20000	blood:	n/a	n/a
49	CTCF	chr1:238593131-238593330	IMR90	lung:	n/a	n/a
50	CTCF	chr1:238563000-238563150	HPAF	blood vessel:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:238644629-238644679	SKMC	muscle:	n/a
2	chr1:238644629-238644679	HL-60	blood:	n/a
3	chr1:238540640-238540690	HEK293	kidney:	embryo
4	chr1:238490308-238490358	K562	blood:	n/a
5	chr1:238644629-238644679	AG10803	skin:	n/a
6	chr1:238644629-238644679	MCF-7	breast:	n/a
7	chr1:238644629-238644679	AG04450	lung:	fetal
8	chr1:238540640-238540690	HCF	heart:	n/a
9	chr1:238540640-238540690	HNPCEpiC	eye:	n/a
10	chr1:238490308-238490358	HAEpiC	amniotic membrane:	n/a
11	chr1:238490308-238490358	NT2-D1	testis:	n/a
12	chr1:238540640-238540690	BJ	skin:	n/a
13	chr1:238490308-238490358	ProgFib	skin:	n/a
14	chr1:238540640-238540690	MCF10A-Er-Src	breast:	n/a
15	chr1:238490308-238490358	H1-hESC	embryonic stem cell:	embryo
16	chr1:238490308-238490358	HCT-116	colon:	n/a
17	chr1:238490308-238490358	HNPCEpiC	eye:	n/a
18	chr1:238490308-238490358	Hela-S3	cervix:	n/a
19	chr1:238540640-238540690	CMK	blood:	n/a
20	chr1:238490308-238490358	MCF-7	breast:	n/a
21	chr1:238490308-238490358	BE2_C	brain:	n/a
22	chr1:238540640-238540690	ProgFib	skin:	n/a
23	chr1:238490308-238490358	ovcar-3	ovarian:	n/a
24	chr1:238644629-238644679	Hela-S3	cervix:	n/a
25	chr1:238490308-238490358	A549	lung:	n/a
26	chr1:238644629-238644679	HNPCEpiC	eye:	n/a
27	chr1:238490308-238490358	HRE	kidney:	n/a
28	chr1:238540640-238540690	Caco-2	colon:	n/a
29	chr1:238540640-238540690	AG09319	gingival:	n/a
30	chr1:238490308-238490358	T-47D	breast:	n/a
31	chr1:238644629-238644679	NB4	blood:	n/a
32	chr1:238490308-238490358	SK-N-SH_RA	brain:	n/a
33	chr1:238540640-238540690	AG04450	lung:	fetal
34	chr1:238644629-238644679	NHDF-neo	bronchial:	n/a
35	chr1:238540640-238540690	HUVEC	blood vessel:	n/a
36	chr1:238490308-238490358	NHBE	bronchial:	n/a
37	chr1:238644629-238644679	HCF	heart:	n/a
38	chr1:238644629-238644679	PrEC	prostate:	n/a
39	chr1:238644629-238644679	MCF10A-Er-Src	breast:	n/a
40	chr1:238490308-238490358	LNCaP	prostate:	n/a
41	chr1:238644629-238644679	SK-N-SH_RA	brain:	n/a
42	chr1:238490308-238490358	AG04450	lung:	fetal
43	chr1:238490308-238490358	PFSK-1	brain:	n/a
44	chr1:238644629-238644679	IMR90	lung:	fetal
45	chr1:238490308-238490358	GM12878	blood:	n/a
46	chr1:238644629-238644679	BJ	skin:	n/a
47	chr1:238644629-238644679	AG09309	skin:	n/a
48	chr1:238490308-238490358	IMR90	lung:	fetal
49	chr1:238490308-238490358	GM12892	blood:	n/a
50	chr1:238540640-238540690	Hepatocyte	liver:	n/a

No.	Distal block	Cell Line	Cell type
1	chr1:238569164..238571164-chr1:238574150..238576513,2	K562	blood:
2	chr1:238641252..238644236-chr1:238645567..238648167,2	K562	blood:
3	chr1:238641252..238644236-chr1:238645567..238648167,2	K562	blood:
4	chr1:238593632..238594527-chr4:152881866..152882771,2	MCF-7	breast:
5	chr1:238457966..238460007-chr1:238462730..238464980,2	K562	blood:
6	chr1:238610421..238612456-chr1:238615042..238617696,2	K562	blood:
7	chr1:238610421..238612456-chr1:238615042..238617696,2	K562	blood:
8	chr1:238616483..238619038-chr1:238620922..238622486,2	K562	blood:
9	chr1:238616483..238619038-chr1:238620922..238622486,2	K562	blood:
10	chr1:238493493..238495641-chr1:238497004..238499734,2	K562	blood:
11	chr1:238457966..238460007-chr1:238462730..238464980,2	K562	blood:
12	chr1:238493493..238495641-chr1:238497004..238499734,2	K562	blood:
13	chr1:238598149..238599649-chr14:35023585..35025811,2	MCF-7	breast:
14	chr1:238569164..238571164-chr1:238574150..238576513,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RYR2-6	chr1:238486383-238486508	NONHSAT010457
2	lnc-ZP4-1	chr1:238643684-238644981	NR_015407
3	lnc-RYR2-6	chr1:238535201-238535295	NONHSAT010457
4	lnc-RYR2-6	chr1:238489512-238489574	NONHSAT010457
5	lnc-ZP4-1	chr1:238643686-238644981	XLOC_001272
6	lnc-RYR2-6	chr1:238489065-238489133	NONHSAT010457
7	lnc-RYR2-2	chr1:238608036-238608261	XLOC_000635
8	lnc-RYR2-2	chr1:238588741-238588811	XLOC_000635
9	lnc-RYR2-1	chr1:238450243-238450316	ENSG00000234464
10	lnc-RYR2-1	chr1:238450243-238450316	NONHSAT010455

Variant related genes	Relation type
RNU6-725P	TF binding region
ENSG00000231877	TF binding region
RNU6-725P	CpG island
ENSG00000231877	CpG island
ENSG00000206588	chromatin interactions
ACTR8	miRNA target sites
ACTR1A	miRNA target sites

Extended variants
information (count: 6218 )
Associated
traits (count: 93 )

Variant overlapped rSNPs/rCNVs (count:6218 , 50 per page) page: 1 2 3 4 5 6 7 ... 125

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs184037181	chr1:238441981-238441982	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs559967500	chr1:238442023-238442024	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs557395008	chr1:238442060-238442061	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs551388937	chr1:238442253-238442254	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs569525739	chr1:238442357-238442358	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs259634	chr1:238442375-238442376	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs549062086	chr1:238442383-238442384	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs567475967	chr1:238442430-238442431	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs569322984	chr1:238442464-238442465	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs147479749	chr1:238442495-238442496	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs553011063	chr1:238442496-238442497	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs577903729	chr1:238442501-238442502	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs34086132	chr1:238442564-238442565	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs567440919	chr1:238442565-238442566	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs386370140	chr1:238442567-238442568	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs201326001	chr1:238442568-238442569	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs373247398	chr1:238442572-238442573	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs76862316	chr1:238442574-238442575	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs111547374	chr1:238442580-238442581	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs573713710	chr1:238442604-238442605	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs12094201	chr1:238442713-238442714	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs151310657	chr1:238442724-238442725	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs199582715	chr1:238442767-238442768	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs73116553	chr1:238442795-238442796	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs11799950	chr1:238444020-238444021	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs535157835	chr1:238444056-238444057	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs79471271	chr1:238444074-238444075	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs145015146	chr1:238444117-238444118	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs532409334	chr1:238444129-238444130	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs545239445	chr1:238444130-238444131	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs199986296	chr1:238444142-238444143	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs71567203	chr1:238444236-238444237	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs200137420	chr1:238444237-238444238	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs200652545	chr1:238444251-238444252	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs557575229	chr1:238444302-238444303	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs576036167	chr1:238444379-238444380	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs543341288	chr1:238444389-238444390	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs550556834	chr1:238444390-238444391	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs259637	chr1:238444393-238444394	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs374006818	chr1:238444395-238444396	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs572710394	chr1:238444432-238444433	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs540326117	chr1:238444452-238444453	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs564800916	chr1:238444510-238444511	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs144738998	chr1:238444511-238444512	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs184786992	chr1:238444549-238444550	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs562318327	chr1:238444565-238444566	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs189155997	chr1:238444566-238444567	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs548359040	chr1:238444578-238444579	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs146701086	chr1:238444589-238444590	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs564749673	chr1:238444595-238444596	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:93)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Autism	22495311	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
Prostate cancer	18632612	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
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Glioma	20126413	CNVD
early-passage human iPS cells	21368824	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:431 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:238441800-238442800	Weak transcription	Fetal Lung	lung
2	chr1:238444000-238444600	Enhancers	Fetal Lung	lung
3	chr1:238444800-238445400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
4	chr1:238451800-238452000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr1:238459000-238460800	Enhancers	Fetal Intestine Small	intestine
6	chr1:238469400-238469800	Enhancers	Primary hematopoietic stem cells short term culture	blood
7	chr1:238469400-238470200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
8	chr1:238481400-238483600	Enhancers	Liver	Liver
9	chr1:238481800-238482200	Enhancers	Duodenum Mucosa	Duodenum
10	chr1:238481800-238482200	Enhancers	Fetal Intestine Small	intestine
11	chr1:238483200-238483600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
12	chr1:238483200-238483800	Enhancers	HMEC	breast
13	chr1:238483400-238483800	Enhancers	NHEK	skin
14	chr1:238486200-238486800	Enhancers	Stomach Mucosa	stomach
15	chr1:238486600-238488000	Enhancers	Fetal Intestine Small	intestine
16	chr1:238486800-238487400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
17	chr1:238486800-238487400	Weak transcription	Stomach Mucosa	stomach
18	chr1:238487000-238489000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
19	chr1:238487200-238488800	Enhancers	Primary hematopoietic stem cells short term culture	blood
20	chr1:238487200-238489000	Enhancers	Primary hematopoietic stem cells	blood
21	chr1:238487400-238487600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
22	chr1:238487400-238488200	Enhancers	Stomach Mucosa	stomach
23	chr1:238487600-238487800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
24	chr1:238487600-238488200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
25	chr1:238487800-238488000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
26	chr1:238488000-238488200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
27	chr1:238488000-238488800	Enhancers	HSMMtube	muscle
28	chr1:238488200-238493000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
29	chr1:238488200-238494400	Weak transcription	Stomach Mucosa	stomach
30	chr1:238488800-238493600	Weak transcription	HSMMtube	muscle
31	chr1:238489000-238492800	Weak transcription	Primary hematopoietic stem cells	blood
32	chr1:238492400-238492800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
33	chr1:238492600-238495600	Enhancers	Primary monocytes fromperipheralblood	blood
34	chr1:238492800-238493400	Enhancers	Primary hematopoietic stem cells	blood
35	chr1:238492800-238518000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
36	chr1:238493000-238493200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
37	chr1:238493000-238493400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
38	chr1:238493000-238494000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
39	chr1:238493000-238495400	Enhancers	Primary hematopoietic stem cells short term culture	blood
40	chr1:238493000-238495400	Enhancers	Small Intestine	intestine
41	chr1:238493200-238494000	Enhancers	Monocytes-CD14+_RO01746	blood
42	chr1:238493200-238494800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
43	chr1:238493400-238493800	Flanking Active TSS	Primary hematopoietic stem cells	blood
44	chr1:238493400-238494000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
45	chr1:238493600-238494000	Enhancers	HSMMtube	muscle
46	chr1:238493800-238494000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
47	chr1:238493800-238495000	Enhancers	Osteobl	bone
48	chr1:238494000-238494400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
49	chr1:238494000-238494400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
50	chr1:238494000-238501400	Weak transcription	Monocytes-CD14+_RO01746	blood

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