Variant report

Variant	esv275335
Chromosome Location	chr1:193155443-193159711
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:168)
CpG islands
(count:122)
Chromatin interactive
region (count:5)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:168 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BHLHE40	chr1:193155686-193155886	K562	blood:	n/a	n/a
2	CTCF	chr1:193159580-193159730	GM12874	blood:	n/a	n/a
3	CTCF	chr1:193159560-193159710	SAEC	small airway:	n/a	n/a
4	CTCF	chr1:193159456-193159921	MCF-7	breast:	n/a	n/a
5	CTCF	chr1:193159607-193159742	MCF-7	breast:	n/a	n/a
6	CTCF	chr1:193159640-193159790	BJ	skin:	n/a	n/a
7	CTCF	chr1:193159620-193159770	BJ	skin:	n/a	n/a
8	CTCF	chr1:193159560-193159710	HCPEpiC	choroid plexus:	n/a	n/a
9	CTCF	chr1:193159660-193159810	HFF	foreskin:	n/a	n/a
10	CTCF	chr1:193159540-193159690	GM12872	blood:	n/a	n/a
11	CTCF	chr1:193159600-193159750	HBMEC	blood vessel:	n/a	n/a
12	CTCF	chr1:193159599-193159724	HepG2	liver:	n/a	n/a
13	CTCF	chr1:193159620-193159770	Caco-2	colon:	n/a	n/a
14	CTCF	chr1:193159380-193159530	HFF-Myc	foreskin:	n/a	n/a
15	CTCF	chr1:193159580-193159730	HBMEC	blood vessel:	n/a	n/a
16	CTCF	chr1:193159680-193159830	HAc	cerebellar:	n/a	n/a
17	CTCF	chr1:193159600-193159750	HEEpiC	esophagus:	n/a	n/a
18	CTCF	chr1:193159600-193159750	HCFaa	heart:	n/a	n/a
19	CTCF	chr1:193159560-193159710	GM12864	blood:	n/a	n/a
20	CTCF	chr1:193159560-193159710	GM12865	blood:	n/a	n/a
21	CTCF	chr1:193159500-193159650	GM12868	blood:	n/a	n/a
22	CTCF	chr1:193159640-193159790	HPAF	blood vessel:	n/a	n/a
23	CTCF	chr1:193159600-193159750	AG04449	skin:	n/a	n/a
24	CTCF	chr1:193159600-193159750	HFF-Myc	foreskin:	n/a	n/a
25	CTCF	chr1:193159580-193159730	HCM	heart:	n/a	n/a
26	CTCF	chr1:193159580-193159730	HVMF	connective:	n/a	n/a
27	CTCF	chr1:193159540-193159690	WERI-Rb-1	eye:	n/a	n/a
28	CTCF	chr1:193159660-193159810	HAc	cerebellar:	n/a	n/a
29	CTCF	chr1:193159580-193159730	HPF	lung:	n/a	n/a
30	CTCF	chr1:193159580-193159730	NHEK	skin:	n/a	n/a
31	CTCF	chr1:193159560-193159710	HMEC	breast:	n/a	n/a
32	CTCF	chr1:193159573-193159774	Hela-S3	cervix:	n/a	n/a
33	CTCF	chr1:193159577-193159766	MCF-7	breast:	n/a	n/a
34	CTCF	chr1:193159580-193159730	GM12878	blood:	n/a	n/a
35	CTCF	chr1:193159600-193159750	HRE	kidney:	n/a	n/a
36	CTCF	chr1:193159540-193159690	GM06990	blood:	n/a	n/a
37	CTCF	chr1:193159560-193159710	AG09319	gingival:	n/a	n/a
38	CTCF	chr1:193159680-193159830	HFF-Myc	foreskin:	n/a	n/a
39	CTCF	chr1:193159700-193159850	RPTEC	kidney:	n/a	n/a
40	CTCF	chr1:193159680-193159830	GM12872	blood:	n/a	n/a
41	CTCF	chr1:193159600-193159750	HA-sp	spinal cord:	n/a	n/a
42	CTCF	chr1:193159600-193159750	AG09309	skin:	n/a	n/a
43	CTCF	chr1:193159620-193159770	GM12865	blood:	n/a	n/a
44	CTCF	chr1:193159540-193159690	AG09309	skin:	n/a	n/a
45	CTCF	chr1:193159600-193159750	Hela-S3	cervix:	n/a	n/a
46	CTCF	chr1:193159600-193159750	WERI-Rb-1	eye:	n/a	n/a
47	CTCF	chr1:193159620-193159770	GM12864	blood:	n/a	n/a
48	CTCF	chr1:193159560-193159753	A549	lung:	n/a	n/a
49	CTCF	chr1:193159600-193159750	MCF-7	breast:	n/a	n/a
50	CTCF	chr1:193159600-193159750	GM12873	blood:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:193155806-193155856	IMR90	lung:	fetal
2	chr1:193156434-193156484	LNCaP	prostate:	n/a
3	chr1:193155806-193155856	AG04450	lung:	fetal
4	chr1:193156434-193156484	SK-N-MC	brain:	n/a
5	chr1:193156434-193156484	HCT-116	colon:	n/a
6	chr1:193155806-193155856	HEEpiC	esophagus:	n/a
7	chr1:193155806-193155856	Jurkat	blood:	n/a
8	chr1:193156434-193156484	NHBE	bronchial:	n/a
9	chr1:193155806-193155856	SK-N-SH	brain:	n/a
10	chr1:193156434-193156484	RPTEC	kidney:	n/a
11	chr1:193156434-193156484	GM12892	blood:	n/a
12	chr1:193155806-193155856	HCPEpiC	choroid plexus:	n/a
13	chr1:193155806-193155856	BE2_C	brain:	n/a
14	chr1:193156434-193156484	SKMC	muscle:	n/a
15	chr1:193156434-193156484	Hepatocyte	liver:	n/a
16	chr1:193156434-193156484	ovcar-3	ovarian:	n/a
17	chr1:193155806-193155856	GM12892	blood:	n/a
18	chr1:193156434-193156484	HCPEpiC	choroid plexus:	n/a
19	chr1:193155806-193155856	HCT-116	colon:	n/a
20	chr1:193156434-193156484	HEEpiC	esophagus:	n/a
21	chr1:193156434-193156484	GM12891	blood:	n/a
22	chr1:193155806-193155856	NHBE	bronchial:	n/a
23	chr1:193155806-193155856	GM19239	blood:	n/a
24	chr1:193155806-193155856	CMK	blood:	n/a
25	chr1:193156434-193156484	IMR90	lung:	fetal
26	chr1:193155806-193155856	T-47D	breast:	n/a
27	chr1:193156434-193156484	PrEC	prostate:	n/a
28	chr1:193155806-193155856	HMEC	breast:	n/a
29	chr1:193156434-193156484	HEK293	kidney:	embryo
30	chr1:193156434-193156484	SK-N-SH_RA	brain:	n/a
31	chr1:193156434-193156484	GM12878	blood:	n/a
32	chr1:193156434-193156484	HRCEpiC	kidney:	n/a
33	chr1:193156434-193156484	HIPEpiC	eye:	n/a
34	chr1:193155806-193155856	HAEpiC	amniotic membrane:	n/a
35	chr1:193156434-193156484	GM06990	blood:	n/a
36	chr1:193156434-193156484	HCF	heart:	n/a
37	chr1:193155806-193155856	AG10803	skin:	n/a
38	chr1:193156434-193156484	Jurkat	blood:	n/a
39	chr1:193155806-193155856	K562	blood:	n/a
40	chr1:193155806-193155856	PrEC	prostate:	n/a
41	chr1:193156434-193156484	HUVEC	blood vessel:	n/a
42	chr1:193155806-193155856	SK-N-MC	brain:	n/a
43	chr1:193155806-193155856	NB4	blood:	n/a
44	chr1:193155806-193155856	HepG2	liver:	n/a
45	chr1:193155806-193155856	GM12878	blood:	n/a
46	chr1:193155806-193155856	GM06990	blood:	n/a
47	chr1:193156434-193156484	BJ	skin:	n/a
48	chr1:193156434-193156484	AG10803	skin:	n/a
49	chr1:193155806-193155856	HCM	heart:	n/a
50	chr1:193156434-193156484	T-47D	breast:	n/a

(count:5 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:193157136..193159095-chr1:193163776..193165606,2	K562	blood:
2	chr1:193156361..193159258-chr1:193169836..193172237,2	K562	blood:
3	chr1:193091690..193093803-chr1:193152706..193155451,2	K562	blood:
4	chr1:193156268..193159950-chr1:193162638..193166172,6	K562	blood:
5	chr1:193159041..193161726-chr1:193183249..193186234,2	K562	blood:

No data

Variant related genes	Relation type
B3GALT2	TF binding region
B3GALT2	CpG island

Extended variants
information (count: 146 )
Associated
traits (count: 91 )

Variant overlapped rSNPs/rCNVs (count:146 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs541925867	chr1:193155446-193155447	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs181462524	chr1:193155459-193155460	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs147589997	chr1:193155467-193155468	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs34851524	chr1:193155525-193155526	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs3795616	chr1:193155528-193155529	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs560631288	chr1:193155560-193155561	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs186047009	chr1:193155598-193155599	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs80041886	chr1:193155607-193155608	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs114526158	chr1:193155636-193155637	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs531724374	chr1:193155643-193155644	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs16835199	chr1:193155649-193155650	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs72722414	chr1:193155655-193155656	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs533739212	chr1:193155689-193155690	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs190812869	chr1:193155691-193155692	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs547152975	chr1:193155702-193155703	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs570673144	chr1:193155707-193155708	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs372050140	chr1:193155753-193155754	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs539694030	chr1:193155764-193155765	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs36042032	chr1:193155787-193155788	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs555916690	chr1:193155819-193155820	Weak transcription Flanking Active TSS Enhancers Active TSS	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
21	rs139329072	chr1:193155846-193155847	Weak transcription Flanking Active TSS Enhancers Active TSS	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
22	rs559774720	chr1:193155980-193155981	Weak transcription Flanking Active TSS Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs79776421	chr1:193156038-193156039	Weak transcription Flanking Active TSS Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs555500167	chr1:193156146-193156147	Weak transcription Flanking Active TSS Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs572130789	chr1:193156149-193156150	Weak transcription Flanking Active TSS Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs374008693	chr1:193156162-193156163	Weak transcription Flanking Active TSS Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs182595116	chr1:193156194-193156195	Weak transcription Flanking Active TSS Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs187302662	chr1:193156216-193156217	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs552529631	chr1:193156226-193156227	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs3079946	chr1:193156232-193156233	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs146435193	chr1:193156237-193156238	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs577493476	chr1:193156240-193156241	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs5779666	chr1:193156242-193156243	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs368123672	chr1:193156255-193156256	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs562781940	chr1:193156364-193156365	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs190892574	chr1:193156435-193156436	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
37	rs548128334	chr1:193156470-193156471	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
38	rs182654357	chr1:193156525-193156526	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs538340868	chr1:193156548-193156549	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs561858781	chr1:193156554-193156555	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs371281023	chr1:193156557-193156558	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs141589867	chr1:193156558-193156559	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs188897884	chr1:193156603-193156604	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs375762651	chr1:193156635-193156636	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs150444060	chr1:193156657-193156658	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs527294013	chr1:193156667-193156668	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs147047560	chr1:193156858-193156859	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs193085383	chr1:193156870-193156871	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs565519678	chr1:193156888-193156889	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs570605932	chr1:193156902-193156903	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:91)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Autism	22495311	CNVD
Liposarcoma	21253554	CNVD
Burkitt''s lymphoma	18698080	CNVD
Melanoma	18172304	CNVD
Rett syndrome	21593744	CNVD
Cancer	20164919	CNVD
Medulloblastoma	21979893	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
Carcinoma ex pleomorphic adenoma	18828159	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
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
Neuroblastoma	21899760	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17002787	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
Hepatocellular carcinoma	18803288	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
Lung cancer	18438408	CNVD
Metanephric adenoma	20802469	CNVD
Melanoma	20688739	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21611746	CNVD
primary effusion lymphomas	17116491	CNVD
Breast cancer	17393978	CNVD
Hepatocellular carcinoma	16750200	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Non-small cell lung cancer	19010865	CNVD
Mental retardation	17847001	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Trisomy 5 syndrome	21098271	CNVD
Glioblastoma multiforme	22286061	CNVD
Urothelial carcinoma	21177765	CNVD
Lung adenocarcinoma	17086460	CNVD
Lung cancer	17086460	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	16272173	CNVD
Mental retardation	21062444	CNVD
Liver carcinoma	19366792	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:397 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:193131800-193158600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr1:193140400-193159800	Weak transcription	Dnd41	blood
3	chr1:193140800-193161400	Weak transcription	Monocytes-CD14+_RO01746	blood
4	chr1:193144200-193160400	Weak transcription	Primary monocytes fromperipheralblood	blood
5	chr1:193148400-193161200	Weak transcription	Primary hematopoietic stem cells	blood
6	chr1:193149600-193156600	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
7	chr1:193149800-193156600	Active TSS	Brain Inferior Temporal Lobe	brain
8	chr1:193150200-193156400	Active TSS	Brain Angular Gyrus	brain
9	chr1:193150400-193157600	Active TSS	Fetal Brain Female	brain
10	chr1:193150800-193156000	Active TSS	Fetal Brain Male	brain
11	chr1:193150800-193156000	Active TSS	HSMM	muscle
12	chr1:193150800-193157000	Active TSS	HSMMtube	muscle
13	chr1:193151400-193156200	Active TSS	Brain Germinal Matrix	brain
14	chr1:193151600-193155800	Active TSS	Fetal Kidney	kidney
15	chr1:193151600-193156200	Active TSS	Fetal Muscle Leg	muscle
16	chr1:193151600-193156600	Active TSS	NHLF	lung
17	chr1:193151800-193156000	Active TSS	NHDF-Ad	bronchial
18	chr1:193152000-193156000	Active TSS	Brain Anterior Caudate	brain
19	chr1:193152000-193156200	Active TSS	Primary T helper 17 cells PMA-I stimulated	--
20	chr1:193152400-193156000	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
21	chr1:193152400-193156000	Active TSS	Fetal Intestine Large	intestine
22	chr1:193152600-193156000	Active TSS	Brain Hippocampus Middle	brain
23	chr1:193152600-193156200	Active TSS	Brain Cingulate Gyrus	brain
24	chr1:193152600-193156600	Active TSS	Fetal Stomach	stomach
25	chr1:193153400-193156000	Active TSS	Pancreatic Islets	Pancreatic Islet
26	chr1:193153600-193156000	Active TSS	Ovary	ovary
27	chr1:193153600-193156200	Active TSS	Brain Substantia Nigra	brain
28	chr1:193153600-193156400	Active TSS	Right Ventricle	heart
29	chr1:193153600-193158000	Active TSS	Right Atrium	heart
30	chr1:193154000-193155800	Enhancers	HUES48 Cell Line	embryonic stem cell
31	chr1:193154000-193155800	Active TSS	Fetal Adrenal Gland	Adrenal Gland
32	chr1:193154000-193156000	Active TSS	Duodenum Smooth Muscle	Duodenum
33	chr1:193154200-193155800	Enhancers	ES-I3 Cell Line	embryonic stem cell
34	chr1:193154200-193155800	Active TSS	Primary T regulatory cells fromperipheralblood	blood
35	chr1:193154400-193155600	Enhancers	Placenta Amnion	Placenta Amnion
36	chr1:193154400-193155800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
37	chr1:193154400-193156000	Enhancers	iPS-15b Cell Line	embryonic stem cell
38	chr1:193154600-193156000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
39	chr1:193154600-193156200	Flanking Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
40	chr1:193154600-193156200	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
41	chr1:193154600-193156200	Active TSS	Stomach Smooth Muscle	stomach
42	chr1:193154800-193155600	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
43	chr1:193154800-193155600	Enhancers	HUVEC	blood vessel
44	chr1:193154800-193155800	Enhancers	iPS-20b Cell Line	embryonic stem cell
45	chr1:193154800-193155800	Flanking Active TSS	Primary T helper memory cells from peripheral blood 1	blood
46	chr1:193154800-193155800	Active TSS	Fetal Muscle Trunk	muscle
47	chr1:193154800-193156000	Enhancers	iPS-18 Cell Line	embryonic stem cell
48	chr1:193154800-193156000	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
49	chr1:193154800-193156400	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
50	chr1:193154800-193156800	Enhancers	Primary T killer naive cells fromperipheralblood	blood

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