Variant report

Variant	esv1801609
Chromosome Location	chr1:226027323-226036309
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:646)
CpG islands
(count:244)
Chromatin interactive
region (count:29)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:646 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:226033582-226033809	HepG2	liver:	n/a	n/a
2	ATF2	chr1:226033441-226033940	H1-hESC	embryonic stem cell:	n/a	n/a
3	ATF2	chr1:226035614-226036271	GM12878	blood:	n/a	n/a
4	BACH1	chr1:226033629-226033650	H1-hESC	embryonic stem cell:	n/a	n/a
5	BCL3	chr1:226033373-226033982	A549	lung:	n/a	n/a
6	BCL3	chr1:226033089-226033715	A549	lung:	n/a	n/a
7	BCLAF1	chr1:226035620-226036437	GM12878	blood:	n/a	n/a
8	BHLHE40	chr1:226035781-226036130	GM12878	blood:	n/a	n/a
9	BHLHE40	chr1:226033488-226033821	K562	blood:	n/a	n/a
10	BRCA1	chr1:226033520-226033817	HepG2	liver:	n/a	n/a
11	BRCA1	chr1:226035747-226036097	GM12878	blood:	n/a	n/a
12	BRCA1	chr1:226033564-226033803	H1-hESC	embryonic stem cell:	n/a	n/a
13	CBX3	chr1:226033446-226033847	K562	blood:	n/a	n/a
14	CCNT2	chr1:226030380-226030585	K562	blood:	n/a	n/a
15	CEBPB	chr1:226033562-226033800	Hela-S3	cervix:	n/a	n/a
16	CEBPB	chr1:226033576-226033722	H1-hESC	embryonic stem cell:	n/a	n/a
17	CEBPD	chr1:226033522-226033874	HepG2	liver:	n/a	n/a
18	CHD2	chr1:226033592-226033669	K562	blood:	n/a	n/a
19	CHD2	chr1:226033345-226033855	H1-hESC	embryonic stem cell:	n/a	n/a
20	CHD2	chr1:226035700-226036005	GM12878	blood:	n/a	n/a
21	CHD2	chr1:226029882-226029884	K562	blood:	n/a	n/a
22	CHD2	chr1:226033376-226033616	HepG2	liver:	n/a	n/a
23	CHD2	chr1:226031279-226031457	K562	blood:	n/a	n/a
24	CHD2	chr1:226028611-226028642	K562	blood:	n/a	n/a
25	CHD2	chr1:226033513-226033725	Hela-S3	cervix:	n/a	n/a
26	CTCF	chr1:226033580-226033730	BJ	skin:	n/a	n/a
27	CTCF	chr1:226033411-226033895	H1-hESC	embryonic stem cell:	n/a	n/a
28	CTCF	chr1:226029898-226029900	H1-hESC	embryonic stem cell:	n/a	n/a
29	CTCF	chr1:226033580-226033730	HEK293	kidney:	n/a	n/a
30	CTCF	chr1:226033620-226033770	NHLF	lung:	n/a	n/a
31	CTCF	chr1:226033537-226033813	MCF-7	breast:	n/a	n/a
32	CTCF	chr1:226033614-226033745	GM13976	blood:	n/a	n/a
33	CTCF	chr1:226035780-226035930	GM12873	blood:	n/a	chr1:226035827-226035840
34	CTCF	chr1:226033537-226033813	Medullo	brain:	n/a	n/a
35	CTCF	chr1:226033563-226033818	ProgFib	skin:	n/a	n/a
36	CTCF	chr1:226033557-226033770	GM13977	blood:	n/a	n/a
37	CTCF	chr1:226033558-226033805	GM12878	blood:	n/a	n/a
38	CTCF	chr1:226033543-226033820	H1-hESC	embryonic stem cell:	n/a	n/a
39	CTCF	chr1:226033600-226033750	HVMF	connective:	n/a	n/a
40	CTCF	chr1:226029915-226030024	NHEK	skin:	n/a	chr1:226029972-226029985
41	CTCF	chr1:226033580-226033730	HBMEC	blood vessel:	n/a	n/a
42	CTCF	chr1:226034140-226034290	HVMF	connective:	n/a	n/a
43	CTCF	chr1:226033361-226033954	MCF-7	breast:	n/a	n/a
44	CTCF	chr1:226033897-226033992	NHEK	skin:	n/a	n/a
45	CTCF	chr1:226033580-226033730	Hela-S3	cervix:	n/a	n/a
46	CTCF	chr1:226033499-226033730	SK-N-SH_RA	brain:	n/a	n/a
47	CTCF	chr1:226033600-226033750	K562	blood:	n/a	n/a
48	CTCF	chr1:226033600-226033750	Hela-S3	cervix:	n/a	n/a
49	CTCF	chr1:226033620-226033770	BE2_C	brain:	n/a	n/a
50	CTCF	chr1:226033600-226033750	HBMEC	blood vessel:	n/a	n/a

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:226033217-226033267	NHBE	bronchial:	n/a
2	chr1:226033217-226033267	LNCaP	prostate:	n/a
3	chr1:226033550-226033600	HL-60	blood:	n/a
4	chr1:226036279-226036329	BJ	skin:	n/a
5	chr1:226033217-226033267	NT2-D1	testis:	n/a
6	chr1:226033016-226033066	GM06990	blood:	n/a
7	chr1:226033016-226033066	SK-N-SH	brain:	n/a
8	chr1:226033550-226033600	BJ	skin:	n/a
9	chr1:226033550-226033600	MCF10A-Er-Src	breast:	n/a
10	chr1:226033217-226033267	HCPEpiC	choroid plexus:	n/a
11	chr1:226033016-226033066	AG09319	gingival:	n/a
12	chr1:226033217-226033267	GM06990	blood:	n/a
13	chr1:226033550-226033600	NT2-D1	testis:	n/a
14	chr1:226033217-226033267	SKMC	muscle:	n/a
15	chr1:226033217-226033267	HEEpiC	esophagus:	n/a
16	chr1:226033550-226033600	AG09309	skin:	n/a
17	chr1:226033217-226033267	SAEC	small airway:	n/a
18	chr1:226033016-226033066	H1-hESC	embryonic stem cell:	embryo
19	chr1:226033550-226033600	IMR90	lung:	fetal
20	chr1:226033016-226033066	SAEC	small airway:	n/a
21	chr1:226033217-226033267	ECC-1	luminal epithelium:	n/a
22	chr1:226033550-226033600	SKMC	muscle:	n/a
23	chr1:226036279-226036329	MCF10A-Er-Src	breast:	n/a
24	chr1:226036279-226036329	HepG2	liver:	n/a
25	chr1:226033016-226033066	K562	blood:	n/a
26	chr1:226033217-226033267	NB4	blood:	n/a
27	chr1:226036279-226036329	HRPEpiC	eye:	n/a
28	chr1:226033217-226033267	U87	brain:	n/a
29	chr1:226033217-226033267	Jurkat	blood:	n/a
30	chr1:226033217-226033267	RPTEC	kidney:	n/a
31	chr1:226033217-226033267	BJ	skin:	n/a
32	chr1:226036279-226036329	AG04450	lung:	fetal
33	chr1:226033217-226033267	GM12891	blood:	n/a
34	chr1:226033217-226033267	A549	lung:	n/a
35	chr1:226033550-226033600	HPAEpiC	pulmonary alveolar:	n/a
36	chr1:226033016-226033066	PANC-1	pancreas:	n/a
37	chr1:226033016-226033066	HRCEpiC	kidney:	n/a
38	chr1:226033550-226033600	MCF-7	breast:	n/a
39	chr1:226033550-226033600	NH-A	brain:	n/a
40	chr1:226033016-226033066	HepG2	liver:	n/a
41	chr1:226033016-226033066	NB4	blood:	n/a
42	chr1:226033217-226033267	HRCEpiC	kidney:	n/a
43	chr1:226036279-226036329	HL-60	blood:	n/a
44	chr1:226033550-226033600	SAEC	small airway:	n/a
45	chr1:226033016-226033066	Hepatocyte	liver:	n/a
46	chr1:226033550-226033600	LNCaP	prostate:	n/a
47	chr1:226033016-226033066	GM19239	blood:	n/a
48	chr1:226033217-226033267	H1-hESC	embryonic stem cell:	embryo
49	chr1:226033550-226033600	SK-N-SH	brain:	n/a
50	chr1:226033016-226033066	A549	lung:	n/a

(count:29 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:226021203..226023917-chr1:226026955..226030143,3	K562	blood:
2	chr1:226030085..226032295-chr1:226067898..226070113,2	MCF-7	breast:
3	chr1:225662402..225663343-chr1:226032820..226034152,12	MCF-7	breast:
4	chr1:226032510..226034899-chr1:226069383..226071490,2	MCF-7	breast:
5	chr1:225821970..225824548-chr1:226027169..226028727,2	K562	blood:
6	chr1:226022223..226024431-chr1:226025111..226027659,2	MCF-7	breast:
7	chr1:226032235..226034217-chr1:226150384..226152008,2	K562	blood:
8	chr1:226025881..226027741-chr1:226105867..226108259,2	K562	blood:
9	chr1:225662312..225663277-chr1:226032721..226034082,11	MCF-7	breast:
10	chr1:226033230..226036408-chr1:226061975..226066194,3	MCF-7	breast:
11	chr1:226034669..226036597-chr1:226045740..226048084,2	K562	blood:
12	chr1:225662368..225663228-chr1:226027050..226027785,2	K562	blood:
13	chr1:225840519..225842068-chr1:226029667..226032109,2	MCF-7	breast:
14	chr1:226027447..226029935-chr1:226154706..226156516,2	K562	blood:
15	chr1:226033213..226034060-chr1:226163734..226164318,2	K562	blood:
16	chr1:225964435..225966967-chr1:226028850..226030577,3	MCF-7	breast:
17	chr1:226025653..226027789-chr1:226114675..226116510,2	K562	blood:
18	chr1:226025810..226027984-chr1:226031798..226033532,2	MCF-7	breast:
19	chr1:226032890..226033728-chr14:71284226..71284855,2	MCF-7	breast:
20	chr1:226025810..226027984-chr1:226031798..226033532,2	MCF-7	breast:
21	chr1:225964257..225969087-chr1:226030786..226035881,7	K562	blood:
22	chr1:226032252..226033753-chr1:226185534..226188258,2	K562	blood:
23	chr1:226028800..226031173-chr1:226165446..226167469,2	MCF-7	breast:
24	chr1:225963673..225968224-chr1:226032543..226034938,4	MCF-7	breast:
25	chr1:226036089..226038052-chr1:226109986..226111681,2	MCF-7	breast:
26	chr1:225998663..226000298-chr1:226028489..226031143,2	MCF-7	breast:
27	chr1:225963873..225967033-chr1:226031330..226035962,4	MCF-7	breast:
28	chr1:225965253..225967050-chr1:226028471..226030639,2	K562	blood:
29	chr1:225964834..225965851-chr1:226033204..226034086,4	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TMEM63A-1	chr1:226034181-226034223	ENSG00000242861.1
2	lnc-TMEM63A-1	chr1:226028584-226028888	ENSG00000242861.1

No data

Variant related genes	Relation type
TMEM63A	TF binding region
ENSG00000242861	TF binding region
TMEM63A	CpG island
ENSG00000242861	CpG island
ENSG00000213032	chromatin interactions
ENSG00000143751	chromatin interactions
ENSG00000143742	chromatin interactions
ENSG00000143811	chromatin interactions
ENSG00000196187	chromatin interactions
ENSG00000154380	chromatin interactions

Extended variants
information (count: 465 )
Associated
traits (count: 92 )

Variant overlapped rSNPs/rCNVs (count:465 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4149226	chr1:226027323-226027324	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs368019910	chr1:226027335-226027336	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs534356479	chr1:226027432-226027433	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs577492460	chr1:226027450-226027451	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs556030923	chr1:226027460-226027461	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs567227953	chr1:226027468-226027469	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs113362462	chr1:226027470-226027471	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs538192664	chr1:226027514-226027515	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs368919117	chr1:226027520-226027521	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs371433338	chr1:226027534-226027535	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs141680636	chr1:226027538-226027539	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs34143170	chr1:226027548-226027549	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs56132313	chr1:226027550-226027551	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs35561387	chr1:226027569-226027570	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs374886258	chr1:226027574-226027575	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs56300109	chr1:226027575-226027576	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs148730399	chr1:226027579-226027580	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs35967527	chr1:226027585-226027586	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs572022944	chr1:226027588-226027589	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs548700197	chr1:226027593-226027594	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs371279887	chr1:226027607-226027608	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs369274884	chr1:226027611-226027612	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs560773113	chr1:226027613-226027614	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs35073925	chr1:226027630-226027631	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs544656267	chr1:226027631-226027632	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs2292568	chr1:226027659-226027660	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs45449793	chr1:226027660-226027661	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs1803538	chr1:226027677-226027678	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs143164964	chr1:226027735-226027736	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs551816454	chr1:226027745-226027746	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs372688661	chr1:226027755-226027756	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs372701419	chr1:226027760-226027761	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs542368263	chr1:226027761-226027762	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs377018215	chr1:226027762-226027763	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs528020400	chr1:226027770-226027771	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs373021713	chr1:226027771-226027772	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs567889511	chr1:226027786-226027787	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs55706532	chr1:226027864-226027865	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs549799799	chr1:226027870-226027871	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs562596640	chr1:226027877-226027878	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs571275299	chr1:226027899-226027900	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs538210443	chr1:226027932-226027933	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs553383052	chr1:226027956-226027957	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs45515500	chr1:226028133-226028134	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs551177133	chr1:226028145-226028146	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs189926919	chr1:226028161-226028162	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs554579927	chr1:226028236-226028237	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs717759	chr1:226028264-226028265	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs11805420	chr1:226028289-226028290	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs180961292	chr1:226028300-226028301	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	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
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
Developmental delay	21147756	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
Lung adenocarcinoma	21935476	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:521 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:226013400-226031800	Weak transcription	Fetal Kidney	kidney
2	chr1:226013600-226052600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr1:226013800-226032000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
4	chr1:226013800-226037200	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr1:226014000-226032800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
6	chr1:226014600-226035600	Weak transcription	Small Intestine	intestine
7	chr1:226014800-226047800	Weak transcription	Psoas Muscle	Psoas
8	chr1:226015400-226032400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
9	chr1:226015400-226033200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
10	chr1:226015600-226033600	Weak transcription	K562	blood
11	chr1:226016000-226051000	Weak transcription	NH-A	brain
12	chr1:226016400-226033400	Strong transcription	Fetal Intestine Small	intestine
13	chr1:226016800-226033600	Weak transcription	Primary monocytes fromperipheralblood	blood
14	chr1:226017400-226049800	Weak transcription	HUVEC	blood vessel
15	chr1:226020400-226032000	Weak transcription	Aorta	Aorta
16	chr1:226020400-226033400	Weak transcription	Pancreatic Islets	Pancreatic Islet
17	chr1:226020600-226027600	Weak transcription	Primary T cells from cord blood	blood
18	chr1:226020600-226042000	Weak transcription	Hela-S3	cervix
19	chr1:226020600-226042400	Weak transcription	HSMM	muscle
20	chr1:226020800-226033400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
21	chr1:226020800-226033800	Weak transcription	Muscle Satellite Cultured Cells	--
22	chr1:226021000-226033400	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
23	chr1:226022200-226033200	Strong transcription	HUES6 Cell Line	embryonic stem cell
24	chr1:226022200-226033200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
25	chr1:226022400-226028000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr1:226022600-226028200	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
27	chr1:226022800-226029800	Weak transcription	Fetal Thymus	thymus
28	chr1:226022800-226030000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
29	chr1:226022800-226033800	Weak transcription	Stomach Mucosa	stomach
30	chr1:226023000-226039600	Weak transcription	NHDF-Ad	bronchial
31	chr1:226023400-226029000	Strong transcription	HUES48 Cell Line	embryonic stem cell
32	chr1:226023600-226030000	Weak transcription	Right Atrium	heart
33	chr1:226023800-226028600	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
34	chr1:226023800-226028600	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
35	chr1:226023800-226028800	Strong transcription	Brain Cingulate Gyrus	brain
36	chr1:226023800-226029800	Strong transcription	Liver	Liver
37	chr1:226023800-226035800	Weak transcription	Fetal Brain Male	brain
38	chr1:226024000-226031200	Strong transcription	Adipose Nuclei	Adipose
39	chr1:226024000-226032800	Strong transcription	Stomach Smooth Muscle	stomach
40	chr1:226024400-226029200	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
41	chr1:226024400-226030000	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
42	chr1:226024400-226033200	Strong transcription	Fetal Muscle Leg	muscle
43	chr1:226024600-226032600	Strong transcription	Fetal Stomach	stomach
44	chr1:226024600-226032800	Strong transcription	Skeletal Muscle Female	skeletal muscle
45	chr1:226024600-226034000	Weak transcription	Primary hematopoietic stem cells	blood
46	chr1:226024800-226027800	Strong transcription	Cortex derived primary cultured neurospheres	brain
47	chr1:226024800-226028600	Strong transcription	Breast Myoepithelial Primary Cells	Breast
48	chr1:226024800-226028600	Strong transcription	Rectal Mucosa Donor 31	rectum
49	chr1:226024800-226030000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
50	chr1:226025000-226028000	Strong transcription	Placenta	Placenta

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