Variant report

Variant	esv3365605
Chromosome Location	chr1:227165479-227167477
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:16)
CpG islands
(count:61)
Chromatin interactive
region (count:10)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:16 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CTCF	chr1:227166260-227166302	GM19239	blood:	n/a	n/a
2	CTCF	chr1:227166252-227166259	GM19239	blood:	n/a	n/a
3	CTCF	chr1:227166306-227166383	GM19239	blood:	n/a	n/a
4	EGR1	chr1:227165660-227165994	K562	blood:	n/a	n/a
5	EGR1	chr1:227165754-227165959	K562	blood:	n/a	n/a
6	POLR2A	chr1:227166889-227167185	Hela-S3	cervix:	n/a	n/a
7	POLR2A	chr1:227165510-227166014	K562	blood:	n/a	n/a
8	POLR2A	chr1:227167316-227168488	HepG2	liver:	n/a	n/a
9	POLR2A	chr1:227166564-227166681	Hela-S3	cervix:	n/a	n/a
10	POLR2A	chr1:227165510-227165761	HepG2	liver:	n/a	n/a
11	POLR2A	chr1:227165366-227166192	HepG2	liver:	n/a	n/a
12	POLR2A	chr1:227164382-227167024	HL-60	blood:	n/a	n/a
13	POLR2A	chr1:227165575-227165653	Hela-S3	cervix:	n/a	n/a
14	POLR2A	chr1:227167143-227167339	K562	blood:	n/a	n/a
15	POLR2A	chr1:227166678-227167035	HepG2	liver:	n/a	n/a
16	POLR2A	chr1:227166361-227166682	HepG2	liver:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:227167020-227167070	HRE	kidney:	n/a
2	chr1:227167020-227167070	H1-hESC	embryonic stem cell:	embryo
3	chr1:227167020-227167070	NHBE	bronchial:	n/a
4	chr1:227167020-227167070	HAEpiC	amniotic membrane:	n/a
5	chr1:227167020-227167070	ProgFib	skin:	n/a
6	chr1:227167020-227167070	BE2_C	brain:	n/a
7	chr1:227167020-227167070	GM12878	blood:	n/a
8	chr1:227167020-227167070	AG10803	skin:	n/a
9	chr1:227167020-227167070	HIPEpiC	eye:	n/a
10	chr1:227167020-227167070	HMEC	breast:	n/a
11	chr1:227167020-227167070	MCF-7	breast:	n/a
12	chr1:227167020-227167070	HEK293	kidney:	embryo
13	chr1:227167020-227167070	AG09319	gingival:	n/a
14	chr1:227167020-227167070	GM06990	blood:	n/a
15	chr1:227167020-227167070	PFSK-1	brain:	n/a
16	chr1:227167020-227167070	HepG2	liver:	n/a
17	chr1:227167020-227167070	A549	lung:	n/a
18	chr1:227167020-227167070	NB4	blood:	n/a
19	chr1:227167020-227167070	HRPEpiC	eye:	n/a
20	chr1:227167020-227167070	MCF10A-Er-Src	breast:	n/a
21	chr1:227167020-227167070	PrEC	prostate:	n/a
22	chr1:227167020-227167070	GM12891	blood:	n/a
23	chr1:227167020-227167070	GM19239	blood:	n/a
24	chr1:227167020-227167070	Caco-2	colon:	n/a
25	chr1:227167020-227167070	ECC-1	luminal epithelium:	n/a
26	chr1:227167020-227167070	RPTEC	kidney:	n/a
27	chr1:227167020-227167070	CMK	blood:	n/a
28	chr1:227167020-227167070	GM12892	blood:	n/a
29	chr1:227167020-227167070	HL-60	blood:	n/a
30	chr1:227167020-227167070	HCPEpiC	choroid plexus:	n/a
31	chr1:227167020-227167070	LNCaP	prostate:	n/a
32	chr1:227167020-227167070	HEEpiC	esophagus:	n/a
33	chr1:227167020-227167070	AG04449	skin:	fetal
34	chr1:227167020-227167070	HPAEpiC	pulmonary alveolar:	n/a
35	chr1:227167020-227167070	K562	blood:	n/a
36	chr1:227167020-227167070	IMR90	lung:	fetal
37	chr1:227167020-227167070	ovcar-3	ovarian:	n/a
38	chr1:227167020-227167070	PANC-1	pancreas:	n/a
39	chr1:227167020-227167070	Hela-S3	cervix:	n/a
40	chr1:227167020-227167070	NT2-D1	testis:	n/a
41	chr1:227167020-227167070	SK-N-MC	brain:	n/a
42	chr1:227167020-227167070	SK-N-SH	brain:	n/a
43	chr1:227167020-227167070	AG09309	skin:	n/a
44	chr1:227167020-227167070	SAEC	small airway:	n/a
45	chr1:227167020-227167070	HCT-116	colon:	n/a
46	chr1:227167020-227167070	HUVEC	blood vessel:	n/a
47	chr1:227167020-227167070	AG04450	lung:	fetal
48	chr1:227167020-227167070	NHDF-neo	bronchial:	n/a
49	chr1:227167020-227167070	SKMC	muscle:	n/a
50	chr1:227167020-227167070	HCF	heart:	n/a

(count:10 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:227152242..227154390-chr1:227167200..227168802,2	MCF-7	breast:
2	chr1:227163376..227165158-chr1:227165776..227167614,2	K562	blood:
3	chr1:227165601..227167978-chr1:227173311..227176266,3	MCF-7	breast:
4	chr1:227159722..227162799-chr1:227165393..227168885,3	K562	blood:
5	chr1:227163749..227166477-chr1:227166697..227169013,2	K562	blood:
6	chr1:227167168..227168996-chr1:227169215..227170935,2	K562	blood:
7	chr1:227166708..227168288-chr1:227175078..227176909,2	MCF-7	breast:
8	chr1:227127948..227129868-chr1:227162930..227165927,2	MCF-7	breast:
9	chr1:227139663..227142101-chr1:227165412..227167064,2	K562	blood:
10	chr1:227166644..227169259-chr1:227201639..227203715,2	K562	blood:

No data

Variant related genes	Relation type
ADCK3	TF binding region
ADCK3	CpG island
ENSG00000163050	chromatin interactions

Extended variants
information (count: 152 )
Associated
traits (count: 90 )

Variant overlapped rSNPs/rCNVs (count:152 , 50 per page) page: 1 2 3 4

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1888826	chr1:227165484-227165485	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs531980636	chr1:227165490-227165491	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs116517333	chr1:227165505-227165506	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs571981520	chr1:227165576-227165577	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs532810873	chr1:227165577-227165578	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs117760107	chr1:227165599-227165600	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs114114213	chr1:227165611-227165612	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs377399620	chr1:227165612-227165613	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs75332836	chr1:227165650-227165651	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs560077747	chr1:227165679-227165680	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs528909151	chr1:227165680-227165681	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs555090955	chr1:227165719-227165720	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs149219460	chr1:227165722-227165723	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs542506546	chr1:227165731-227165732	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs145143739	chr1:227165753-227165754	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs576749242	chr1:227165759-227165760	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs540891618	chr1:227165766-227165767	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs552976725	chr1:227165792-227165793	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs574403050	chr1:227165793-227165794	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs541458699	chr1:227165800-227165801	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs113718745	chr1:227165806-227165807	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs111162992	chr1:227165816-227165817	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs544035926	chr1:227165832-227165833	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs565453633	chr1:227165850-227165851	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs532874730	chr1:227165860-227165861	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs548135320	chr1:227165866-227165867	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs559789716	chr1:227165869-227165870	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs371021243	chr1:227165879-227165880	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs548246323	chr1:227165881-227165882	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs140678488	chr1:227165890-227165891	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs530697821	chr1:227165926-227165927	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs111162994	chr1:227165929-227165930	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs193051768	chr1:227165935-227165936	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs199762444	chr1:227165937-227165938	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs370823000	chr1:227165941-227165942	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs534488059	chr1:227165969-227165970	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs553280019	chr1:227165980-227165981	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs376014691	chr1:227165995-227165996	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs574635523	chr1:227166002-227166003	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs118155348	chr1:227166042-227166043	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs550763479	chr1:227166046-227166047	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs535442735	chr1:227166060-227166061	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs556639093	chr1:227166065-227166066	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs372722465	chr1:227166081-227166082	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs575435616	chr1:227166085-227166086	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs545883027	chr1:227166097-227166098	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs200880038	chr1:227166101-227166102	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs111069272	chr1:227166102-227166103	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs541254207	chr1:227166140-227166141	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs375272574	chr1:227166146-227166147	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive 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
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
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

Chromatin state (count:200 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:227131000-227171800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
2	chr1:227147000-227177000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
3	chr1:227148600-227180800	Weak transcription	Pancreatic Islets	Pancreatic Islet
4	chr1:227154400-227165800	Weak transcription	H1 Cell Line	embryonic stem cell
5	chr1:227154400-227294200	Weak transcription	Hela-S3	cervix
6	chr1:227154800-227176800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
7	chr1:227158400-227173200	Weak transcription	K562	blood
8	chr1:227158400-227174600	Weak transcription	HUES48 Cell Line	embryonic stem cell
9	chr1:227158400-227183000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
10	chr1:227159000-227175800	Strong transcription	Primary hematopoietic stem cells short term culture	blood
11	chr1:227159800-227165800	Weak transcription	Primary hematopoietic stem cells	blood
12	chr1:227159800-227174000	Weak transcription	HUES64 Cell Line	embryonic stem cell
13	chr1:227160000-227173600	Weak transcription	A549	lung
14	chr1:227160000-227174400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
15	chr1:227160000-227174400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
16	chr1:227160000-227174800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
17	chr1:227160000-227177200	Weak transcription	GM12878-XiMat	blood
18	chr1:227160600-227165800	Enhancers	Psoas Muscle	Psoas
19	chr1:227160600-227175600	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
20	chr1:227160800-227181800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
21	chr1:227162200-227166600	Weak transcription	HUES6 Cell Line	embryonic stem cell
22	chr1:227162200-227169400	Weak transcription	Rectal Mucosa Donor 31	rectum
23	chr1:227162200-227176000	Strong transcription	Primary T cells from cord blood	blood
24	chr1:227162400-227173600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
25	chr1:227162400-227174200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
26	chr1:227162400-227174200	Weak transcription	Muscle Satellite Cultured Cells	--
27	chr1:227162400-227175200	Strong transcription	Primary monocytes fromperipheralblood	blood
28	chr1:227162400-227181600	Weak transcription	NHEK	skin
29	chr1:227162600-227174200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
30	chr1:227162600-227174200	Weak transcription	Aorta	Aorta
31	chr1:227162600-227175800	Strong transcription	Primary T helper cells fromperipheralblood	blood
32	chr1:227162600-227176600	Strong transcription	Thymus	Thymus
33	chr1:227162800-227165600	Weak transcription	H9 Cell Line	embryonic stem cell
34	chr1:227162800-227172000	Weak transcription	Placenta Amnion	Placenta Amnion
35	chr1:227162800-227173600	Weak transcription	NHLF	lung
36	chr1:227162800-227174000	Weak transcription	Osteobl	bone
37	chr1:227162800-227174200	Weak transcription	NHDF-Ad	bronchial
38	chr1:227163000-227166000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
39	chr1:227163000-227166800	Weak transcription	Esophagus	oesophagus
40	chr1:227163000-227167800	Strong transcription	Lung	lung
41	chr1:227163000-227173400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
42	chr1:227163000-227173600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
43	chr1:227163000-227174200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
44	chr1:227163000-227180000	Weak transcription	HSMM	muscle
45	chr1:227163200-227165600	Weak transcription	Duodenum Smooth Muscle	Duodenum
46	chr1:227163200-227170400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
47	chr1:227163200-227172800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
48	chr1:227163200-227174000	Weak transcription	Small Intestine	intestine
49	chr1:227163200-227175400	Strong transcription	Fetal Intestine Small	intestine
50	chr1:227163400-227165600	Weak transcription	Fetal Heart	heart

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