EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS098-56383 
Organism
Homo sapiens 
Tissue/cell
HSMM 
Coordinate
chr8:134306320-134307470 
TF binding sites/motifs
Number: 6             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
MAFFMA0495.3chr8:134306693-134306708ATGCTGAGTCATCAC-6.63
MAFFMA0495.3chr8:134306693-134306708ATGCTGAGTCATCAC+6.64
NFE2L1MA0089.2chr8:134306692-134306707GATGCTGAGTCATCA-6.47
Nfe2l2MA0150.2chr8:134306694-134306709TGCTGAGTCATCACG-6.75
Sox3MA0514.1chr8:134306430-134306440AAAACAAAGG-6.02
ZNF740MA0753.2chr8:134306914-134306927GGGGGGGGGGCAG-6.33
Number of super-enhancer constituents: 25             
IDCoordinateTissue/cell
SE_00425chr8:134301340-134311366Adipose_Nuclei
SE_03285chr8:134306114-134307169Brain_Angular_Gyrus
SE_03285chr8:134307354-134309528Brain_Angular_Gyrus
SE_04229chr8:134301793-134311272Brain_Anterior_Caudate
SE_04976chr8:134295645-134311554Brain_Cingulate_Gyrus
SE_05911chr8:134295053-134311486Brain_Hippocampus_Middle
SE_07206chr8:134302445-134311277Brain_Hippocampus_Middle_150
SE_07895chr8:134295546-134311683Brain_Inferior_Temporal_Lobe
SE_09628chr8:134301461-134311725CD14
SE_19655chr8:134305278-134311331CD4p_CD25-_Il17p_PMAstim_Th17
SE_24176chr8:134305824-134307346Colon_Crypt_2
SE_26786chr8:134301474-134311822Esophagus
SE_27791chr8:134300251-134313000Fetal_Intestine
SE_28981chr8:134300073-134313069Fetal_Intestine_Large
SE_31524chr8:134300227-134311122Gastric
SE_35245chr8:134304945-134311975HeLa
SE_36421chr8:134305230-134312008HMEC
SE_41455chr8:134299416-134311207Left_Ventricle
SE_42343chr8:134299449-134311251Lung
SE_49373chr8:134301634-134311208Right_Atrium
SE_50820chr8:134301340-134311288Sigmoid_Colon
SE_52812chr8:134301376-134312556Small_Intestine
SE_65084chr8:134305754-134311208NHEK
SE_65489chr8:134304326-134310961Pancreatic_islets
SE_67840chr8:134304577-134311557u87
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr8134306455134306820
Enhancer Sequence
ATGTCTGTTA CTCTCATTTT ACAGAAAAGC AAACTGAGGC ATGGAGCTCC TGACTGCCTT 60
TTCATTTGAG CCTGATTTCT TCAGGCGCCC CAACATGTTG TCATGGAAAA AAAACAAAGG 120
CTCTGAAGTC CAACTGTCCG GGTTCAAAGT CTGGCTCTCC CACCTGAGCC ATATGGCAAC 180
AGGCAAATCC TGAAACTCTC CTGGCCTCAG TTGCCTCATC CATTCAATGG AGCAATACGA 240
TCCAGGCAAC GTTCTTGCGA GGATGAAGGC AGATGGAGGG AGACAGTGGC TGCTCTGGAG 300
GGAGAGAGAT GTCGTGTCCC TCCCTGGCCT TCCTTCCAGG CTGAGTCAAA CCTGAACCCT 360
GCTTGAGTCT CAGATGCTGA GTCATCACGC TTTCTCTCCC AGGACAAGGC CTCTGAGTCA 420
CATCTGGAAT GGGATTCTCT GGGGTTGGGT CCCAAGGAAG AACTGCAGCT TTGGGCCACC 480
CGAAAAACAC AATGCTATCT TTCTTTCAGG TCCATGAGGA GGCAAGTTCA GGCCAGCGGA 540
TTTCAACGTA ACCCAGGGGG GCCCTCAGCT CAGTTGAGAT CTGTCTTCTG TCATGGGGGG 600
GGGGCAGCCC CATTCAGTCA AAGGCCAACT CAGGGGGCTG CAGCCTCTAA GCCCCTGCCC 660
TTCAGGCTGG CTTTGCTAAT CTCTCAAGAA CACCTGATTT ACACTTAAAA AAAATCATTC 720
CGCTCTGCCC CTTTGGCCTC AAAAGTTTCC TCACCAGAAA TTCAATGAAG ATGCAATTTC 780
CTTTCGCCCC TCCATAGCAG GCAGGCAAAA TCCTGCCAGG AACCCTTTCC ACTGCCTTCA 840
GTCCCACCCA GGAGCCTCTC ACAAAGCTGA GCTCCAGCTC AGTTCGGCCT GGGCACATCC 900
CTCCCCATCC CTGTGCCTCA TTTTCCATCT GTAAAATGGA AAGAAGTTGG ACTAGGTAGG 960
TCCTGTGTGA GTTTTTTATT CCATTCCAAA TGATCAAACT TTGTTGCTCC AAAAGAACTT 1020
CCTCACAAGA GACCCAAACA GACACTCCAG GATCCCTCAA AAGCAAAAGC CAACACCTCC 1080
ACCCATGCAC AGTCTATTAC CTCGCCCGAA ACTCAACCTG CTGGTTCACA GGAGAATGGG 1140
GCAGAAGACC 1150