EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS177-24330 
Organism
Homo sapiens 
Tissue/cell
SK-N-SH_RA 
Coordinate
chr9:137257600-137259130 
TF binding sites/motifs
Number: 2             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
ESX1MA0644.1chr9:137258868-137258878GTTAATTGGT-6.02
ZNF740MA0753.2chr9:137258150-137258163CCACCCCCCCCAT+6.46
Number of super-enhancer constituents: 30             
IDCoordinateTissue/cell
SE_00174chr9:137256755-137259829Adipose_Nuclei
SE_00860chr9:137255901-137260558Adrenal_Gland
SE_02933chr9:137257000-137258918Bladder
SE_05812chr9:137248771-137260982Brain_Hippocampus_Middle
SE_09174chr9:137254160-137271835CD14
SE_23121chr9:137257215-137258962Colon_Crypt_1
SE_23757chr9:137257477-137258890Colon_Crypt_2
SE_24707chr9:137255976-137259679Colon_Crypt_3
SE_26524chr9:137256603-137261031Esophagus
SE_28276chr9:137255240-137260623Fetal_Intestine
SE_29238chr9:137255536-137260979Fetal_Intestine_Large
SE_31436chr9:137257235-137259271Gastric
SE_33498chr9:137255830-137262370H2171
SE_34123chr9:137257219-137258975HCC1954
SE_34906chr9:137257194-137259877HeLa
SE_40986chr9:137256096-137259621Left_Ventricle
SE_41556chr9:137243649-137273607LNCaP
SE_42130chr9:137254678-137260854Lung
SE_43440chr9:137245134-137261072MCF-7
SE_47617chr9:137257494-137258929Pancreas
SE_48050chr9:137252285-137278501Psoas_Muscle
SE_49423chr9:137256346-137259249Right_Atrium
SE_50152chr9:137256575-137259121Sigmoid_Colon
SE_51460chr9:137256881-137259251Skeletal_Muscle
SE_52424chr9:137256233-137259619Small_Intestine
SE_53315chr9:137256820-137259081Spleen
SE_54834chr9:137256437-137259599Stomach_Smooth_Muscle
SE_65247chr9:137243550-137260818Pancreatic_islets
SE_68695chr9:137256582-137258009H9
SE_68695chr9:137258952-137260384H9
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr9137257724137257990
Number: 1             
IDChromosomeStartEnd
GH09I134363chr9137255386137260783
Enhancer Sequence
GCTGTCGGTG GGTGAGGTGC CCCAGGGGAA GGGAGGGCCA GCCCAGAAGG ACCCTCCCAT 60
TACCCTCTGG TGGCTTGCCC ATGCCACCAT TCCTACTGCT AGGCTCAGGC CTGTCTTGGG 120
GAGGGTTCCT GGGCTGGGAT TGGCCGTCGG GGAGGTGCAC ACAGACGCTC AGCACAGTTG 180
TGGCTGCCTC CAGTCAGGCG TCCGCTGAGC GACCCCTAGG AGCCGCCTGT CTTTGCAGGA 240
GCCGCGGGGA TCATCTGGCG GCTGCCTCCA CCCCTGCCTC CACCCCTCCC TTTTTGGGAG 300
GTGGGGCTTG GCATCTTCAG CATCTCTCGT GCCTCAGTAA CAACCTGGGA GCGGTGCTGT 360
CCCTGGGTAC AGATGAGAAG CCAAGGCTCA GAGGCACCAG GGCCCCAGTG GGAGGCGGCA 420
GAGCCTCTGG TGGCTCCGTG TGGCATGTTC TGGGCTGTGT GTGGGGCCAG GGAGGGTGTC 480
TTCAGCACAG GTGCCCGCTG GGTGGTCTCC CATGTGTGCC CAGGAGGAGT GCCACAGCCT 540
CTCCCTCTGC CCACCCCCCC CATGCCTGCC CTGCCAGCAG GTCCAGCAGG CCTTGGCACA 600
GGCTCCAGAA TTGCACGTGA TCTCAGACGG TTCCCAGCTT CCTCTGCAGG GCGGGGCTGC 660
TCCAGTCTCT TACACCAGCG CATCTGCAAC TCATTACACA GCGGTGTCGG TGGCAGAGTG 720
GCCTGGCCAC GGCGAGCTCC TGGCGGGAGT CCCCCTCCCC AGCAGCCACC CCGTGCCATG 780
GGCCTCCAGG TCCCCCGGGT GCTGGCCTGG GGACAGCACC ACAGGGCCCA GCCAGGGCTG 840
GGGCAGGGAG GAAGGGCCCC TCCACTAGTG GGCTTTGGCC TCCTCGTGAG GAGCTGGGTG 900
GGGCTGGAGA AATCAGCTCC CGCCAGCCTG ATCTTCCTGC CTCAGAAGCT GAACCCCGGG 960
GACAGTGTTG GTCAGAAAAG CCATAGACTC TCCACGGAAA AGGAAGCCTG GCACCCCCCA 1020
TGTTTCACGT AGGCCACCCT AAGGTCCACA GATGCCTGGG GACAAGGATT AGTGTGAGCA 1080
AAGACACAGG AGTCGGGGAC ACATCCCAGT CGGAACGTGG TGGAAAGGCG CCAGGCAGGC 1140
TGAGTCGGAG ATGTCCCTCA GGCTCCTGCT GGGAGAAGGG GCTGGTGGTT CCCGGGCCTG 1200
CACATCCCCA CCCCTGCCCT GCGTGCCACT CTCAGCCTTT GCCCAGCACC AGGCTTATTA 1260
TCCGATTGGT TAATTGGTTG AGATACGGGT CACCTCCCGT AACAGTCATC TTTTTAAGGC 1320
GTGCAGTTCA GTGGGTTTTC ATCCACACAC TTGCACAGCC ACCACCACAG CCAGCTTTAG 1380
AATTTCGAAG CACTTCCACC AACCCCCCAA AAGAAGCCCC GTGCCCGCTG GAGCTGCTGC 1440
AGTGCCCCGC CTGACCCCAC CAGCCACTCC CCTGCCTGCC TTCTTTGTGG ATCTGCCTGG 1500
TCTGGCGTTT GTGATCTCCC TCCATCTTCA 1530