Variant report

Variant	nsv945351
Chromosome Location	chr1:228480078-228483074
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:58)
CpG islands
(count:0)
Chromatin interactive
region (count:4)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:58 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CBX3	chr1:228481107-228481494	K562	blood:	n/a	n/a
2	CTCF	chr1:228479980-228480130	HFF-Myc	foreskin:	n/a	n/a
3	CTCF	chr1:228481700-228481850	NHDF-neo	bronchial:	n/a	n/a
4	CTCF	chr1:228479860-228480178	K562	blood:	n/a	n/a
5	CTCF	chr1:228479940-228480090	HPAF	blood vessel:	n/a	n/a
6	CTCF	chr1:228479960-228480110	HCPEpiC	choroid plexus:	n/a	n/a
7	CTCF	chr1:228479940-228480090	BJ	skin:	n/a	n/a
8	CTCF	chr1:228480420-228480570	K562	blood:	n/a	chr1:228480505-228480526
9	CTCF	chr1:228480381-228480622	K562	blood:	n/a	chr1:228480505-228480526
10	CTCF	chr1:228479981-228480085	HepG2	liver:	n/a	n/a
11	CTCF	chr1:228480474-228480539	HUVEC	blood vessel:	n/a	chr1:228480505-228480526
12	CTCF	chr1:228480460-228480581	K562	blood:	n/a	chr1:228480505-228480526
13	CTCF	chr1:228480495-228480561	GM12891	blood:	n/a	chr1:228480505-228480526
14	CTCF	chr1:228479960-228480110	HFF	foreskin:	n/a	n/a
15	CTCF	chr1:228479875-228480275	K562	blood:	n/a	n/a
16	CTCF	chr1:228480000-228480150	NHDF-neo	bronchial:	n/a	n/a
17	CTCF	chr1:228479932-228480112	K562	blood:	n/a	n/a
18	CTCF	chr1:228480476-228480546	NHEK	skin:	n/a	chr1:228480505-228480526
19	E2F6	chr1:228481111-228481497	K562	blood:	n/a	n/a
20	MAFK	chr1:228481364-228481427	K562	blood:	n/a	n/a
21	MAX	chr1:228481174-228481464	K562	blood:	n/a	chr1:228481360-228481367
22	MAX	chr1:228480322-228480719	K562	blood:	n/a	n/a
23	MAX	chr1:228481309-228481315	HepG2	liver:	n/a	n/a
24	MAX	chr1:228480497-228480610	K562	blood:	n/a	n/a
25	MAX	chr1:228481030-228481828	K562	blood:	n/a	chr1:228481360-228481367
26	MAZ	chr1:228480523-228480528	K562	blood:	n/a	n/a
27	MYC	chr1:228481278-228481384	K562	blood:	n/a	chr1:228481360-228481367
28	MYC	chr1:228482078-228482083	GM12878	blood:	n/a	n/a
29	MYC	chr1:228480384-228480669	K562	blood:	n/a	n/a
30	MYC	chr1:228481953-228482053	GM12878	blood:	n/a	n/a
31	MYC	chr1:228482172-228482269	H1-hESC	embryonic stem cell:	n/a	n/a
32	MYC	chr1:228482088-228482162	H1-hESC	embryonic stem cell:	n/a	n/a
33	MYC	chr1:228481302-228481543	K562	blood:	n/a	chr1:228481360-228481367
34	MYC	chr1:228480415-228480605	K562	blood:	n/a	n/a
35	MYC	chr1:228481317-228481399	H1-hESC	embryonic stem cell:	n/a	chr1:228481360-228481367
36	POLR2A	chr1:228481719-228481730	H1-hESC	embryonic stem cell:	n/a	n/a
37	POLR2A	chr1:228481061-228481253	HCT-116	colon:	n/a	n/a
38	POLR2A	chr1:228481205-228481308	H1-hESC	embryonic stem cell:	n/a	n/a
39	POLR2A	chr1:228481079-228481250	H1-hESC	embryonic stem cell:	n/a	n/a
40	POLR2A	chr1:228482299-228484211	K562	blood:	n/a	n/a
41	POLR2A	chr1:228479539-228480259	SK-N-MC	brain:	n/a	n/a
42	POLR2A	chr1:228482849-228482912	H1-hESC	embryonic stem cell:	n/a	n/a
43	POLR2A	chr1:228481959-228482014	Hela-S3	cervix:	n/a	n/a
44	POLR2A	chr1:228481893-228482146	H1-hESC	embryonic stem cell:	n/a	n/a
45	POLR2A	chr1:228481736-228481785	H1-hESC	embryonic stem cell:	n/a	n/a
46	POLR2A	chr1:228482033-228482348	H1-hESC	embryonic stem cell:	n/a	n/a
47	POLR2A	chr1:228481284-228481376	MCF-7	breast:	n/a	n/a
48	POLR2A	chr1:228481355-228481370	H1-hESC	embryonic stem cell:	n/a	n/a
49	POLR2A	chr1:228481890-228482018	H1-hESC	embryonic stem cell:	n/a	n/a
50	POLR2A	chr1:228482576-228482735	H1-hESC	embryonic stem cell:	n/a	n/a

No data

(count:4 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:228466929..228469506-chr1:228481575..228484301,2	MCF-7	breast:
2	chr1:228399573..228401373-chr1:228480199..228482605,2	K562	blood:
3	chr1:228479719..228482312-chr1:228644744..228646634,2	K562	blood:
4	chr1:228476724..228479773-chr1:228482640..228484624,3	K562	blood:

No data

Variant related genes	Relation type
OBSCN	TF binding region
ENSG00000154358	chromatin interactions
ENSG00000162913	chromatin interactions
ENSG00000196890	chromatin interactions
ENSG00000181218	chromatin interactions

Extended variants
information (count: 166 )
Associated
traits (count: 92 )

Variant overlapped rSNPs/rCNVs (count:166 , 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	rs140894624	chr1:228480154-228480155	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs181191144	chr1:228480167-228480168	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs576770968	chr1:228480172-228480173	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs539104629	chr1:228480180-228480181	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs149452994	chr1:228480266-228480267	Weak transcription Strong transcription Bivalent Enhancer Genic enhancers Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
6	rs1150908	chr1:228480282-228480283	Weak transcription Strong transcription Bivalent Enhancer Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs572880533	chr1:228480283-228480284	Weak transcription Strong transcription Bivalent Enhancer Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs62621834	chr1:228480317-228480318	Weak transcription Strong transcription Bivalent Enhancer Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs78661188	chr1:228480319-228480320	Weak transcription Strong transcription Bivalent Enhancer Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs575520313	chr1:228480348-228480349	Weak transcription Strong transcription Bivalent Enhancer Genic enhancers Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
11	rs370940881	chr1:228480350-228480351	Weak transcription Strong transcription Bivalent Enhancer Genic enhancers Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
12	rs544470862	chr1:228480381-228480382	Weak transcription Strong transcription Bivalent Enhancer Genic enhancers Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
13	rs375862966	chr1:228480407-228480408	ZNF genes & repeats Weak transcription Strong transcription Bivalent Enhancer Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
14	rs113015177	chr1:228480441-228480442	ZNF genes & repeats Weak transcription Strong transcription Bivalent Enhancer Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
15	rs370499630	chr1:228480444-228480445	ZNF genes & repeats Weak transcription Strong transcription Bivalent Enhancer Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
16	rs374049885	chr1:228480445-228480446	ZNF genes & repeats Weak transcription Strong transcription Bivalent Enhancer Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
17	rs367635611	chr1:228480447-228480448	ZNF genes & repeats Weak transcription Strong transcription Bivalent Enhancer Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
18	rs371511335	chr1:228480468-228480469	ZNF genes & repeats Weak transcription Strong transcription Bivalent Enhancer Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
19	rs375496047	chr1:228480480-228480481	ZNF genes & repeats Weak transcription Strong transcription Bivalent Enhancer Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
20	rs375471694	chr1:228480481-228480482	ZNF genes & repeats Weak transcription Strong transcription Bivalent Enhancer Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
21	rs113386774	chr1:228480488-228480489	ZNF genes & repeats Weak transcription Strong transcription Bivalent Enhancer Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
22	rs372247054	chr1:228480517-228480518	ZNF genes & repeats Weak transcription Strong transcription Bivalent Enhancer Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
23	rs371732928	chr1:228480522-228480523	ZNF genes & repeats Weak transcription Strong transcription Bivalent Enhancer Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
24	rs76144578	chr1:228480549-228480550	ZNF genes & repeats Weak transcription Strong transcription Bivalent Enhancer Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
25	rs3795793	chr1:228480578-228480579	ZNF genes & repeats Weak transcription Strong transcription Bivalent Enhancer Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
26	rs529315964	chr1:228480595-228480596	ZNF genes & repeats Weak transcription Strong transcription Bivalent Enhancer Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
27	rs549079165	chr1:228480637-228480638	ZNF genes & repeats Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
28	rs569065239	chr1:228480703-228480704	ZNF genes & repeats Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
29	rs186133804	chr1:228480732-228480733	ZNF genes & repeats Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
30	rs532297007	chr1:228480747-228480748	ZNF genes & repeats Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
31	rs552395704	chr1:228480788-228480789	ZNF genes & repeats Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
32	rs571883293	chr1:228480791-228480792	ZNF genes & repeats Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
33	rs565716985	chr1:228480809-228480810	ZNF genes & repeats Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
34	rs113805891	chr1:228480829-228480830	ZNF genes & repeats Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
35	rs143229935	chr1:228480856-228480857	ZNF genes & repeats Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
36	rs552665969	chr1:228480885-228480886	ZNF genes & repeats Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
37	rs566479405	chr1:228480890-228480891	ZNF genes & repeats Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
38	rs535503522	chr1:228480933-228480934	ZNF genes & repeats Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
39	rs555504393	chr1:228480958-228480959	ZNF genes & repeats Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
40	rs10158357	chr1:228480964-228480965	ZNF genes & repeats Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
41	rs78410276	chr1:228481004-228481005	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs368390592	chr1:228481005-228481006	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs371535022	chr1:228481026-228481027	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs558016567	chr1:228481053-228481054	ZNF genes & repeats Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
45	rs116357930	chr1:228481067-228481068	ZNF genes & repeats Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
46	rs540539075	chr1:228481080-228481081	ZNF genes & repeats Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
47	rs369094782	chr1:228481116-228481117	ZNF genes & repeats Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
48	rs372696460	chr1:228481122-228481123	ZNF genes & repeats Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
49	rs376717072	chr1:228481123-228481124	ZNF genes & repeats Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
50	rs140221070	chr1:228481133-228481134	ZNF genes & repeats Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:92)

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
Breast cancer	22522925	CNVD
Lung adenocarcinoma	21935476	CNVD
Melanoma	17363583	CNVD

Chromatin state (count:142 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:228455400-228484800	Weak transcription	A549	lung
2	chr1:228456400-228485800	Weak transcription	Hela-S3	cervix
3	chr1:228463800-228481400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr1:228464200-228491600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
5	chr1:228464400-228481400	Weak transcription	Duodenum Smooth Muscle	Duodenum
6	chr1:228464400-228482000	Weak transcription	Fetal Kidney	kidney
7	chr1:228464400-228489200	Strong transcription	Left Ventricle	heart
8	chr1:228464600-228481400	Weak transcription	Primary hematopoietic stem cells	blood
9	chr1:228464600-228483200	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
10	chr1:228464600-228483200	Strong transcription	Fetal Intestine Small	intestine
11	chr1:228464600-228487000	Strong transcription	Breast Myoepithelial Primary Cells	Breast
12	chr1:228465000-228483600	Strong transcription	Right Ventricle	heart
13	chr1:228465000-228498000	Weak transcription	Fetal Brain Male	brain
14	chr1:228465200-228483400	Weak transcription	Colonic Mucosa	Colon
15	chr1:228465200-228483400	Strong transcription	Fetal Stomach	stomach
16	chr1:228465600-228483400	Strong transcription	Fetal Brain Female	brain
17	chr1:228467200-228484200	Weak transcription	Sigmoid Colon	Sigmoid Colon
18	chr1:228468400-228482600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
19	chr1:228471200-228484200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
20	chr1:228471600-228481400	Weak transcription	Aorta	Aorta
21	chr1:228471800-228483400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
22	chr1:228471800-228489200	Weak transcription	Duodenum Mucosa	Duodenum
23	chr1:228472000-228482000	Strong transcription	Skeletal Muscle Female	skeletal muscle
24	chr1:228472200-228481600	Weak transcription	HUES64 Cell Line	embryonic stem cell
25	chr1:228472200-228484800	Strong transcription	Fetal Muscle Leg	muscle
26	chr1:228472200-228490000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
27	chr1:228472400-228481200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
28	chr1:228472400-228486000	Weak transcription	H9 Cell Line	embryonic stem cell
29	chr1:228472400-228486200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
30	chr1:228472600-228481400	Weak transcription	Fetal Thymus	thymus
31	chr1:228473000-228488400	Weak transcription	Pancreatic Islets	Pancreatic Islet
32	chr1:228473600-228480800	Weak transcription	Fetal Heart	heart
33	chr1:228473600-228482200	Weak transcription	Primary T helper cells fromperipheralblood	blood
34	chr1:228474200-228482800	Weak transcription	Psoas Muscle	Psoas
35	chr1:228475200-228481200	Weak transcription	Stomach Smooth Muscle	stomach
36	chr1:228475400-228481400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
37	chr1:228475400-228482200	Weak transcription	Primary T helper cells PMA-I stimulated	--
38	chr1:228475800-228481000	Weak transcription	Fetal Intestine Large	intestine
39	chr1:228476000-228480800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
40	chr1:228476000-228482600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
41	chr1:228476200-228484200	Weak transcription	Esophagus	oesophagus
42	chr1:228476600-228480600	Weak transcription	Brain Anterior Caudate	brain
43	chr1:228476600-228481200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
44	chr1:228476600-228481200	Strong transcription	Skeletal Muscle Male	skeletal muscle
45	chr1:228476800-228480400	Weak transcription	Fetal Lung	lung
46	chr1:228476800-228480400	Weak transcription	HSMMtube	muscle
47	chr1:228476800-228481000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
48	chr1:228476800-228481200	Weak transcription	HUES6 Cell Line	embryonic stem cell
49	chr1:228476800-228481200	Weak transcription	Gastric	stomach
50	chr1:228476800-228485600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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