Variant report

Variant	esv1831035
Chromosome Location	chr1:228758016-228782866
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1162)
CpG islands
(count:183)
Chromatin interactive
region (count:2)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1162 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr1:228782482-228782665	H1-hESC	embryonic stem cell:	n/a	n/a
2	BCL3	chr1:228771159-228771418	GM12878	blood:	n/a	n/a
3	BCL3	chr1:228757836-228758031	GM12878	blood:	n/a	n/a
4	BCL3	chr1:228782396-228784122	A549	lung:	n/a	chr1:228784016-228784025 chr1:228783302-228783315 chr1:228783943-228783956 chr1:228783147-228783156 chr1:228782764-228782773
5	BCL3	chr1:228782408-228783961	A549	lung:	n/a	chr1:228783302-228783315 chr1:228783943-228783956 chr1:228783147-228783156 chr1:228782764-228782773
6	BHLHE40	chr1:228771339-228771364	GM12878	blood:	n/a	n/a
7	BHLHE40	chr1:228782373-228782758	GM12878	blood:	n/a	n/a
8	BHLHE40	chr1:228771166-228771539	K562	blood:	n/a	n/a
9	BHLHE40	chr1:228782486-228782780	HepG2	liver:	n/a	n/a
10	BHLHE40	chr1:228782393-228782773	K562	blood:	n/a	n/a
11	BRCA1	chr1:228782522-228782954	Hela-S3	cervix:	n/a	n/a
12	BRCA1	chr1:228771344-228771359	GM12878	blood:	n/a	n/a
13	CBX3	chr1:228765596-228766337	K562	blood:	n/a	n/a
14	CBX3	chr1:228768957-228769762	K562	blood:	n/a	n/a
15	CBX3	chr1:228767896-228768693	K562	blood:	n/a	n/a
16	CBX3	chr1:228760952-228762196	K562	blood:	n/a	n/a
17	CBX3	chr1:228756779-228759666	K562	blood:	n/a	n/a
18	CBX3	chr1:228780121-228782451	K562	blood:	n/a	n/a
19	CBX3	chr1:228780079-228780837	K562	blood:	n/a	n/a
20	CBX3	chr1:228759936-228766629	K562	blood:	n/a	n/a
21	CBX3	chr1:228776817-228778581	K562	blood:	n/a	n/a
22	CBX3	chr1:228756716-228760610	K562	blood:	n/a	n/a
23	CBX3	chr1:228773494-228774641	K562	blood:	n/a	n/a
24	CBX3	chr1:228763642-228764366	K562	blood:	n/a	n/a
25	CBX3	chr1:228766654-228767753	K562	blood:	n/a	n/a
26	CBX3	chr1:228779133-228779900	K562	blood:	n/a	n/a
27	CBX3	chr1:228774646-228775517	K562	blood:	n/a	n/a
28	CBX3	chr1:228767906-228768647	K562	blood:	n/a	n/a
29	CBX3	chr1:228773469-228774313	K562	blood:	n/a	n/a
30	CBX3	chr1:228762327-228762990	K562	blood:	n/a	n/a
31	CBX3	chr1:228772523-228773375	K562	blood:	n/a	n/a
32	CBX3	chr1:228781248-228782265	K562	blood:	n/a	n/a
33	CBX3	chr1:228779767-228780083	K562	blood:	n/a	n/a
34	CBX3	chr1:228774747-228775535	K562	blood:	n/a	n/a
35	CBX3	chr1:228770156-228772097	K562	blood:	n/a	n/a
36	CBX3	chr1:228768708-228770057	K562	blood:	n/a	n/a
37	CBX3	chr1:228764417-228765547	K562	blood:	n/a	n/a
38	CBX3	chr1:228771125-228772105	K562	blood:	n/a	n/a
39	CBX3	chr1:228766705-228767765	K562	blood:	n/a	n/a
40	CBX3	chr1:228772113-228773276	K562	blood:	n/a	n/a
41	CBX3	chr1:228775560-228776734	K562	blood:	n/a	n/a
42	CBX3	chr1:228770193-228771056	K562	blood:	n/a	n/a
43	CBX3	chr1:228775571-228779732	K562	blood:	n/a	n/a
44	CCNT2	chr1:228782549-228782559	K562	blood:	n/a	n/a
45	CCNT2	chr1:228771161-228771539	K562	blood:	n/a	n/a
46	CEBPB	chr1:228759206-228759599	K562	blood:	n/a	n/a
47	CEBPB	chr1:228760026-228760632	GM12878	blood:	n/a	n/a
48	CEBPB	chr1:228770360-228770948	GM12878	blood:	n/a	n/a
49	CEBPB	chr1:228775652-228776334	GM12878	blood:	n/a	n/a
50	CEBPB	chr1:228781615-228782032	K562	blood:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:228773464-228773514	U87	brain:	n/a
2	chr1:228773464-228773514	Hepatocyte	liver:	n/a
3	chr1:228773464-228773514	Jurkat	blood:	n/a
4	chr1:228773514-228773564	HL-60	blood:	n/a
5	chr1:228773514-228773564	ECC-1	luminal epithelium:	n/a
6	chr1:228773514-228773564	PANC-1	pancreas:	n/a
7	chr1:228773464-228773514	AG04449	skin:	fetal
8	chr1:228773464-228773514	HCF	heart:	n/a
9	chr1:228773464-228773514	HEK293	kidney:	embryo
10	chr1:228773514-228773564	PFSK-1	brain:	n/a
11	chr1:228773464-228773514	HMEC	breast:	n/a
12	chr1:228782809-228782859	SK-N-MC	brain:	n/a
13	chr1:228773514-228773564	HepG2	liver:	n/a
14	chr1:228773514-228773564	NHDF-neo	bronchial:	n/a
15	chr1:228782809-228782859	U87	brain:	n/a
16	chr1:228782809-228782859	T-47D	breast:	n/a
17	chr1:228773464-228773514	Caco-2	colon:	n/a
18	chr1:228782809-228782859	Jurkat	blood:	n/a
19	chr1:228773464-228773514	AG09309	skin:	n/a
20	chr1:228773514-228773564	SK-N-SH	brain:	n/a
21	chr1:228782809-228782859	K562	blood:	n/a
22	chr1:228773514-228773564	HAEpiC	amniotic membrane:	n/a
23	chr1:228782809-228782859	SKMC	muscle:	n/a
24	chr1:228782809-228782859	ovcar-3	ovarian:	n/a
25	chr1:228773464-228773514	HRE	kidney:	n/a
26	chr1:228782809-228782859	HRCEpiC	kidney:	n/a
27	chr1:228773464-228773514	GM06990	blood:	n/a
28	chr1:228782809-228782859	MCF10A-Er-Src	breast:	n/a
29	chr1:228773514-228773564	HCPEpiC	choroid plexus:	n/a
30	chr1:228773464-228773514	AoSMC	blood vessel:	n/a
31	chr1:228773464-228773514	MCF10A-Er-Src	breast:	n/a
32	chr1:228773514-228773564	MCF-7	breast:	n/a
33	chr1:228782809-228782859	AG04450	lung:	fetal
34	chr1:228782809-228782859	AoSMC	blood vessel:	n/a
35	chr1:228773464-228773514	RPTEC	kidney:	n/a
36	chr1:228782809-228782859	Caco-2	colon:	n/a
37	chr1:228773464-228773514	Hela-S3	cervix:	n/a
38	chr1:228773464-228773514	K562	blood:	n/a
39	chr1:228773514-228773564	Caco-2	colon:	n/a
40	chr1:228773464-228773514	CMK	blood:	n/a
41	chr1:228782809-228782859	PrEC	prostate:	n/a
42	chr1:228782809-228782859	AG09319	gingival:	n/a
43	chr1:228773514-228773564	GM19239	blood:	n/a
44	chr1:228773464-228773514	NT2-D1	testis:	n/a
45	chr1:228773514-228773564	Hepatocyte	liver:	n/a
46	chr1:228773514-228773564	HEEpiC	esophagus:	n/a
47	chr1:228773464-228773514	T-47D	breast:	n/a
48	chr1:228773514-228773564	AG10803	skin:	n/a
49	chr1:228773464-228773514	ovcar-3	ovarian:	n/a
50	chr1:228782809-228782859	HCPEpiC	choroid plexus:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr1:17231506..17232339-chr1:228782832..228783652,2	Hela-S3	cervix:
2	chr1:228782241..228785119-chr1:228785249..228788137,2	K562	blood:

No data

Variant related genes	Relation type
RNA5S17	TF binding region
RNA5S10	TF binding region
RNA5S6	TF binding region
DUSP5P1	TF binding region
RNA5S12	TF binding region
RNA5S14	TF binding region
RNA5S16	TF binding region
RNA5S7	TF binding region
RNA5S13	TF binding region
RNA5S5	TF binding region
RNA5S15	TF binding region
RNA5S8	TF binding region
RNA5S9	TF binding region
RNA5S11	TF binding region
RNA5S17	CpG island
RNA5S10	CpG island
RNA5S6	CpG island
DUSP5P1	CpG island
RNA5S12	CpG island
RNA5S14	CpG island
RNA5S16	CpG island
RNA5S7	CpG island
RNA5S13	CpG island
RNA5S5	CpG island
RNA5S15	CpG island
RNA5S8	CpG island
RNA5S9	CpG island
RNA5S11	CpG island
ENSG00000183929	chromatin interactions

Extended variants
information (count: 290 )
Associated
traits (count: 90 )

Variant overlapped rSNPs/rCNVs (count:290 , 50 per page) page: 1 2 3 4 5 6

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs61825677	chr1:228758016-228758017	Bivalent/Poised TSS Flanking Active TSS Active TSS Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
2	rs61825678	chr1:228758027-228758028	Bivalent/Poised TSS Flanking Active TSS Active TSS Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
3	rs190428826	chr1:228758044-228758045	Bivalent/Poised TSS Flanking Active TSS Active TSS Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
4	rs11484728	chr1:228758055-228758056	Bivalent/Poised TSS Flanking Active TSS Active TSS Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
5	rs11484729	chr1:228758060-228758061	Bivalent/Poised TSS Flanking Active TSS Active TSS Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
6	rs11484730	chr1:228758124-228758125	Bivalent/Poised TSS Flanking Active TSS Active TSS Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
7	rs11487481	chr1:228758138-228758139	Bivalent/Poised TSS Flanking Active TSS Active TSS Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
8	rs11484731	chr1:228758140-228758141	Bivalent/Poised TSS Flanking Active TSS Active TSS Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
9	rs374779647	chr1:228758164-228758165	Bivalent/Poised TSS Flanking Active TSS Active TSS Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
10	rs1925725	chr1:228758170-228758171	Bivalent/Poised TSS Flanking Active TSS Active TSS Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
11	rs11484732	chr1:228758186-228758187	Bivalent/Poised TSS Flanking Active TSS Active TSS Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
12	rs558568148	chr1:228758188-228758189	Bivalent/Poised TSS Flanking Active TSS Active TSS Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
13	rs565793485	chr1:228758198-228758199	Bivalent/Poised TSS Flanking Active TSS Active TSS Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
14	rs534690233	chr1:228758338-228758339	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
15	rs112693194	chr1:228758473-228758474	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
16	rs113904250	chr1:228761270-228761271	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
17	rs554471947	chr1:228762072-228762073	Weak transcription	TF binding region	3 gene(s)	Overlapped CNVs	n/a
18	rs369017563	chr1:228762186-228762187	Weak transcription	TF binding region	3 gene(s)	Overlapped CNVs	n/a
19	rs543243684	chr1:228762228-228762229	Weak transcription	TF binding region	3 gene(s)	Overlapped CNVs	n/a
20	rs557270581	chr1:228762374-228762375	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
21	rs371749725	chr1:228762387-228762388	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
22	rs563216374	chr1:228762397-228762398	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
23	rs201514969	chr1:228762398-228762399	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
24	rs552780625	chr1:228762399-228762400	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
25	rs545828157	chr1:228762402-228762403	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
26	rs369969261	chr1:228762404-228762405	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
27	rs559293514	chr1:228762411-228762412	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
28	rs528566711	chr1:228762412-228762413	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
29	rs542267385	chr1:228762413-228762414	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
30	rs76054467	chr1:228762415-228762416	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
31	rs531179492	chr1:228762416-228762417	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
32	rs138968350	chr1:228762421-228762422	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
33	rs144304688	chr1:228762423-228762424	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
34	rs533630404	chr1:228762431-228762432	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
35	rs552226034	chr1:228762433-228762434	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
36	rs375379588	chr1:228762438-228762439	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
37	rs565636381	chr1:228762463-228762464	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
38	rs534430440	chr1:228762476-228762477	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
39	rs554691686	chr1:228762498-228762499	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
40	rs369435777	chr1:228762503-228762504	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
41	rs568060782	chr1:228762509-228762510	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
42	rs537280678	chr1:228762614-228762615	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
43	rs113733990	chr1:228762630-228762631	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
44	rs373312997	chr1:228762646-228762647	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
45	rs576742739	chr1:228762707-228762708	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
46	rs373146317	chr1:228762732-228762733	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
47	rs552959458	chr1:228762741-228762742	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
48	rs377620511	chr1:228762756-228762757	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
49	rs370009262	chr1:228762768-228762769	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
50	rs562236867	chr1:228762812-228762813	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:90)

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
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
Mental retardation	19951919	CNVD
Non-syndromic sensorineural hearing loss	17873649	CNVD
Basal cell lymphoma	17053054	CNVD
Autism	14699429	CNVD
Chronic lymphocytic leukemia	21546498	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
Glioblastoma multiforme	21138945	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Cancer	20164920	CNVD
Cancer	17060936	CNVD
Myelofibrosis	22110671	CNVD
abnormal development	18461090	CNVD
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Melanoma	17363583	CNVD

Chromatin state (count:456 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:228757000-228771000	Weak transcription	Right Atrium	heart
2	chr1:228757800-228758200	Bivalent/Poised TSS	H1 Cell Line	embryonic stem cell
3	chr1:228757800-228758200	Active TSS	Adipose Nuclei	Adipose
4	chr1:228757800-228758200	Active TSS	Fetal Stomach	stomach
5	chr1:228757800-228758200	Active TSS	Dnd41	blood
6	chr1:228757800-228758200	Active TSS	HSMM	muscle
7	chr1:228758000-228758200	Flanking Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
8	chr1:228764400-228764600	Weak transcription	H1 Cell Line	embryonic stem cell
9	chr1:228768600-228768800	Active TSS	Fetal Brain Female	brain
10	chr1:228768600-228769000	Bivalent/Poised TSS	H1 Cell Line	embryonic stem cell
11	chr1:228768600-228769000	Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
12	chr1:228768600-228769000	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr1:228768600-228769000	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
14	chr1:228768600-228769000	Active TSS	Primary T helper naive cells fromperipheralblood	blood
15	chr1:228768600-228769000	Active TSS	Cortex derived primary cultured neurospheres	brain
16	chr1:228768600-228769000	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
17	chr1:228768600-228769000	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
18	chr1:228768600-228769000	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
19	chr1:228768600-228769000	Bivalent/Poised TSS	Fetal Stomach	stomach
20	chr1:228768800-228769000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
21	chr1:228768800-228769000	Bivalent/Poised TSS	Fetal Brain Female	brain
22	chr1:228769000-228771000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
23	chr1:228769000-228771000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
24	chr1:228769000-228771000	Weak transcription	Cortex derived primary cultured neurospheres	brain
25	chr1:228769000-228771000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
26	chr1:228769000-228771200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
27	chr1:228770600-228770800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
28	chr1:228770800-228771000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
29	chr1:228770800-228771000	Enhancers	Primary B cells from peripheral blood	blood
30	chr1:228770800-228771000	Enhancers	Ovary	ovary
31	chr1:228770800-228771000	Enhancers	Placenta Amnion	Placenta Amnion
32	chr1:228771000-228771200	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
33	chr1:228771000-228771200	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
34	chr1:228771000-228771200	Active TSS	Primary neutrophils fromperipheralblood	blood
35	chr1:228771000-228771200	Enhancers	Primary B cells from cord blood	blood
36	chr1:228771000-228771200	Flanking Active TSS	Primary T cells fromperipheralblood	blood
37	chr1:228771000-228771200	Active TSS	Primary hematopoietic stem cells	blood
38	chr1:228771000-228771200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
39	chr1:228771000-228771200	Active TSS	Primary T helper naive cells fromperipheralblood	blood
40	chr1:228771000-228771200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
41	chr1:228771000-228771200	Active TSS	Primary T helper cells PMA-I stimulated	--
42	chr1:228771000-228771200	Active TSS	Primary T helper 17 cells PMA-I stimulated	--
43	chr1:228771000-228771200	Active TSS	Primary T helper cells fromperipheralblood	blood
44	chr1:228771000-228771200	Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
45	chr1:228771000-228771200	Bivalent Enhancer	Primary Natural Killer cells fromperipheralblood	blood
46	chr1:228771000-228771200	Active TSS	Primary T killer naive cells fromperipheralblood	blood
47	chr1:228771000-228771200	Active TSS	Cortex derived primary cultured neurospheres	brain
48	chr1:228771000-228771200	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
49	chr1:228771000-228771200	Active TSS	Adipose Nuclei	Adipose
50	chr1:228771000-228771200	Active TSS	Brain Germinal Matrix	brain

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