Variant report

Variant	esv16231
Chromosome Location	chr1:224204343-224241314
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	chr1:224238520-224238874	K562	blood:	n/a	n/a
2	ARID3A	chr1:224238457-224238876	HepG2	liver:	n/a	n/a
3	ARID3A	chr1:224225266-224225295	K562	blood:	n/a	n/a
4	BACH1	chr1:224238693-224238782	K562	blood:	n/a	n/a
5	BATF	chr1:224216986-224217637	GM12878	blood:	n/a	n/a
6	BATF	chr1:224216980-224217656	GM12878	blood:	n/a	n/a
7	BATF	chr1:224220653-224220945	GM12878	blood:	n/a	chr1:224220777-224220788
8	BATF	chr1:224220613-224220910	GM12878	blood:	n/a	chr1:224220777-224220788
9	BATF	chr1:224223656-224223852	GM12878	blood:	n/a	chr1:224223690-224223700
10	BCL11A	chr1:224217248-224217715	GM12878	blood:	n/a	chr1:224217512-224217521
11	BCL11A	chr1:224217376-224217584	GM12878	blood:	n/a	chr1:224217512-224217521
12	BHLHE40	chr1:224238699-224238742	K562	blood:	n/a	n/a
13	CBX3	chr1:224224984-224225484	K562	blood:	n/a	n/a
14	CEBPB	chr1:224225448-224225623	A549	lung:	n/a	n/a
15	CEBPB	chr1:224240694-224240740	IMR90	lung:	n/a	n/a
16	CEBPB	chr1:224239638-224239872	K562	blood:	n/a	chr1:224239704-224239715
17	CEBPB	chr1:224225002-224225648	K562	blood:	n/a	n/a
18	CEBPB	chr1:224217332-224217575	K562	blood:	n/a	n/a
19	CEBPB	chr1:224225413-224225664	K562	blood:	n/a	n/a
20	CEBPB	chr1:224238785-224238817	K562	blood:	n/a	n/a
21	CEBPB	chr1:224239683-224239843	H1-hESC	embryonic stem cell:	n/a	chr1:224239704-224239715
22	CEBPB	chr1:224239670-224239870	HepG2	liver:	n/a	chr1:224239704-224239715
23	CEBPB	chr1:224225438-224225638	IMR90	lung:	n/a	n/a
24	CEBPB	chr1:224225457-224225635	HepG2	liver:	n/a	n/a
25	CEBPB	chr1:224225290-224225590	K562	blood:	n/a	n/a
26	CEBPB	chr1:224239576-224239905	MCF-7	breast:	n/a	chr1:224239704-224239715
27	CEBPD	chr1:224225005-224225370	K562	blood:	n/a	n/a
28	CTCF	chr1:224238640-224238790	GM12878	blood:	n/a	chr1:224238693-224238711 chr1:224238699-224238708 chr1:224238696-224238706
29	CTCF	chr1:224238620-224238770	GM12878	blood:	n/a	chr1:224238693-224238711 chr1:224238699-224238708 chr1:224238696-224238706
30	CTCF	chr1:224238558-224238822	HepG2	liver:	n/a	chr1:224238693-224238711 chr1:224238699-224238708 chr1:224238696-224238706
31	CTCF	chr1:224238584-224238796	A549	lung:	n/a	chr1:224238693-224238711 chr1:224238699-224238708 chr1:224238696-224238706
32	CTCF	chr1:224238541-224238894	T-47D	breast:	n/a	chr1:224238693-224238711 chr1:224238699-224238708 chr1:224238696-224238706
33	CTCF	chr1:224238660-224238810	HPF	lung:	n/a	chr1:224238693-224238711 chr1:224238699-224238708 chr1:224238696-224238706
34	CTCF	chr1:224238560-224238710	NHEK	skin:	n/a	chr1:224238699-224238708 chr1:224238696-224238706
35	CTCF	chr1:224205454-224205483	GM13976	blood:	n/a	n/a
36	CTCF	chr1:224238660-224238810	HPAF	blood vessel:	n/a	chr1:224238693-224238711 chr1:224238699-224238708 chr1:224238696-224238706
37	CTCF	chr1:224206440-224206590	Hela-S3	cervix:	n/a	n/a
38	CTCF	chr1:224238620-224238770	HUVEC	blood vessel:	n/a	chr1:224238693-224238711 chr1:224238699-224238708 chr1:224238696-224238706
39	CTCF	chr1:224238573-224238841	Spleen_OC	spleen:	n/a	chr1:224238693-224238711 chr1:224238699-224238708 chr1:224238696-224238706
40	CTCF	chr1:224238620-224238770	HA-sp	spinal cord:	n/a	chr1:224238693-224238711 chr1:224238699-224238708 chr1:224238696-224238706
41	CTCF	chr1:224207704-224207733	GM10248	blood:	n/a	n/a
42	CTCF	chr1:224238640-224238790	GM12871	blood:	n/a	chr1:224238693-224238711 chr1:224238699-224238708 chr1:224238696-224238706
43	CTCF	chr1:224238640-224238790	AG09319	gingival:	n/a	chr1:224238693-224238711 chr1:224238699-224238708 chr1:224238696-224238706
44	CTCF	chr1:224238364-224238929	HCT-116	colon:	n/a	chr1:224238693-224238711 chr1:224238699-224238708 chr1:224238696-224238706
45	CTCF	chr1:224238589-224238798	GM13976	blood:	n/a	chr1:224238693-224238711 chr1:224238699-224238708 chr1:224238696-224238706
46	CTCF	chr1:224239020-224239170	GM12875	blood:	n/a	n/a
47	CTCF	chr1:224238590-224238829	GM10248	blood:	n/a	chr1:224238693-224238711 chr1:224238699-224238708 chr1:224238696-224238706
48	CTCF	chr1:224238640-224238790	HUVEC	blood vessel:	n/a	chr1:224238693-224238711 chr1:224238699-224238708 chr1:224238696-224238706
49	CTCF	chr1:224238640-224238790	HEEpiC	esophagus:	n/a	chr1:224238693-224238711 chr1:224238699-224238708 chr1:224238696-224238706
50	CTCF	chr1:224238620-224238770	GM12871	blood:	n/a	chr1:224238693-224238711 chr1:224238699-224238708 chr1:224238696-224238706

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:224224049-224224099	HCM	heart:	n/a
2	chr1:224224049-224224099	AG09319	gingival:	n/a
3	chr1:224222745-224222795	PFSK-1	brain:	n/a
4	chr1:224222745-224222795	HAEpiC	amniotic membrane:	n/a
5	chr1:224224049-224224099	SK-N-SH	brain:	n/a
6	chr1:224222745-224222795	HIPEpiC	eye:	n/a
7	chr1:224222745-224222795	AG04450	lung:	fetal
8	chr1:224224049-224224099	ovcar-3	ovarian:	n/a
9	chr1:224224049-224224099	Hepatocyte	liver:	n/a
10	chr1:224222745-224222795	HUVEC	blood vessel:	n/a
11	chr1:224222745-224222795	SK-N-SH	brain:	n/a
12	chr1:224224049-224224099	CMK	blood:	n/a
13	chr1:224224049-224224099	HPAEpiC	pulmonary alveolar:	n/a
14	chr1:224222745-224222795	HEK293	kidney:	embryo
15	chr1:224222745-224222795	IMR90	lung:	fetal
16	chr1:224224049-224224099	NB4	blood:	n/a
17	chr1:224222745-224222795	GM06990	blood:	n/a
18	chr1:224222745-224222795	HRE	kidney:	n/a
19	chr1:224222745-224222795	NH-A	brain:	n/a
20	chr1:224224049-224224099	NHDF-neo	bronchial:	n/a
21	chr1:224224049-224224099	GM19239	blood:	n/a
22	chr1:224222745-224222795	BJ	skin:	n/a
23	chr1:224224049-224224099	GM12892	blood:	n/a
24	chr1:224224049-224224099	HRCEpiC	kidney:	n/a
25	chr1:224224049-224224099	HCPEpiC	choroid plexus:	n/a
26	chr1:224222745-224222795	AG09319	gingival:	n/a
27	chr1:224224049-224224099	HAEpiC	amniotic membrane:	n/a
28	chr1:224224049-224224099	PrEC	prostate:	n/a
29	chr1:224224049-224224099	T-47D	breast:	n/a
30	chr1:224222745-224222795	NB4	blood:	n/a
31	chr1:224222745-224222795	HRCEpiC	kidney:	n/a
32	chr1:224224049-224224099	NT2-D1	testis:	n/a
33	chr1:224224049-224224099	SAEC	small airway:	n/a
34	chr1:224222745-224222795	Hepatocyte	liver:	n/a
35	chr1:224222745-224222795	SKMC	muscle:	n/a
36	chr1:224222745-224222795	LNCaP	prostate:	n/a
37	chr1:224222745-224222795	BE2_C	brain:	n/a
38	chr1:224222745-224222795	SK-N-SH_RA	brain:	n/a
39	chr1:224224049-224224099	MCF-7	breast:	n/a
40	chr1:224224049-224224099	U87	brain:	n/a
41	chr1:224224049-224224099	GM12878	blood:	n/a
42	chr1:224222745-224222795	H1-hESC	embryonic stem cell:	embryo
43	chr1:224222745-224222795	HL-60	blood:	n/a
44	chr1:224222745-224222795	MCF10A-Er-Src	breast:	n/a
45	chr1:224222745-224222795	Jurkat	blood:	n/a
46	chr1:224224049-224224099	K562	blood:	n/a
47	chr1:224222745-224222795	CMK	blood:	n/a
48	chr1:224222745-224222795	NHBE	bronchial:	n/a
49	chr1:224224049-224224099	RPTEC	kidney:	n/a
50	chr1:224222745-224222795	K562	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr1:224233477..224236319-chr1:224241343..224244947,3	K562	blood:
2	chr1:224240047..224241557-chr1:224249398..224251506,2	MCF-7	breast:
3	chr1:224232698..224234827-chr1:224235389..224237378,2	K562	blood:
4	chr1:223946751..223947655-chr1:224238232..224238830,2	K562	blood:
5	chr1:224238624..224240170-chr1:224243287..224246232,2	K562	blood:
6	chr1:224232698..224234827-chr1:224235389..224237378,2	K562	blood:
7	chr1:224240269..224242100-chr1:224243386..224246178,2	K562	blood:
8	chr1:224231878..224234198-chr1:224234605..224237378,2	K562	blood:
9	chr1:224237229..224240186-chr1:224247839..224250746,3	K562	blood:
10	chr1:224240818..224242542-chr1:224514996..224517845,2	K562	blood:
11	chr1:223882839..223883549-chr1:224238722..224239406,2	K562	blood:
12	chr1:223885668..223886563-chr1:224238061..224239140,4	K562	blood:
13	chr1:224233420..224235277-chr1:224246228..224248630,2	K562	blood:
14	chr1:224239914..224241769-chr1:224243528..224246178,2	K562	blood:
15	chr1:224237251..224240101-chr1:224270506..224273233,2	K562	blood:
16	chr1:224227960..224229471-chr1:224345929..224348019,2	K562	blood:
17	chr1:224231878..224234198-chr1:224234605..224237378,2	K562	blood:
18	chr1:224238230..224238917-chr1:224645015..224645671,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FBXO28-4	chr1:224217383-224217533	NONHSAT009768
2	lnc-FBXO28-4	chr1:224216253-224216275	NONHSAT009766
3	lnc-TP53BP2-7	chr1:224218406-224218498	NONHSAT009769
4	lnc-FBXO28-4	chr1:224216253-224216275	NONHSAT009767
5	lnc-TP53BP2-7	chr1:224222656-224222758	NONHSAT009769
6	lnc-FBXO28-4	chr1:224216529-224216829	NONHSAT009766
7	lnc-FBXO28-4	chr1:224219818-224220034	NONHSAT009766
8	lnc-TP53BP2-7	chr1:224221175-224221224	NONHSAT009769
9	lnc-FBXO28-4	chr1:224216529-224216829	NONHSAT009767
10	lnc-FBXO28-4	chr1:224216293-224216829	NONHSAT009768
11	lnc-FBXO28-4	chr1:224222257-224222380	NONHSAT009767

Variant related genes	Relation type
ENSG00000269358	TF binding region
ENSG00000229930	TF binding region
ENSG00000269358	CpG island
ENSG00000229930	CpG island
ENSG00000143748	chromatin interactions
ENSG00000162909	chromatin interactions

Extended variants
information (count: 1036 )
Associated
traits (count: 97 )

Variant overlapped rSNPs/rCNVs (count:1036 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs535482840	chr1:224204348-224204349	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs551255768	chr1:224204405-224204406	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs371834673	chr1:224204422-224204423	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs55731753	chr1:224204433-224204434	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs527354004	chr1:224204464-224204465	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs548673393	chr1:224204635-224204636	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs566921446	chr1:224204679-224204680	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs537490816	chr1:224204682-224204683	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs556427527	chr1:224204684-224204685	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs199745278	chr1:224204761-224204762	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs539341192	chr1:224204806-224204807	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs551826300	chr1:224204832-224204833	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs113672801	chr1:224204838-224204839	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs184221758	chr1:224204855-224204856	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs542750862	chr1:224204874-224204875	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs2995588	chr1:224204886-224204887	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs374300886	chr1:224204905-224204906	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs576490031	chr1:224204907-224204908	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs543865547	chr1:224204931-224204932	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs2995587	chr1:224204934-224204935	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs2995586	chr1:224205046-224205047	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs375613223	chr1:224205075-224205076	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs2933459	chr1:224205084-224205085	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs367742099	chr1:224205108-224205109	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs202162333	chr1:224205135-224205136	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs189460045	chr1:224205156-224205157	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs192419725	chr1:224205172-224205173	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs2995585	chr1:224205187-224205188	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs2995584	chr1:224205238-224205239	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs183801373	chr1:224205258-224205259	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs527529877	chr1:224205265-224205266	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs200539125	chr1:224205291-224205292	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs61548243	chr1:224205314-224205315	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs548661223	chr1:224205318-224205319	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs377226459	chr1:224205373-224205374	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs370450520	chr1:224205398-224205399	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs531186059	chr1:224205403-224205404	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs549338658	chr1:224205499-224205500	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs571238112	chr1:224205515-224205516	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs57756374	chr1:224205520-224205521	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs372545156	chr1:224205577-224205578	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs2933460	chr1:224205654-224205655	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs2995842	chr1:224205715-224205716	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs548113546	chr1:224205760-224205761	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs200550239	chr1:224205834-224205835	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs566131112	chr1:224205837-224205838	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs10916149	chr1:224206090-224206091	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
48	rs555075399	chr1:224206102-224206103	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs189427484	chr1:224206113-224206114	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs537558050	chr1:224206133-224206134	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:97)

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
Acute lymphoblastic leukemia	21098271	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
Endometrioid adenocarcinoma	16974079	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
Congenital diaphragmatic hernia	21085971	CNVD
Mental retardation	19951919	CNVD
Non-syndromic sensorineural hearing loss	17873649	CNVD
Basal cell lymphoma	17053054	CNVD
Developmental delay	21147756	CNVD
Autism	14699429	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	20808228	CNVD
Fumarase deficiency	21572526	CNVD
Autism	17483303	CNVD
Kartagener syndrome	16639409	CNVD
Congenital abnormalities	21549014	CNVD
Developmental delay	21549014	CNVD
Mental retardation	21549014	CNVD
small cell lung cancer	20016488	CNVD
Myelofibrosis	22110671	CNVD
Liver carcinoma	19366792	CNVD
Leukoplakia	24403051	CNVD
Congenital diaphragmatic hernia	21525063	CNVD
Glioblastoma multiforme	21138945	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Cancer	20164920	CNVD
Cancer	17060936	CNVD
Schizophrenia	23813976	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:138 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:224199000-224204400	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr1:224199200-224204400	ZNF genes & repeats	Primary T cells from cord blood	blood
3	chr1:224199200-224204400	ZNF genes & repeats	Gastric	stomach
4	chr1:224204000-224207200	Weak transcription	Skeletal Muscle Female	skeletal muscle
5	chr1:224204200-224207200	Weak transcription	Adipose Nuclei	Adipose
6	chr1:224204200-224208600	Weak transcription	Liver	Liver
7	chr1:224204200-224209000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
8	chr1:224204200-224210400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
9	chr1:224204200-224210400	Weak transcription	Monocytes-CD14+_RO01746	blood
10	chr1:224204400-224207000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr1:224207200-224207400	Enhancers	Adipose Nuclei	Adipose
12	chr1:224207200-224210000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
13	chr1:224210000-224210200	Enhancers	Ovary	ovary
14	chr1:224210000-224210400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
15	chr1:224210000-224210600	Enhancers	NHDF-Ad	bronchial
16	chr1:224210400-224210600	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
17	chr1:224210600-224214400	Weak transcription	NHDF-Ad	bronchial
18	chr1:224210800-224211000	Enhancers	Ovary	ovary
19	chr1:224223400-224225400	Enhancers	K562	blood
20	chr1:224225400-224228800	Weak transcription	K562	blood
21	chr1:224227200-224227400	Enhancers	Gastric	stomach
22	chr1:224227400-224228800	Weak transcription	Gastric	stomach
23	chr1:224228800-224229200	Enhancers	Rectal Mucosa Donor 29	rectum
24	chr1:224228800-224229200	Enhancers	Sigmoid Colon	Sigmoid Colon
25	chr1:224228800-224229600	Enhancers	Gastric	stomach
26	chr1:224228800-224229800	Enhancers	K562	blood
27	chr1:224229000-224229200	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
28	chr1:224229000-224229400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
29	chr1:224229000-224229400	Enhancers	Rectal Mucosa Donor 31	rectum
30	chr1:224229400-224230800	Enhancers	HUVEC	blood vessel
31	chr1:224229600-224230600	Weak transcription	Gastric	stomach
32	chr1:224229800-224230200	Weak transcription	K562	blood
33	chr1:224230000-224230400	Enhancers	GM12878-XiMat	blood
34	chr1:224230200-224230400	Enhancers	K562	blood
35	chr1:224230400-224230600	Enhancers	Muscle Satellite Cultured Cells	--
36	chr1:224230400-224230800	Bivalent Enhancer	IMR90 fetal lung fibroblasts Cell Line	lung
37	chr1:224230400-224230800	Enhancers	Fetal Lung	lung
38	chr1:224230400-224230800	Flanking Active TSS	K562	blood
39	chr1:224230600-224230800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
40	chr1:224230600-224230800	Enhancers	Gastric	stomach
41	chr1:224230600-224230800	Enhancers	Lung	lung
42	chr1:224230600-224230800	Enhancers	NHDF-Ad	bronchial
43	chr1:224231000-224231600	Weak transcription	K562	blood
44	chr1:224231400-224232600	Enhancers	Fetal Brain Male	brain
45	chr1:224231800-224232000	Enhancers	K562	blood
46	chr1:224232400-224240400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
47	chr1:224235000-224235200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
48	chr1:224235200-224236000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
49	chr1:224235600-224236000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
50	chr1:224235600-224236000	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin

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