Variant report

Variant	esv2445525
Chromosome Location	chr1:197167182-197168584
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:20)
CpG islands
(count:61)
Chromatin interactive
region (count:10)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:20 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BHLHE40	chr1:197166826-197167245	K562	blood:	n/a	n/a
2	CEBPB	chr1:197167506-197167804	K562	blood:	n/a	chr1:197167650-197167661 chr1:197167648-197167661 chr1:197167648-197167659
3	CEBPB	chr1:197167527-197167774	HepG2	liver:	n/a	chr1:197167650-197167661 chr1:197167648-197167661 chr1:197167648-197167659
4	CEBPB	chr1:197167550-197167748	A549	lung:	n/a	chr1:197167650-197167661 chr1:197167648-197167661 chr1:197167648-197167659
5	CHD2	chr1:197166995-197167184	GM12878	blood:	n/a	n/a
6	EP300	chr1:197167035-197167186	GM12878	blood:	n/a	n/a
7	FOS	chr1:197168070-197168410	MCF10A-Er-Src	breast:	n/a	n/a
8	FOS	chr1:197167830-197168438	MCF10A-Er-Src	breast:	n/a	n/a
9	FOS	chr1:197168153-197168394	MCF10A-Er-Src	breast:	n/a	n/a
10	GATA3	chr1:197168462-197168465	SH-SY5Y	brain:	n/a	n/a
11	HCFC1	chr1:197168459-197172025	Hela-S3	cervix:	n/a	n/a
12	JUND	chr1:197166714-197167569	K562	blood:	n/a	chr1:197167398-197167410
13	MAFK	chr1:197167403-197167412	K562	blood:	n/a	n/a
14	MAZ	chr1:197166551-197167191	K562	blood:	n/a	n/a
15	POLR2A	chr1:197167458-197168530	MCF10A-Er-Src	breast:	n/a	n/a
16	POLR2A	chr1:197168291-197168521	MCF10A-Er-Src	breast:	n/a	n/a
17	RCOR1	chr1:197166620-197167229	K562	blood:	n/a	n/a
18	STAT3	chr1:197166917-197167216	GM12878	blood:	n/a	n/a
19	STAT3	chr1:197167580-197167757	MCF10A-Er-Src	breast:	n/a	chr1:197167733-197167747
20	UBTF	chr1:197168577-197168724	K562	blood:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:197168091-197168141	NHBE	bronchial:	n/a
2	chr1:197168091-197168141	ProgFib	skin:	n/a
3	chr1:197168091-197168141	HEEpiC	esophagus:	n/a
4	chr1:197168091-197168141	HRCEpiC	kidney:	n/a
5	chr1:197168091-197168141	Jurkat	blood:	n/a
6	chr1:197168091-197168141	ECC-1	luminal epithelium:	n/a
7	chr1:197168091-197168141	Hepatocyte	liver:	n/a
8	chr1:197168091-197168141	HCPEpiC	choroid plexus:	n/a
9	chr1:197168091-197168141	GM19239	blood:	n/a
10	chr1:197168091-197168141	MCF10A-Er-Src	breast:	n/a
11	chr1:197168091-197168141	RPTEC	kidney:	n/a
12	chr1:197168091-197168141	CMK	blood:	n/a
13	chr1:197168091-197168141	PFSK-1	brain:	n/a
14	chr1:197168091-197168141	PANC-1	pancreas:	n/a
15	chr1:197168091-197168141	HMEC	breast:	n/a
16	chr1:197168091-197168141	HCF	heart:	n/a
17	chr1:197168091-197168141	HEK293	kidney:	embryo
18	chr1:197168091-197168141	AoSMC	blood vessel:	n/a
19	chr1:197168091-197168141	SK-N-SH	brain:	n/a
20	chr1:197168091-197168141	Hela-S3	cervix:	n/a
21	chr1:197168091-197168141	GM06990	blood:	n/a
22	chr1:197168091-197168141	SK-N-MC	brain:	n/a
23	chr1:197168091-197168141	A549	lung:	n/a
24	chr1:197168091-197168141	IMR90	lung:	fetal
25	chr1:197168091-197168141	HCM	heart:	n/a
26	chr1:197168091-197168141	HepG2	liver:	n/a
27	chr1:197168091-197168141	NB4	blood:	n/a
28	chr1:197168091-197168141	NH-A	brain:	n/a
29	chr1:197168091-197168141	HRPEpiC	eye:	n/a
30	chr1:197168091-197168141	GM12891	blood:	n/a
31	chr1:197168091-197168141	H1-hESC	embryonic stem cell:	embryo
32	chr1:197168091-197168141	T-47D	breast:	n/a
33	chr1:197168091-197168141	HL-60	blood:	n/a
34	chr1:197168091-197168141	HPAEpiC	pulmonary alveolar:	n/a
35	chr1:197168091-197168141	ovcar-3	ovarian:	n/a
36	chr1:197168091-197168141	U87	brain:	n/a
37	chr1:197168091-197168141	HCT-116	colon:	n/a
38	chr1:197168091-197168141	HRE	kidney:	n/a
39	chr1:197168091-197168141	HIPEpiC	eye:	n/a
40	chr1:197168091-197168141	HAEpiC	amniotic membrane:	n/a
41	chr1:197168091-197168141	K562	blood:	n/a
42	chr1:197168091-197168141	NHDF-neo	bronchial:	n/a
43	chr1:197168091-197168141	GM12892	blood:	n/a
44	chr1:197168091-197168141	NT2-D1	testis:	n/a
45	chr1:197168091-197168141	AG09309	skin:	n/a
46	chr1:197168091-197168141	SKMC	muscle:	n/a
47	chr1:197168091-197168141	AG09319	gingival:	n/a
48	chr1:197168091-197168141	SAEC	small airway:	n/a
49	chr1:197168091-197168141	Caco-2	colon:	n/a
50	chr1:197168091-197168141	SK-N-SH_RA	brain:	n/a

(count:10 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:197114016..197117152-chr1:197163839..197167436,4	K562	blood:
2	chr1:197153884..197156331-chr1:197167263..197169035,2	K562	blood:
3	chr1:197159273..197161304-chr1:197164955..197167252,3	K562	blood:
4	chr1:197165634..197167836-chr1:197312237..197315122,2	K562	blood:
5	chr1:197165132..197167397-chr1:197181290..197183417,2	K562	blood:
6	chr1:197110180..197113762-chr1:197163844..197167381,3	K562	blood:
7	chr1:197152680..197155309-chr1:197165847..197169413,3	MCF-7	breast:
8	chr1:197161517..197163826-chr1:197164890..197167674,2	K562	blood:
9	chr1:197112577..197117711-chr1:197168565..197172597,7	K562	blood:
10	chr1:197167660..197168424-chr7:117707343..117708112,2	MCF-7	breast:

No data

Variant related genes	Relation type
CRB1	TF binding region
CRB1	CpG island
ENSG00000066279	chromatin interactions

Extended variants
information (count: 51 )
Associated
traits (count: 87 )

Variant overlapped rSNPs/rCNVs (count:51 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs35972862	chr1:197167195-197167196	Flanking Active TSS Active TSS Enhancers Weak transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs147147256	chr1:197167271-197167272	Active TSS Weak transcription Flanking Active TSS Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs575484163	chr1:197167318-197167319	Active TSS Weak transcription Flanking Active TSS Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs550314239	chr1:197167320-197167321	Active TSS Weak transcription Flanking Active TSS Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs545931665	chr1:197167351-197167352	Active TSS Weak transcription Flanking Active TSS Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs139613117	chr1:197167370-197167371	Active TSS Weak transcription Flanking Active TSS Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs564156122	chr1:197167379-197167380	Active TSS Weak transcription Flanking Active TSS Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs572903688	chr1:197167391-197167392	Active TSS Weak transcription Flanking Active TSS Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs555237309	chr1:197167425-197167426	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs72333228	chr1:197167431-197167432	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs375839063	chr1:197167439-197167440	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs377186668	chr1:197167444-197167445	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs12402465	chr1:197167465-197167466	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
14	rs561485097	chr1:197167473-197167474	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs529594539	chr1:197167517-197167518	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs550963135	chr1:197167524-197167525	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs562756157	chr1:197167525-197167526	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs143890486	chr1:197167536-197167537	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs551485798	chr1:197167570-197167571	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs566621084	chr1:197167573-197167574	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs533982029	chr1:197167583-197167584	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs16841219	chr1:197167598-197167599	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs150647570	chr1:197167628-197167629	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs555905512	chr1:197167656-197167657	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs374582051	chr1:197167679-197167680	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs35245280	chr1:197167717-197167718	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs16841220	chr1:197167797-197167798	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs556943288	chr1:197167870-197167871	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs372580069	chr1:197167988-197167989	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs139808865	chr1:197168092-197168093	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
31	rs115273101	chr1:197168176-197168177	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs546238527	chr1:197168177-197168178	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs10494748	chr1:197168178-197168179	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs376169221	chr1:197168201-197168202	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs534912284	chr1:197168214-197168215	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs10494749	chr1:197168233-197168234	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs149818561	chr1:197168244-197168245	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs10494750	chr1:197168266-197168267	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs113827164	chr1:197168348-197168349	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs370656278	chr1:197168372-197168373	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs573521481	chr1:197168400-197168401	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs145837128	chr1:197168408-197168409	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs562355728	chr1:197168431-197168432	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs139752352	chr1:197168434-197168435	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs371859979	chr1:197168485-197168486	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs375291377	chr1:197168487-197168488	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs368942674	chr1:197168491-197168492	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs551547856	chr1:197168533-197168534	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs560274790	chr1:197168534-197168535	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs199584754	chr1:197168556-197168557	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:87)

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
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
Myelofibrosis	22110671	CNVD
Breast cancer	16272173	CNVD
Mental retardation	21062444	CNVD
Liver carcinoma	19366792	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Chordoma	18071362	CNVD
small cell lung cancer	20016488	CNVD

Chromatin state (count:278 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:197116600-197169800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr1:197125400-197168400	Weak transcription	Psoas Muscle	Psoas
3	chr1:197125600-197169600	Weak transcription	Esophagus	oesophagus
4	chr1:197126400-197169600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
5	chr1:197152400-197168600	Weak transcription	Stomach Mucosa	stomach
6	chr1:197157400-197168400	Weak transcription	Left Ventricle	heart
7	chr1:197157400-197169400	Weak transcription	Colonic Mucosa	Colon
8	chr1:197157400-197169600	Weak transcription	Pancreas	Pancrea
9	chr1:197157600-197167600	Weak transcription	Primary hematopoietic stem cells	blood
10	chr1:197159400-197169600	Weak transcription	Gastric	stomach
11	chr1:197159400-197169800	Weak transcription	Lung	lung
12	chr1:197159600-197167800	Weak transcription	Skeletal Muscle Male	skeletal muscle
13	chr1:197159600-197168600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
14	chr1:197159600-197169200	Weak transcription	H9 Cell Line	embryonic stem cell
15	chr1:197159600-197169800	Weak transcription	Spleen	Spleen
16	chr1:197159800-197168600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
17	chr1:197159800-197169600	Weak transcription	Primary neutrophils fromperipheralblood	blood
18	chr1:197160600-197167200	Weak transcription	Fetal Intestine Large	intestine
19	chr1:197160600-197169200	Weak transcription	Fetal Stomach	stomach
20	chr1:197161000-197167400	Weak transcription	Fetal Muscle Leg	muscle
21	chr1:197161000-197168200	Weak transcription	Fetal Thymus	thymus
22	chr1:197161000-197169200	Weak transcription	Fetal Muscle Trunk	muscle
23	chr1:197161000-197169400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
24	chr1:197161000-197169400	Weak transcription	Placenta	Placenta
25	chr1:197161200-197168600	Weak transcription	Primary B cells from peripheral blood	blood
26	chr1:197161600-197168800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
27	chr1:197162800-197167200	Enhancers	Primary T helper cells fromperipheralblood	blood
28	chr1:197163400-197169400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
29	chr1:197163600-197168800	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
30	chr1:197164000-197168600	Enhancers	Primary T helper naive cells from peripheral blood	blood
31	chr1:197164000-197168800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
32	chr1:197164000-197169200	Active TSS	GM12878-XiMat	blood
33	chr1:197164600-197168400	Enhancers	Hela-S3	cervix
34	chr1:197164800-197167200	Enhancers	Primary T killer memory cells from peripheral blood	blood
35	chr1:197164800-197169400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
36	chr1:197165000-197169400	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
37	chr1:197165600-197169200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
38	chr1:197165800-197167200	Enhancers	Small Intestine	intestine
39	chr1:197166200-197167400	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
40	chr1:197166200-197167600	Active TSS	Ovary	ovary
41	chr1:197166200-197170000	Flanking Active TSS	Dnd41	blood
42	chr1:197166400-197167200	Enhancers	Sigmoid Colon	Sigmoid Colon
43	chr1:197166400-197167200	Enhancers	HSMM	muscle
44	chr1:197166400-197167600	Active TSS	HUES48 Cell Line	embryonic stem cell
45	chr1:197166400-197168000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
46	chr1:197166400-197168400	Active TSS	Brain Anterior Caudate	brain
47	chr1:197166400-197168600	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
48	chr1:197166400-197171400	Active TSS	K562	blood
49	chr1:197166400-197171600	Active TSS	HUES6 Cell Line	embryonic stem cell
50	chr1:197166400-197171600	Active TSS	Right Atrium	heart

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