Variant report

Variant	nsv998420
Chromosome Location	chr1:227228591-227275031
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:214)
CpG islands
(count:61)
Chromatin interactive
region (count:38)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:214 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:227232193-227232430	K562	blood:	n/a	n/a
2	ARID3A	chr1:227231537-227231737	K562	blood:	n/a	n/a
3	ARID3A	chr1:227258535-227258732	K562	blood:	n/a	n/a
4	ATF1	chr1:227258521-227258708	K562	blood:	n/a	n/a
5	ATF3	chr1:227258350-227258816	HCT-116	colon:	n/a	n/a
6	ATF3	chr1:227258443-227258716	K562	blood:	n/a	n/a
7	BACH1	chr1:227231455-227231670	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr1:227231445-227231759	K562	blood:	n/a	n/a
9	BATF	chr1:227260782-227261061	GM12878	blood:	n/a	n/a
10	BATF	chr1:227260814-227261065	GM12878	blood:	n/a	n/a
11	BCL11A	chr1:227260773-227261059	GM12878	blood:	n/a	n/a
12	CEBPB	chr1:227258415-227258759	HepG2	liver:	n/a	chr1:227258577-227258588 chr1:227258576-227258587
13	CEBPB	chr1:227246204-227246547	IMR90	lung:	n/a	n/a
14	CEBPB	chr1:227258398-227258770	K562	blood:	n/a	chr1:227258577-227258588 chr1:227258576-227258587
15	CEBPB	chr1:227231385-227231813	IMR90	lung:	n/a	n/a
16	CEBPB	chr1:227260879-227261153	IMR90	lung:	n/a	n/a
17	CEBPB	chr1:227258330-227258746	K562	blood:	n/a	chr1:227258577-227258588 chr1:227258576-227258587
18	CEBPB	chr1:227231508-227231769	K562	blood:	n/a	n/a
19	CEBPB	chr1:227258338-227258863	HCT-116	colon:	n/a	chr1:227258577-227258588 chr1:227258576-227258587
20	CEBPB	chr1:227258288-227258871	HCT-116	colon:	n/a	chr1:227258577-227258588 chr1:227258576-227258587
21	CEBPB	chr1:227258415-227258755	IMR90	lung:	n/a	chr1:227258577-227258588 chr1:227258576-227258587
22	CEBPB	chr1:227270310-227270472	K562	blood:	n/a	n/a
23	CEBPB	chr1:227230023-227230323	K562	blood:	n/a	n/a
24	CEBPB	chr1:227258420-227258694	K562	blood:	n/a	chr1:227258577-227258588 chr1:227258576-227258587
25	CEBPB	chr1:227258453-227258691	H1-hESC	embryonic stem cell:	n/a	chr1:227258577-227258588 chr1:227258576-227258587
26	CEBPB	chr1:227231524-227231767	A549	lung:	n/a	n/a
27	CEBPB	chr1:227231468-227231709	Hela-S3	cervix:	n/a	n/a
28	CEBPB	chr1:227270333-227270533	H1-hESC	embryonic stem cell:	n/a	n/a
29	CEBPB	chr1:227258445-227258752	A549	lung:	n/a	chr1:227258577-227258588 chr1:227258576-227258587
30	CEBPB	chr1:227256353-227256415	H1-hESC	embryonic stem cell:	n/a	n/a
31	CEBPB	chr1:227258422-227258767	Hela-S3	cervix:	n/a	chr1:227258577-227258588 chr1:227258576-227258587
32	CEBPB	chr1:227230055-227230283	A549	lung:	n/a	n/a
33	CTCF	chr1:227231920-227232070	HMF	breast:	n/a	n/a
34	CTCF	chr1:227231900-227232050	HCPEpiC	choroid plexus:	n/a	n/a
35	CTCF	chr1:227233562-227233603	Fibrobl	skin:	n/a	n/a
36	CTCF	chr1:227264944-227264971	GM13976	blood:	n/a	n/a
37	CTCF	chr1:227231700-227231850	HVMF	connective:	n/a	n/a
38	CTCF	chr1:227231860-227232010	HMF	breast:	n/a	n/a
39	CTCF	chr1:227231880-227232030	AoAF	blood vessel:	n/a	n/a
40	CTCF	chr1:227232000-227232150	AG04450	lung:	n/a	n/a
41	CTCF	chr1:227272440-227272730	GM12867	blood:	n/a	n/a
42	CTCF	chr1:227270309-227270369	LNCaP	prostate:	n/a	n/a
43	CTCF	chr1:227254880-227255030	HEK293	kidney:	n/a	n/a
44	CUX1	chr1:227232670-227232690	K562	blood:	n/a	n/a
45	E2F4	chr1:227235958-227236444	MCF10A-Er-Src	breast:	n/a	n/a
46	E2F4	chr1:227260837-227261161	MCF10A-Er-Src	breast:	n/a	n/a
47	E2F4	chr1:227238126-227238298	MCF10A-Er-Src	breast:	n/a	n/a
48	E2F4	chr1:227237441-227237822	MCF10A-Er-Src	breast:	n/a	n/a
49	E2F4	chr1:227267937-227268108	MCF10A-Er-Src	breast:	n/a	n/a
50	E2F4	chr1:227231329-227231726	MCF10A-Er-Src	breast:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:227260129-227260179	HAEpiC	amniotic membrane:	n/a
2	chr1:227260129-227260179	GM06990	blood:	n/a
3	chr1:227260129-227260179	SKMC	muscle:	n/a
4	chr1:227260129-227260179	MCF-7	breast:	n/a
5	chr1:227260129-227260179	BE2_C	brain:	n/a
6	chr1:227260129-227260179	NHBE	bronchial:	n/a
7	chr1:227260129-227260179	A549	lung:	n/a
8	chr1:227260129-227260179	CMK	blood:	n/a
9	chr1:227260129-227260179	HMEC	breast:	n/a
10	chr1:227260129-227260179	MCF10A-Er-Src	breast:	n/a
11	chr1:227260129-227260179	ECC-1	luminal epithelium:	n/a
12	chr1:227260129-227260179	ovcar-3	ovarian:	n/a
13	chr1:227260129-227260179	SK-N-SH	brain:	n/a
14	chr1:227260129-227260179	NHDF-neo	bronchial:	n/a
15	chr1:227260129-227260179	HepG2	liver:	n/a
16	chr1:227260129-227260179	Hela-S3	cervix:	n/a
17	chr1:227260129-227260179	HRE	kidney:	n/a
18	chr1:227260129-227260179	HRCEpiC	kidney:	n/a
19	chr1:227260129-227260179	AG10803	skin:	n/a
20	chr1:227260129-227260179	PFSK-1	brain:	n/a
21	chr1:227260129-227260179	IMR90	lung:	fetal
22	chr1:227260129-227260179	NH-A	brain:	n/a
23	chr1:227260129-227260179	GM12878	blood:	n/a
24	chr1:227260129-227260179	PrEC	prostate:	n/a
25	chr1:227260129-227260179	HCPEpiC	choroid plexus:	n/a
26	chr1:227260129-227260179	HIPEpiC	eye:	n/a
27	chr1:227260129-227260179	RPTEC	kidney:	n/a
28	chr1:227260129-227260179	U87	brain:	n/a
29	chr1:227260129-227260179	HEEpiC	esophagus:	n/a
30	chr1:227260129-227260179	GM19239	blood:	n/a
31	chr1:227260129-227260179	LNCaP	prostate:	n/a
32	chr1:227260129-227260179	HL-60	blood:	n/a
33	chr1:227260129-227260179	GM12892	blood:	n/a
34	chr1:227260129-227260179	SAEC	small airway:	n/a
35	chr1:227260129-227260179	HCM	heart:	n/a
36	chr1:227260129-227260179	GM12891	blood:	n/a
37	chr1:227260129-227260179	HEK293	kidney:	embryo
38	chr1:227260129-227260179	AoSMC	blood vessel:	n/a
39	chr1:227260129-227260179	BJ	skin:	n/a
40	chr1:227260129-227260179	NT2-D1	testis:	n/a
41	chr1:227260129-227260179	HCT-116	colon:	n/a
42	chr1:227260129-227260179	HPAEpiC	pulmonary alveolar:	n/a
43	chr1:227260129-227260179	SK-N-MC	brain:	n/a
44	chr1:227260129-227260179	ProgFib	skin:	n/a
45	chr1:227260129-227260179	K562	blood:	n/a
46	chr1:227260129-227260179	HNPCEpiC	eye:	n/a
47	chr1:227260129-227260179	PANC-1	pancreas:	n/a
48	chr1:227260129-227260179	AG09319	gingival:	n/a
49	chr1:227260129-227260179	Jurkat	blood:	n/a
50	chr1:227260129-227260179	AG09309	skin:	n/a

(count:38 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:227243831..227246541-chr1:227247776..227250757,2	K562	blood:
2	chr1:227258899..227260884-chr1:227261569..227263920,2	K562	blood:
3	chr1:227231949..227233855-chr1:227255369..227258277,2	K562	blood:
4	chr1:227219115..227221995-chr1:227227439..227229511,2	K562	blood:
5	chr1:227267691..227268598-chr5:174748538..174749384,2	MCF-7	breast:
6	chr1:227224836..227227359-chr1:227231406..227233044,2	K562	blood:
7	chr1:227242900..227245161-chr1:227250146..227252441,3	K562	blood:
8	chr1:227256237..227258373-chr1:227281662..227284397,2	K562	blood:
9	chr1:227263840..227266585-chr1:227275633..227278048,3	K562	blood:
10	chr1:227243831..227246541-chr1:227247776..227250757,2	K562	blood:
11	chr1:227230140..227234774-chr1:227236431..227241922,5	K562	blood:
12	chr1:227249781..227252416-chr1:227257576..227259161,2	K562	blood:
13	chr1:227248469..227250587-chr1:227251655..227253321,2	K562	blood:
14	chr1:227247700..227249846-chr1:227255373..227257295,2	K562	blood:
15	chr1:227231345..227233578-chr1:227235477..227237603,2	MCF-7	breast:
16	chr1:227259571..227263475-chr1:227264453..227268699,4	K562	blood:
17	chr1:227259571..227263475-chr1:227264453..227268699,4	K562	blood:
18	chr1:227230140..227234774-chr1:227236431..227241922,5	K562	blood:
19	chr1:227259676..227262107-chr1:227264453..227267335,2	K562	blood:
20	chr1:227236504..227239220-chr1:227240349..227243242,4	K562	blood:
21	chr1:227246764..227248668-chr1:227249328..227251525,2	MCF-7	breast:
22	chr1:227236504..227239220-chr1:227240349..227243242,4	K562	blood:
23	chr1:227100437..227100984-chr1:227264267..227265039,2	K562	blood:
24	chr1:227231345..227233578-chr1:227235477..227237603,2	MCF-7	breast:
25	chr1:227236590..227238961-chr1:227241573..227243242,3	K562	blood:
26	chr1:227225377..227226974-chr1:227228914..227231037,2	K562	blood:
27	chr1:227246764..227248668-chr1:227249328..227251525,2	MCF-7	breast:
28	chr1:227249781..227252416-chr1:227257576..227259161,2	K562	blood:
29	chr1:227248469..227250587-chr1:227251655..227253321,2	K562	blood:
30	chr1:227231949..227233855-chr1:227255369..227258277,2	K562	blood:
31	chr1:227250275..227252416-chr1:227256127..227259076,3	K562	blood:
32	chr1:227250275..227252416-chr1:227256127..227259076,3	K562	blood:
33	chr1:227236590..227238961-chr1:227241573..227243242,3	K562	blood:
34	chr1:227274632..227277428-chr1:227279390..227281436,2	K562	blood:
35	chr1:227127569..227129155-chr1:227257063..227258978,2	MCF-7	breast:
36	chr1:227270688..227272597-chr1:227288564..227290914,2	MCF-7	breast:
37	chr1:227247700..227249846-chr1:227255373..227257295,2	K562	blood:
38	chr1:227242900..227245161-chr1:227250146..227252441,3	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ADCK3-5	chr1:227237319-227238751	NONHSAT009913

No data

Variant related genes	Relation type
CDC42BPA	TF binding region
CDC42BPA	CpG island
ENSG00000163050	chromatin interactions
ENSG00000143776	chromatin interactions

Extended variants
information (count: 1717 )
Associated
traits (count: 92 )

Variant overlapped rSNPs/rCNVs (count:1717 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11802395	chr1:227228591-227228592	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs541659564	chr1:227228626-227228627	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs112836792	chr1:227228633-227228634	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs530752067	chr1:227228637-227228638	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs546061247	chr1:227228643-227228644	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs564012759	chr1:227228661-227228662	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs528093850	chr1:227228744-227228745	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs564501056	chr1:227228768-227228769	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs75173200	chr1:227228779-227228780	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs78984226	chr1:227228780-227228781	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs75397616	chr1:227228781-227228782	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs113206853	chr1:227228841-227228842	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs187209094	chr1:227228845-227228846	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs61216705	chr1:227228850-227228851	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs60483746	chr1:227228913-227228914	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs148780294	chr1:227228943-227228944	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs1029063	chr1:227228946-227228947	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
18	rs11803919	chr1:227228955-227228956	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
19	rs191683928	chr1:227228997-227228998	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs540193067	chr1:227229021-227229022	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs559224055	chr1:227229039-227229040	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs571124530	chr1:227229040-227229041	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs535025289	chr1:227229083-227229084	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs553353375	chr1:227229102-227229103	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs575030486	chr1:227229138-227229139	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs542298042	chr1:227229188-227229189	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs564875223	chr1:227229201-227229202	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs532442548	chr1:227229274-227229275	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs556908918	chr1:227229283-227229284	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs183519910	chr1:227229297-227229298	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs545647370	chr1:227229306-227229307	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs200553447	chr1:227229315-227229316	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs74140241	chr1:227229341-227229342	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs539888337	chr1:227229360-227229361	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs554084472	chr1:227229376-227229377	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs561338849	chr1:227229389-227229390	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs187115326	chr1:227229443-227229444	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs550639267	chr1:227229461-227229462	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs190419041	chr1:227229488-227229489	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs182290446	chr1:227229581-227229582	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs568947838	chr1:227229632-227229633	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs568830636	chr1:227229634-227229635	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs531150186	chr1:227229648-227229649	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs571955967	chr1:227229719-227229720	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs552762630	chr1:227229785-227229786	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs144804139	chr1:227229794-227229795	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs147601765	chr1:227229820-227229821	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs140391882	chr1:227229828-227229829	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs186622519	chr1:227229842-227229843	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs73089746	chr1:227229875-227229876	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	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
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
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:623 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:227154400-227294200	Weak transcription	Hela-S3	cervix
2	chr1:227177400-227255200	Weak transcription	Small Intestine	intestine
3	chr1:227178400-227271200	Weak transcription	Psoas Muscle	Psoas
4	chr1:227183200-227240400	Weak transcription	Colonic Mucosa	Colon
5	chr1:227184000-227234000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr1:227190600-227272600	Weak transcription	Lung	lung
7	chr1:227203000-227278800	Weak transcription	Pancreas	Pancrea
8	chr1:227207600-227242000	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
9	chr1:227209000-227231000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
10	chr1:227209000-227234600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
11	chr1:227209000-227272400	Weak transcription	Fetal Intestine Small	intestine
12	chr1:227209200-227301600	Weak transcription	Placenta Amnion	Placenta Amnion
13	chr1:227210600-227245800	Weak transcription	NHEK	skin
14	chr1:227214800-227329200	Weak transcription	Right Ventricle	heart
15	chr1:227215600-227230400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
16	chr1:227216800-227231400	Weak transcription	A549	lung
17	chr1:227216800-227235000	Weak transcription	Skeletal Muscle Male	skeletal muscle
18	chr1:227216800-227239400	Weak transcription	Brain Cingulate Gyrus	brain
19	chr1:227216800-227287600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
20	chr1:227217000-227234000	Weak transcription	Fetal Brain Male	brain
21	chr1:227217000-227264400	Weak transcription	NHLF	lung
22	chr1:227217000-227271400	Weak transcription	Sigmoid Colon	Sigmoid Colon
23	chr1:227217000-227278800	Weak transcription	Placenta	Placenta
24	chr1:227217200-227241800	Weak transcription	HepG2	liver
25	chr1:227219600-227234800	Weak transcription	NH-A	brain
26	chr1:227220600-227231000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
27	chr1:227220600-227236800	Weak transcription	H9 Cell Line	embryonic stem cell
28	chr1:227220600-227255800	Weak transcription	Gastric	stomach
29	chr1:227220600-227272600	Weak transcription	Aorta	Aorta
30	chr1:227220600-227288000	Weak transcription	Colon Smooth Muscle	Colon
31	chr1:227220800-227256800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
32	chr1:227222000-227229400	Weak transcription	K562	blood
33	chr1:227222000-227253000	Weak transcription	Rectal Smooth Muscle	rectum
34	chr1:227222600-227256800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
35	chr1:227223000-227236600	Weak transcription	Brain Anterior Caudate	brain
36	chr1:227223400-227245800	Weak transcription	Osteobl	bone
37	chr1:227224600-227229600	Strong transcription	HSMM	muscle
38	chr1:227226200-227228600	Strong transcription	Duodenum Smooth Muscle	Duodenum
39	chr1:227226600-227235200	Weak transcription	Brain Substantia Nigra	brain
40	chr1:227226600-227270800	Weak transcription	Fetal Brain Female	brain
41	chr1:227226800-227229200	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
42	chr1:227226800-227233000	Weak transcription	Duodenum Mucosa	Duodenum
43	chr1:227226800-227233400	Weak transcription	Fetal Stomach	stomach
44	chr1:227226800-227233600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
45	chr1:227226800-227237800	Weak transcription	Brain Hippocampus Middle	brain
46	chr1:227226800-227238000	Weak transcription	Primary hematopoietic stem cells	blood
47	chr1:227226800-227260400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
48	chr1:227226800-227272400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
49	chr1:227226800-227278400	Weak transcription	Brain Inferior Temporal Lobe	brain
50	chr1:227226800-227285600	Weak transcription	Brain Germinal Matrix	brain

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