EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS194-01370 
Organism
Homo sapiens 
Tissue/cell
Urothelial_cell 
Coordinate
chr14:65192360-65194310 
TF binding sites/motifs
Number: 4             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
NOTOMA0710.1chr14:65192365-65192375GCTAATTAGC+6.02
NOTOMA0710.1chr14:65192365-65192375GCTAATTAGC-6.02
RELAMA0107.1chr14:65193442-65193452GGGAATTTCC+6.02
ZEB1MA0103.3chr14:65194220-65194231CCCACCTGCCC+6.14
Number of super-enhancer constituents: 29             
IDCoordinateTissue/cell
SE_03251chr14:65192192-65193789Brain_Angular_Gyrus
SE_03953chr14:65190319-65195292Brain_Anterior_Caudate
SE_04856chr14:65180505-65197762Brain_Cingulate_Gyrus
SE_05821chr14:65180438-65199821Brain_Hippocampus_Middle
SE_06781chr14:65192065-65195493Brain_Hippocampus_Middle_150
SE_07938chr14:65190169-65194504Brain_Inferior_Temporal_Lobe
SE_19856chr14:65188989-65195748CD4p_CD25-_Il17p_PMAstim_Th17
SE_20478chr14:65185982-65194236CD56
SE_22874chr14:65186008-65194196CD8_primiary
SE_23289chr14:65190472-65194123Colon_Crypt_1
SE_24426chr14:65191797-65193408Colon_Crypt_2
SE_24426chr14:65193426-65194045Colon_Crypt_2
SE_26750chr14:65181719-65194103Esophagus
SE_27717chr14:65189231-65195032Fetal_Intestine
SE_28783chr14:65190366-65194949Fetal_Intestine_Large
SE_32308chr14:65191832-65193491Gastric
SE_36148chr14:65181584-65194566HMEC
SE_47632chr14:65192885-65193854Pancreas
SE_49272chr14:65190395-65192755Right_Atrium
SE_50477chr14:65190429-65195289Sigmoid_Colon
SE_57093chr14:65190453-65193416VACO_400
SE_57093chr14:65193490-65194055VACO_400
SE_57603chr14:65191845-65193429VACO_503
SE_57603chr14:65193483-65194199VACO_503
SE_57932chr14:65192783-65193254VACO_9m
SE_57932chr14:65193561-65193963VACO_9m
SE_64475chr14:65185799-65194369NHEK
SE_65298chr14:65181865-65199543Pancreatic_islets
SE_68953chr14:65192622-65194088H9
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr146519342265193546
Number: 1             
IDChromosomeStartEnd
GH14I064714chr146518085865194899
Enhancer Sequence
ATCCTGCTAA TTAGCCCTCT GGGCATTGCA CTGGGCTGCG GAGGGGAGCA CTGGGCTGCC 60
ACTGAGTCCC CATCTGCAAG TTGAGAGGCT CATACAGAGC TCCTTGGAGG TGACCCCCTC 120
CAGTGAGACA CAGTGACAAA GTGCTGTGCT CCAGAGCATC CCGGCCAGGT TAGCGGCAGG 180
TGGTAAGTAG GTCTTGAGGC GCTTGATCTG TACCTCAGTA AAAGCATCAG TTTGTTCACC 240
ATTGTTGTTC ATTTGTTAAA TTGGCCCTTA AGACCCCTGC TTTTTAGTAA CTAATGGTGT 300
AGGGCAGAGG GTCTCAAACT AGTCACACTG TCTCAGGCCA GTGCTACAGT AGGAGAAACC 360
TGGGAGGTAG TAAGAGAACA CAGAAAGAGT TCCCCAGGTT TGGGGGATAT TGGAAGGTTC 420
CTGGAGGGGG CGATGTCTAA TTGGAGACCT AAAGATTGGA TGTAAATTAC ATAGGTTGGG 480
GGATGGTACT GTATGGGGTG GATGGGGACG AGATAACGCC AAGGCAGAGA GAACATTTGC 540
AAAAGCCGGA GACCCAGGGG TGTTGGTTTC CAGGTTGAGG CATAGGCACA GAAAACCAGG 600
GGTCAGTGTC AAGGGTTCCC AGAGTAATGG CAGCTTCTAG ATTCTTCTCC TTGTAGCTCA 660
AGTCTCTGCC CTTTAGTCAT GTCTGGGGTC TAGTCACTTC TGAGCCCTAG AGCTAGGGGT 720
AGAAGACTCG GGTCAGTAGG GGTGAGAGGG ATGCCCAGGA ACTTACTGTT TTCCTGTGAA 780
ATAGCAATGA AATGTGTACT CTGCAAAGTG GCATTGGTGA GCTCTAAGGG GTGGGCATGG 840
GTGTTGCATG GGTGTCCCTG TCCTTCCCAA AGGCTGCAGC CTGAAGTAGT CTGGCCACTC 900
CACCCTTCCA TCCCCCGGCT GCTCCAGGTG GGCCTGCCTG TGAGCCACAC CATCTGCTTT 960
GGGAATAAAG TCCACCTGAG GCTCTGTTTG CCTCACCTGG GTGCAGTTTA CTGCTTTCTC 1020
TGCTGCCCCC GCCCAGCTGT GCCAAGGGGA GCTTACAGAG ACTCACTGAT GGCTTAGCCC 1080
TGGGGAATTT CCTGGGGCCT GGGATGAGTC AGAGGCAGCC TGTACCAGGT GCTGGGGTGG 1140
GGCTGCGGAG TCGGGGGATA ATGCTGGCTC AGCCAGTCAG TATCCAGAAA GTTTCAGGTT 1200
TGTGGTGAAG CCGCCGGTGC CCCTGAGGTT TTGCAGTCTT AGGGAGAATA TTACCCCTGT 1260
TATGTGTCTT GTCTTAACAT TGTAAGAACC AGATCTTTGC CCATCCCTGT ACAGTGACCC 1320
CAGCACAGGC CACAGACAGG GGGGCACTTG GGAAGTTCTT CTTCACAACT GCCATTATTA 1380
TCACCATATT GATGGTGTAT GGAGCACGTA CCCTATGCCA GGCATCATGC TCAGAGCTTT 1440
ACGAACAGCA GGTGGCTTCA TCTGGGAGGA CACAGCCATG GGGTAGGCTG TATCCATCCT 1500
CATTTTACAG GTGAGGAGCT GAGGCTCTGA GGGACTAAGT ACTGTGCCCC AGCAGTGGGG 1560
CTGGGCTGTG AATTCCTTAG AGGGTACCTG GACCACTGTG CTGGCAGGTG GACTTGGGCA 1620
CCCTCATCAG TGCTCATAGA GTCTGAGAAC AGGGCCCTTC TTGGGATTCA GTTTTGTTTT 1680
GTTAATTGTG TTAAATGTAA ATACACATAA CATAAAATTT ACCATCTTCA CCATTTTAAG 1740
TGTACAGTTC AGTGACAGTA GGTACATTCA TATCATTGTG CAATGTCATC ACTGTCTATC 1800
CACAGAACCT TTTCATCTTC TAAAACTGAA CTCTGGATGC ACTAAATAAT ACCTTCCCAC 1860
CCCACCTGCC CCCACCCCTG GCAACCGTCC CTCTGTTCTG TTTCTGTGGG CATTCAGAGG 1920
TTGACCCTTC ATCTGTCTGT CTTGTTGCAG 1950