Variant report

Variant	nsv527874
Chromosome Location	chr1:226557878-226562779
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:38)
CpG islands
(count:61)
Chromatin interactive
region (count:9)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

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

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CUX1	chr1:226557844-226558004	GM12878	blood:	n/a	n/a
2	EBF1	chr1:226558342-226558570	GM12878	blood:	n/a	n/a
3	EBF1	chr1:226558227-226558617	GM12878	blood:	n/a	n/a
4	EBF1	chr1:226558860-226559062	GM12878	blood:	n/a	n/a
5	EBF1	chr1:226557652-226558020	GM12878	blood:	n/a	n/a
6	EBF1	chr1:226557702-226557963	GM12878	blood:	n/a	n/a
7	EBF1	chr1:226558304-226558541	GM12878	blood:	n/a	n/a
8	GATA3	chr1:226561708-226562082	T-47D	breast:	n/a	n/a
9	MAFK	chr1:226561855-226561886	HepG2	liver:	n/a	chr1:226561869-226561880 chr1:226561869-226561880
10	MAX	chr1:226558066-226558122	GM12878	blood:	n/a	n/a
11	MTA3	chr1:226558151-226558655	GM12878	blood:	n/a	n/a
12	PAX5	chr1:226558214-226558695	GM12892	blood:	n/a	chr1:226558439-226558458
13	PAX5	chr1:226558055-226558600	GM12878	blood:	n/a	chr1:226558439-226558458
14	PAX5	chr1:226558340-226558592	GM12891	blood:	n/a	chr1:226558439-226558458
15	PAX5	chr1:226558101-226558739	GM12878	blood:	n/a	chr1:226558439-226558458
16	PAX5	chr1:226558239-226558640	GM12892	blood:	n/a	chr1:226558439-226558458
17	PAX5	chr1:226558335-226558575	GM12878	blood:	n/a	chr1:226558439-226558458
18	PAX5	chr1:226558273-226558585	GM12891	blood:	n/a	chr1:226558439-226558458
19	PAX5	chr1:226558195-226558589	GM12878	blood:	n/a	chr1:226558439-226558458
20	POLR2A	chr1:226562211-226562223	H1-hESC	embryonic stem cell:	n/a	n/a
21	POLR2A	chr1:226562516-226562656	H1-hESC	embryonic stem cell:	n/a	n/a
22	POLR2A	chr1:226560888-226560951	K562	blood:	n/a	n/a
23	POLR2A	chr1:226562690-226562701	Hela-S3	cervix:	n/a	n/a
24	POLR2A	chr1:226561049-226561057	K562	blood:	n/a	n/a
25	POLR2A	chr1:226562278-226562397	H1-hESC	embryonic stem cell:	n/a	n/a
26	POLR2A	chr1:226562223-226562804	PFSK-1	brain:	n/a	n/a
27	POLR2A	chr1:226560725-226561039	K562	blood:	n/a	n/a
28	POLR2A	chr1:226560405-226560872	K562	blood:	n/a	n/a
29	POLR2A	chr1:226558043-226558094	K562	blood:	n/a	n/a
30	POLR2A	chr1:226560552-226560931	Hela-S3	cervix:	n/a	n/a
31	POLR2A	chr1:226562706-226562942	Hela-S3	cervix:	n/a	n/a
32	POLR2A	chr1:226560989-226561033	K562	blood:	n/a	n/a
33	POLR2A	chr1:226561506-226561700	HepG2	liver:	n/a	n/a
34	POLR2A	chr1:226562226-226562538	Hela-S3	cervix:	n/a	n/a
35	POLR2A	chr1:226561122-226561156	K562	blood:	n/a	n/a
36	RUNX3	chr1:226558279-226558617	GM12878	blood:	n/a	n/a
37	TBL1XR1	chr1:226558342-226558427	GM12878	blood:	n/a	n/a
38	WRNIP1	chr1:226558553-226558569	GM12878	blood:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:226558496-226558546	HepG2	liver:	n/a
2	chr1:226558496-226558546	T-47D	breast:	n/a
3	chr1:226558496-226558546	IMR90	lung:	fetal
4	chr1:226558496-226558546	GM12892	blood:	n/a
5	chr1:226558496-226558546	HPAEpiC	pulmonary alveolar:	n/a
6	chr1:226558496-226558546	SKMC	muscle:	n/a
7	chr1:226558496-226558546	NH-A	brain:	n/a
8	chr1:226558496-226558546	HEEpiC	esophagus:	n/a
9	chr1:226558496-226558546	GM19239	blood:	n/a
10	chr1:226558496-226558546	AG09319	gingival:	n/a
11	chr1:226558496-226558546	U87	brain:	n/a
12	chr1:226558496-226558546	HMEC	breast:	n/a
13	chr1:226558496-226558546	HAEpiC	amniotic membrane:	n/a
14	chr1:226558496-226558546	SK-N-SH_RA	brain:	n/a
15	chr1:226558496-226558546	Jurkat	blood:	n/a
16	chr1:226558496-226558546	NHDF-neo	bronchial:	n/a
17	chr1:226558496-226558546	HL-60	blood:	n/a
18	chr1:226558496-226558546	ProgFib	skin:	n/a
19	chr1:226558496-226558546	H1-hESC	embryonic stem cell:	embryo
20	chr1:226558496-226558546	HCPEpiC	choroid plexus:	n/a
21	chr1:226558496-226558546	HNPCEpiC	eye:	n/a
22	chr1:226558496-226558546	ECC-1	luminal epithelium:	n/a
23	chr1:226558496-226558546	HRE	kidney:	n/a
24	chr1:226558496-226558546	GM06990	blood:	n/a
25	chr1:226558496-226558546	Caco-2	colon:	n/a
26	chr1:226558496-226558546	BJ	skin:	n/a
27	chr1:226558496-226558546	Hela-S3	cervix:	n/a
28	chr1:226558496-226558546	HUVEC	blood vessel:	n/a
29	chr1:226558496-226558546	NT2-D1	testis:	n/a
30	chr1:226558496-226558546	HEK293	kidney:	embryo
31	chr1:226558496-226558546	ovcar-3	ovarian:	n/a
32	chr1:226558496-226558546	SK-N-SH	brain:	n/a
33	chr1:226558496-226558546	MCF10A-Er-Src	breast:	n/a
34	chr1:226558496-226558546	MCF-7	breast:	n/a
35	chr1:226558496-226558546	HIPEpiC	eye:	n/a
36	chr1:226558496-226558546	PANC-1	pancreas:	n/a
37	chr1:226558496-226558546	AG10803	skin:	n/a
38	chr1:226558496-226558546	SAEC	small airway:	n/a
39	chr1:226558496-226558546	CMK	blood:	n/a
40	chr1:226558496-226558546	AoSMC	blood vessel:	n/a
41	chr1:226558496-226558546	LNCaP	prostate:	n/a
42	chr1:226558496-226558546	HCM	heart:	n/a
43	chr1:226558496-226558546	A549	lung:	n/a
44	chr1:226558496-226558546	AG04449	skin:	fetal
45	chr1:226558496-226558546	NB4	blood:	n/a
46	chr1:226558496-226558546	PFSK-1	brain:	n/a
47	chr1:226558496-226558546	BE2_C	brain:	n/a
48	chr1:226558496-226558546	AG09309	skin:	n/a
49	chr1:226558496-226558546	GM12878	blood:	n/a
50	chr1:226558496-226558546	SK-N-MC	brain:	n/a

(count:9 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:226496175..226497867-chr1:226559586..226561925,2	MCF-7	breast:
2	chr1:226496099..226498370-chr1:226560413..226562179,2	MCF-7	breast:
3	chr1:226562550..226565404-chr1:226590775..226592475,2	K562	blood:
4	chr1:226560810..226567347-chr1:226567516..226572343,10	K562	blood:
5	chr1:226554977..226556502-chr1:226556594..226558224,2	MCF-7	breast:
6	chr1:226549132..226551095-chr1:226561499..226564076,2	K562	blood:
7	chr1:226543345..226545616-chr1:226561219..226563673,2	MCF-7	breast:
8	chr1:226560876..226565984-chr1:226590975..226596145,7	K562	blood:
9	chr1:226550494..226555291-chr1:226557365..226562090,4	MCF-7	breast:

No data

Variant related genes	Relation type
PARP1	TF binding region
PARP1	CpG island
ENSG00000183814	chromatin interactions
ENSG00000143799	chromatin interactions

Extended variants
information (count: 216 )
Associated
traits (count: 90 )

Variant overlapped rSNPs/rCNVs (count:216 , 50 per page) page: 1 2 3 4 5

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs3219110	chr1:226557878-226557879	Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs377257955	chr1:226557890-226557891	Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs555268913	chr1:226557894-226557895	Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs576652242	chr1:226557950-226557951	Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs539994448	chr1:226557971-226557972	Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs113876287	chr1:226557983-226557984	Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs150978127	chr1:226557998-226557999	Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs532708589	chr1:226557999-226558000	Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs2271350	chr1:226558007-226558008	Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs184159355	chr1:226558034-226558035	Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs559458353	chr1:226558042-226558043	Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs2271351	chr1:226558053-226558054	Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs544073904	chr1:226558054-226558055	Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs370344345	chr1:226558090-226558091	Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs201047974	chr1:226558101-226558102	Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs377034872	chr1:226558113-226558114	Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs370279480	chr1:226558128-226558129	Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs372662420	chr1:226558165-226558166	Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs139484215	chr1:226558197-226558198	Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs13306138	chr1:226558207-226558208	Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs377495505	chr1:226558216-226558217	Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs149789506	chr1:226558228-226558229	Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs370628368	chr1:226558238-226558239	Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs375447539	chr1:226558249-226558250	Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs199840266	chr1:226558266-226558267	Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs73089862	chr1:226558271-226558272	Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs547505335	chr1:226558287-226558288	Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs370904841	chr1:226558299-226558300	Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs566015842	chr1:226558312-226558313	Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs116578167	chr1:226558318-226558319	Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs554659447	chr1:226558341-226558342	Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs576721916	chr1:226558344-226558345	Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs537349688	chr1:226558394-226558395	Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs559255734	chr1:226558398-226558399	Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs577530596	chr1:226558453-226558454	Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs145714057	chr1:226558467-226558468	Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs559519725	chr1:226558487-226558488	Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs187463400	chr1:226558490-226558491	Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs111700994	chr1:226558496-226558497	Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs112457785	chr1:226558510-226558511	Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs530483020	chr1:226558534-226558535	Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs115213846	chr1:226558633-226558634	Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs564008681	chr1:226558747-226558748	Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs374274306	chr1:226558751-226558752	Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs528295794	chr1:226558776-226558777	Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs546371676	chr1:226558781-226558782	Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs566207596	chr1:226558859-226558860	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs368574366	chr1:226558867-226558868	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs114730401	chr1:226558929-226558930	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs548619195	chr1:226558980-226558981	Strong transcription Weak transcription Genic enhancers Enhancers	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	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:242 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:226538400-226566800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr1:226543000-226558400	Strong transcription	Primary hematopoietic stem cells	blood
3	chr1:226543000-226578400	Strong transcription	Breast Myoepithelial Primary Cells	Breast
4	chr1:226543000-226582800	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr1:226543000-226590800	Strong transcription	Primary hematopoietic stem cells short term culture	blood
6	chr1:226543000-226590800	Strong transcription	Monocytes-CD14+_RO01746	blood
7	chr1:226543000-226591400	Strong transcription	Primary T cells from cord blood	blood
8	chr1:226543200-226588600	Strong transcription	HUES6 Cell Line	embryonic stem cell
9	chr1:226543200-226588600	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
10	chr1:226543400-226580400	Strong transcription	H1 Cell Line	embryonic stem cell
11	chr1:226543400-226590200	Strong transcription	iPS-20b Cell Line	embryonic stem cell
12	chr1:226543400-226591400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr1:226543600-226590400	Strong transcription	Primary T helper cells fromperipheralblood	blood
14	chr1:226543600-226591400	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
15	chr1:226544200-226590400	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
16	chr1:226544600-226580200	Strong transcription	Stomach Smooth Muscle	stomach
17	chr1:226544600-226580400	Strong transcription	Fetal Stomach	stomach
18	chr1:226544600-226591800	Strong transcription	Dnd41	blood
19	chr1:226544800-226558000	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
20	chr1:226544800-226563400	Strong transcription	Spleen	Spleen
21	chr1:226544800-226590800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
22	chr1:226545000-226580400	Strong transcription	Sigmoid Colon	Sigmoid Colon
23	chr1:226545000-226590800	Strong transcription	Primary monocytes fromperipheralblood	blood
24	chr1:226545200-226558600	Strong transcription	Brain Angular Gyrus	brain
25	chr1:226545200-226560000	Strong transcription	Colon Smooth Muscle	Colon
26	chr1:226545200-226569800	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
27	chr1:226545200-226580200	Strong transcription	Ovary	ovary
28	chr1:226545200-226580400	Strong transcription	Fetal Intestine Large	intestine
29	chr1:226545200-226581000	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
30	chr1:226545200-226581200	Strong transcription	Adipose Nuclei	Adipose
31	chr1:226545200-226582600	Strong transcription	Rectal Mucosa Donor 29	rectum
32	chr1:226545200-226582800	Strong transcription	Duodenum Mucosa	Duodenum
33	chr1:226545400-226560600	Strong transcription	Brain Anterior Caudate	brain
34	chr1:226545400-226560800	Strong transcription	Brain Inferior Temporal Lobe	brain
35	chr1:226545400-226568000	Strong transcription	Liver	Liver
36	chr1:226545400-226580000	Strong transcription	HUES64 Cell Line	embryonic stem cell
37	chr1:226545400-226580200	Strong transcription	Thymus	Thymus
38	chr1:226545400-226580400	Strong transcription	H9 Cell Line	embryonic stem cell
39	chr1:226545400-226580400	Strong transcription	Cortex derived primary cultured neurospheres	brain
40	chr1:226545400-226580400	Strong transcription	Rectal Smooth Muscle	rectum
41	chr1:226545400-226581400	Strong transcription	Duodenum Smooth Muscle	Duodenum
42	chr1:226545400-226584000	Strong transcription	iPS-18 Cell Line	embryonic stem cell
43	chr1:226545400-226590600	Strong transcription	HUES48 Cell Line	embryonic stem cell
44	chr1:226545600-226580200	Strong transcription	Esophagus	oesophagus
45	chr1:226545600-226581400	Strong transcription	Primary T helper naive cells from peripheral blood	blood
46	chr1:226545600-226582800	Strong transcription	Fetal Thymus	thymus
47	chr1:226545600-226588200	Strong transcription	Primary T cells fromperipheralblood	blood
48	chr1:226545800-226579800	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
49	chr1:226545800-226579800	Strong transcription	Primary neutrophils fromperipheralblood	blood
50	chr1:226545800-226580200	Strong transcription	Primary T killer naive cells fromperipheralblood	blood

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