Variant report

Variant	esv1803377
Chromosome Location	chr1:224052449-224108920
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:889)
CpG islands
(count:61)
Chromatin interactive
region (count:20)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:889 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:224060633-224061180	K562	blood:	n/a	n/a
2	ARID3A	chr1:224074186-224074661	HepG2	liver:	n/a	n/a
3	ARID3A	chr1:224071990-224072005	K562	blood:	n/a	n/a
4	ATF1	chr1:224065655-224065775	K562	blood:	n/a	n/a
5	ATF1	chr1:224058318-224058581	K562	blood:	n/a	n/a
6	ATF1	chr1:224060830-224061199	K562	blood:	n/a	n/a
7	BATF	chr1:224100112-224100738	GM12878	blood:	n/a	chr1:224100431-224100442
8	BATF	chr1:224103998-224104234	GM12878	blood:	n/a	n/a
9	BATF	chr1:224100132-224100691	GM12878	blood:	n/a	chr1:224100431-224100442
10	BATF	chr1:224108598-224108877	GM12878	blood:	n/a	chr1:224108835-224108844
11	BATF	chr1:224095793-224096047	GM12878	blood:	n/a	n/a
12	BATF	chr1:224108555-224108855	GM12878	blood:	n/a	chr1:224108835-224108844
13	BATF	chr1:224104058-224104261	GM12878	blood:	n/a	n/a
14	BATF	chr1:224074339-224074659	GM12878	blood:	n/a	chr1:224074521-224074532 chr1:224074522-224074532
15	BATF	chr1:224074385-224074609	GM12878	blood:	n/a	chr1:224074521-224074532 chr1:224074522-224074532
16	BATF	chr1:224092998-224093284	GM12878	blood:	n/a	n/a
17	BCL11A	chr1:224103937-224104270	GM12878	blood:	n/a	chr1:224104160-224104168
18	BCL11A	chr1:224095804-224096023	GM12878	blood:	n/a	n/a
19	BCL11A	chr1:224090921-224091109	GM12878	blood:	n/a	chr1:224091090-224091098
20	BCL11A	chr1:224108051-224108199	GM12878	blood:	n/a	n/a
21	BCL11A	chr1:224093639-224093850	GM12878	blood:	n/a	n/a
22	BCL11A	chr1:224091435-224091635	GM12878	blood:	n/a	chr1:224091454-224091463
23	BCL11A	chr1:224094248-224094435	GM12878	blood:	n/a	n/a
24	BCL11A	chr1:224100059-224100720	GM12878	blood:	n/a	chr1:224100434-224100443
25	BCL11A	chr1:224095758-224096028	GM12878	blood:	n/a	n/a
26	BCL11A	chr1:224100121-224100579	GM12878	blood:	n/a	chr1:224100434-224100443
27	BCL11A	chr1:224083605-224083817	GM12878	blood:	n/a	n/a
28	BCL3	chr1:224075622-224076301	A549	lung:	n/a	chr1:224076057-224076066 chr1:224076058-224076067
29	BCL3	chr1:224075630-224076397	A549	lung:	n/a	chr1:224076057-224076066 chr1:224076058-224076067
30	BHLHE40	chr1:224108563-224108836	HepG2	liver:	n/a	n/a
31	BHLHE40	chr1:224074217-224074622	HepG2	liver:	n/a	n/a
32	BRCA1	chr1:224075566-224076253	Hela-S3	cervix:	n/a	chr1:224075656-224075663
33	CBX3	chr1:224058172-224059252	K562	blood:	n/a	n/a
34	CBX3	chr1:224060624-224061253	K562	blood:	n/a	n/a
35	CBX3	chr1:224059380-224059843	K562	blood:	n/a	n/a
36	CCNT2	chr1:224058409-224058609	K562	blood:	n/a	n/a
37	CCNT2	chr1:224060849-224061051	K562	blood:	n/a	n/a
38	CEBPB	chr1:224076187-224076381	HepG2	liver:	n/a	n/a
39	CEBPB	chr1:224074277-224074645	HepG2	liver:	n/a	chr1:224074354-224074371
40	CEBPB	chr1:224070631-224070714	A549	lung:	n/a	n/a
41	CEBPB	chr1:224075524-224076471	Hela-S3	cervix:	n/a	n/a
42	CEBPB	chr1:224058951-224059102	K562	blood:	n/a	chr1:224059023-224059034
43	CEBPB	chr1:224075262-224076440	IMR90	lung:	n/a	n/a
44	CEBPB	chr1:224058918-224059142	HepG2	liver:	n/a	chr1:224059023-224059034
45	CEBPB	chr1:224075731-224076533	A549	lung:	n/a	n/a
46	CEBPB	chr1:224075851-224076473	A549	lung:	n/a	n/a
47	CEBPD	chr1:224058241-224058840	K562	blood:	n/a	n/a
48	CEBPD	chr1:224058237-224058827	K562	blood:	n/a	n/a
49	CEBPD	chr1:224060765-224061293	K562	blood:	n/a	n/a
50	CEBPD	chr1:224060022-224060350	K562	blood:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:224075899-224075949	HPAEpiC	pulmonary alveolar:	n/a
2	chr1:224075899-224075949	PFSK-1	brain:	n/a
3	chr1:224075899-224075949	SK-N-SH_RA	brain:	n/a
4	chr1:224075899-224075949	NH-A	brain:	n/a
5	chr1:224075899-224075949	AG10803	skin:	n/a
6	chr1:224075899-224075949	HCF	heart:	n/a
7	chr1:224075899-224075949	BJ	skin:	n/a
8	chr1:224075899-224075949	HNPCEpiC	eye:	n/a
9	chr1:224075899-224075949	K562	blood:	n/a
10	chr1:224075899-224075949	AG04450	lung:	fetal
11	chr1:224075899-224075949	ECC-1	luminal epithelium:	n/a
12	chr1:224075899-224075949	HRE	kidney:	n/a
13	chr1:224075899-224075949	AG09319	gingival:	n/a
14	chr1:224075899-224075949	HRPEpiC	eye:	n/a
15	chr1:224075899-224075949	AoSMC	blood vessel:	n/a
16	chr1:224075899-224075949	HepG2	liver:	n/a
17	chr1:224075899-224075949	NHDF-neo	bronchial:	n/a
18	chr1:224075899-224075949	HRCEpiC	kidney:	n/a
19	chr1:224075899-224075949	NHBE	bronchial:	n/a
20	chr1:224075899-224075949	AG09309	skin:	n/a
21	chr1:224075899-224075949	HAEpiC	amniotic membrane:	n/a
22	chr1:224075899-224075949	T-47D	breast:	n/a
23	chr1:224075899-224075949	H1-hESC	embryonic stem cell:	embryo
24	chr1:224075899-224075949	LNCaP	prostate:	n/a
25	chr1:224075899-224075949	ProgFib	skin:	n/a
26	chr1:224075899-224075949	GM12892	blood:	n/a
27	chr1:224075899-224075949	Jurkat	blood:	n/a
28	chr1:224075899-224075949	HCM	heart:	n/a
29	chr1:224075899-224075949	SK-N-MC	brain:	n/a
30	chr1:224075899-224075949	A549	lung:	n/a
31	chr1:224075899-224075949	GM06990	blood:	n/a
32	chr1:224075899-224075949	GM19239	blood:	n/a
33	chr1:224075899-224075949	RPTEC	kidney:	n/a
34	chr1:224075899-224075949	SKMC	muscle:	n/a
35	chr1:224075899-224075949	SK-N-SH	brain:	n/a
36	chr1:224075899-224075949	NT2-D1	testis:	n/a
37	chr1:224075899-224075949	HUVEC	blood vessel:	n/a
38	chr1:224075899-224075949	Hepatocyte	liver:	n/a
39	chr1:224075899-224075949	U87	brain:	n/a
40	chr1:224075899-224075949	HCPEpiC	choroid plexus:	n/a
41	chr1:224075899-224075949	NB4	blood:	n/a
42	chr1:224075899-224075949	HCT-116	colon:	n/a
43	chr1:224075899-224075949	ovcar-3	ovarian:	n/a
44	chr1:224075899-224075949	SAEC	small airway:	n/a
45	chr1:224075899-224075949	AG04449	skin:	fetal
46	chr1:224075899-224075949	HL-60	blood:	n/a
47	chr1:224075899-224075949	MCF-7	breast:	n/a
48	chr1:224075899-224075949	PrEC	prostate:	n/a
49	chr1:224075899-224075949	MCF10A-Er-Src	breast:	n/a
50	chr1:224075899-224075949	CMK	blood:	n/a

(count:20 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:224064706..224067481-chr1:224068167..224069755,2	MCF-7	breast:
2	chr1:224031941..224034592-chr1:224054767..224056750,2	K562	blood:
3	chr1:224032805..224035351-chr1:224065902..224068634,2	MCF-7	breast:
4	chr1:224070627..224072910-chr1:224076240..224077802,2	K562	blood:
5	chr1:224033263..224035344-chr1:224063361..224065777,2	MCF-7	breast:
6	chr1:224061505..224063787-chr1:224074137..224075680,2	K562	blood:
7	chr1:223900030..223900536-chr1:224108678..224109196,2	K562	blood:
8	chr1:224039824..224041644-chr1:224060638..224062824,2	K562	blood:
9	chr1:224048345..224051041-chr1:224057644..224060087,2	K562	blood:
10	chr1:224063820..224066455-chr1:224070379..224072043,2	K562	blood:
11	chr1:224064706..224067481-chr1:224068167..224069755,2	MCF-7	breast:
12	chr1:224032494..224036254-chr1:224057433..224064259,8	K562	blood:
13	chr1:224070627..224072910-chr1:224076240..224077802,2	K562	blood:
14	chr1:224000543..224002650-chr1:224066368..224067980,2	MCF-7	breast:
15	chr1:224051052..224053013-chr1:224064265..224066927,2	K562	blood:
16	chr1:224063820..224066455-chr1:224070379..224072043,2	K562	blood:
17	chr1:224064879..224067819-chr1:224073518..224075866,3	K562	blood:
18	chr1:224064879..224067819-chr1:224073518..224075866,3	K562	blood:
19	chr1:224033607..224035143-chr1:224060636..224062476,2	MCF-7	breast:
20	chr1:224061505..224063787-chr1:224074137..224075680,2	K562	blood:

(count:2 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PARP1-4	chr1:224096672-224097019	expRegAs_chr1_21127_-
2	lnc-PARP1-3	chr1:224098433-224099085	expRegAs_chr1_21128_-

No data

Variant related genes	Relation type
ACTBP11	TF binding region
ACTBP11	CpG island
ENSG00000143514	chromatin interactions
ENSG00000162909	chromatin interactions
ENSG00000188460	chromatin interactions

Extended variants
information (count: 1559 )
Associated
traits (count: 98 )

Variant overlapped rSNPs/rCNVs (count:1559 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs138395443	chr1:224052453-224052454	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
2	rs184946241	chr1:224052460-224052461	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
3	rs545991365	chr1:224052466-224052467	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
4	rs369951072	chr1:224052476-224052477	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
5	rs373370182	chr1:224052482-224052483	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
6	rs142989232	chr1:224052510-224052511	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
7	rs190239998	chr1:224052512-224052513	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
8	rs561676362	chr1:224052523-224052524	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
9	rs546397207	chr1:224052526-224052527	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
10	rs550312435	chr1:224052529-224052530	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
11	rs563148840	chr1:224052530-224052531	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
12	rs114305322	chr1:224052536-224052537	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
13	rs60681980	chr1:224052537-224052538	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs566710701	chr1:224052538-224052539	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
15	rs534155176	chr1:224052541-224052542	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
16	rs549454300	chr1:224052551-224052552	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
17	rs182895638	chr1:224052552-224052553	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
18	rs188841532	chr1:224052565-224052566	ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs556286984	chr1:224052659-224052660	Weak transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs528664788	chr1:224052661-224052662	Weak transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs146202441	chr1:224052686-224052687	Weak transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs58266329	chr1:224052703-224052704	Weak transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs139223338	chr1:224052739-224052740	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
24	rs558111338	chr1:224052746-224052747	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
25	rs376348094	chr1:224052751-224052752	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
26	rs200099641	chr1:224052752-224052753	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
27	rs111985134	chr1:224052779-224052780	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
28	rs540091860	chr1:224052851-224052852	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs561779511	chr1:224052890-224052891	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs573656540	chr1:224052899-224052900	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs192881907	chr1:224052920-224052921	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs183490723	chr1:224052922-224052923	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs532800315	chr1:224052949-224052950	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs114645810	chr1:224052954-224052955	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs560496633	chr1:224052961-224052962	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs527870113	chr1:224052994-224052995	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs549322718	chr1:224052995-224052996	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs567706504	chr1:224053020-224053021	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs12022071	chr1:224053034-224053035	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs563585044	chr1:224053046-224053047	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs531726287	chr1:224053123-224053124	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs550281206	chr1:224053131-224053132	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs537030468	chr1:224053137-224053138	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs187900221	chr1:224053138-224053139	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs539081140	chr1:224053140-224053141	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs192419155	chr1:224053212-224053213	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs566779138	chr1:224053221-224053222	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs533940103	chr1:224053259-224053260	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs552745074	chr1:224053267-224053268	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs555292315	chr1:224053302-224053303	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:98)

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
Acute myeloid leukemia	17268525	CNVD
Lung cancer	16740712	CNVD
Renal cell carcinoma	18765545	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
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Cancer	17060936	CNVD

Chromatin state (count:236 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:224052000-224052600	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr1:224052400-224052800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr1:224052600-224057800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr1:224052800-224058200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr1:224057600-224058200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr1:224057800-224058600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
7	chr1:224057800-224059400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
8	chr1:224057800-224059400	Enhancers	iPS-15b Cell Line	embryonic stem cell
9	chr1:224057800-224060600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
10	chr1:224057800-224062000	Enhancers	K562	blood
11	chr1:224058000-224058600	Enhancers	Primary monocytes fromperipheralblood	blood
12	chr1:224058000-224059400	Enhancers	HUES6 Cell Line	embryonic stem cell
13	chr1:224058000-224059400	Enhancers	Placenta	Placenta
14	chr1:224058200-224058400	Enhancers	ES-I3 Cell Line	embryonic stem cell
15	chr1:224058200-224058600	Enhancers	H9 Cell Line	embryonic stem cell
16	chr1:224058200-224058600	Bivalent Enhancer	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr1:224058200-224058600	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
18	chr1:224058200-224058600	Bivalent Enhancer	Fetal Muscle Leg	muscle
19	chr1:224058200-224058600	Enhancers	Monocytes-CD14+_RO01746	blood
20	chr1:224058200-224058800	Bivalent Enhancer	Primary Natural Killer cells fromperipheralblood	blood
21	chr1:224058200-224059200	Enhancers	iPS-18 Cell Line	embryonic stem cell
22	chr1:224058200-224059200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
23	chr1:224058200-224059200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
24	chr1:224058400-224058600	Enhancers	Pancreas	Pancrea
25	chr1:224058400-224058800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr1:224058400-224058800	Enhancers	Dnd41	blood
27	chr1:224058400-224059000	Enhancers	H1 Cell Line	embryonic stem cell
28	chr1:224058400-224059000	Enhancers	HUES64 Cell Line	embryonic stem cell
29	chr1:224058400-224059000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
30	chr1:224058400-224059200	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
31	chr1:224058400-224059200	Enhancers	Primary neutrophils fromperipheralblood	blood
32	chr1:224058400-224059200	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
33	chr1:224058400-224059400	Bivalent/Poised TSS	HepG2	liver
34	chr1:224058600-224058800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
35	chr1:224058600-224058800	Enhancers	Placenta Amnion	Placenta Amnion
36	chr1:224058600-224059000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
37	chr1:224058600-224059000	Flanking Active TSS	Primary monocytes fromperipheralblood	blood
38	chr1:224058600-224059000	Enhancers	Primary B cells from cord blood	blood
39	chr1:224058600-224059000	Active TSS	Pancreas	Pancrea
40	chr1:224058600-224059200	Bivalent Enhancer	Fetal Muscle Trunk	muscle
41	chr1:224058600-224059400	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
42	chr1:224058800-224059200	Enhancers	HUES48 Cell Line	embryonic stem cell
43	chr1:224058800-224059200	Enhancers	Primary hematopoietic stem cells short term culture	blood
44	chr1:224058800-224059200	Active TSS	Dnd41	blood
45	chr1:224059000-224059200	Bivalent Enhancer	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
46	chr1:224059000-224059200	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
47	chr1:224059000-224059200	Enhancers	Pancreas	Pancrea
48	chr1:224059000-224059400	Enhancers	Primary monocytes fromperipheralblood	blood
49	chr1:224059000-224060000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
50	chr1:224059000-224060200	Weak transcription	HUES64 Cell Line	embryonic stem cell

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