EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS129-11726 
Organism
Homo sapiens 
Tissue/cell
MCF10A 
Coordinate
chr14:65191670-65194010 
TF binding sites/motifs
Number: 6             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
NOTOMA0710.1chr14:65192365-65192375GCTAATTAGC+6.02
NOTOMA0710.1chr14:65192365-65192375GCTAATTAGC-6.02
RELAMA0107.1chr14:65193442-65193452GGGAATTTCC+6.02
RREB1MA0073.1chr14:65192090-65192110GGGATGGTGGTGGTGGGTGG-6.68
RREB1MA0073.1chr14:65192097-65192117TGGTGGTGGGTGGGTGGGGT-8.17
SOX10MA0442.2chr14:65191704-65191715TGCTTTGTTTT-6.02
Number of super-enhancer constituents: 32             
IDCoordinateTissue/cell
SE_03251chr14:65190497-65192006Brain_Angular_Gyrus
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_06781chr14:65180403-65192060Brain_Hippocampus_Middle_150
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_54434chr14:65191114-65192192Spleen
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: 2             
ChromosomeStartEnd
chr146519171865193014
chr146519342265193546
Number: 1             
IDChromosomeStartEnd
GH14I064714chr146518085865194899
Enhancer Sequence
AGAGCGCTCA GAGCATTTCA GCAGTTGGCT GTTATGCTTT GTTTTAGCCT TAGGAGATAG 60
GAGCTTAGTT TGCAGACAGG TAGCCTATGA TCAATCAGAG AGAAAACTTC TGTAAGTAGA 120
AAAGACATAT TAGTTTCTGG GTTTGAAGTG TGCTTATGTT GCTATCCTCT TACAGTGGGA 180
TCCCCAGAGA GGGACCCTCA AAAGGTCCCT TTTAGAGACA AATCTCCCTA ATGGTGTGTG 240
TGTTGGGGTA GGGGTGGGGC TGTGAGTAAT CTTTTGCTTT AAGACTGTGA ACTGGCTGGC 300
TGTGAAATCC ATTTGGGAGT GGGGCCGTTT CCATTTAGCT TCCCCAGAGA AGCTGACTGA 360
CCCCAGATGT GATCTGGGAA AGGTCTTAGG CTGTAAATCC CTGCCCCTTT GTTCCCTGCT 420
GGGATGGTGG TGGTGGGTGG GTGGGGTGCC TAACTGCAGT GCACTTTGAA GGACATCAGA 480
GTGCCACAGG GCTGGGGGTT AAGGGCTGGG GTGGAGCTTG GGTTTTTATC TGTCAGTGCT 540
GGAATGACAT GGTGTTGCCC TGCCTGCTGG TTCTGTAAAA GGCATAGCTG ATTAATTGTA 600
AAGGCCCTTT TGAGGAGGGA GGAAAAAGCA ACAGCCCTAC AATTCCCAGG GGGCTCTCTT 660
CTGAGCAGCT CAAAGAGCTT TACCAAAATG ATCCTGCTAA TTAGCCCTCT GGGCATTGCA 720
CTGGGCTGCG GAGGGGAGCA CTGGGCTGCC ACTGAGTCCC CATCTGCAAG TTGAGAGGCT 780
CATACAGAGC TCCTTGGAGG TGACCCCCTC CAGTGAGACA CAGTGACAAA GTGCTGTGCT 840
CCAGAGCATC CCGGCCAGGT TAGCGGCAGG TGGTAAGTAG GTCTTGAGGC GCTTGATCTG 900
TACCTCAGTA AAAGCATCAG TTTGTTCACC ATTGTTGTTC ATTTGTTAAA TTGGCCCTTA 960
AGACCCCTGC TTTTTAGTAA CTAATGGTGT AGGGCAGAGG GTCTCAAACT AGTCACACTG 1020
TCTCAGGCCA GTGCTACAGT AGGAGAAACC TGGGAGGTAG TAAGAGAACA CAGAAAGAGT 1080
TCCCCAGGTT TGGGGGATAT TGGAAGGTTC CTGGAGGGGG CGATGTCTAA TTGGAGACCT 1140
AAAGATTGGA TGTAAATTAC ATAGGTTGGG GGATGGTACT GTATGGGGTG GATGGGGACG 1200
AGATAACGCC AAGGCAGAGA GAACATTTGC AAAAGCCGGA GACCCAGGGG TGTTGGTTTC 1260
CAGGTTGAGG CATAGGCACA GAAAACCAGG GGTCAGTGTC AAGGGTTCCC AGAGTAATGG 1320
CAGCTTCTAG ATTCTTCTCC TTGTAGCTCA AGTCTCTGCC CTTTAGTCAT GTCTGGGGTC 1380
TAGTCACTTC TGAGCCCTAG AGCTAGGGGT AGAAGACTCG GGTCAGTAGG GGTGAGAGGG 1440
ATGCCCAGGA ACTTACTGTT TTCCTGTGAA ATAGCAATGA AATGTGTACT CTGCAAAGTG 1500
GCATTGGTGA GCTCTAAGGG GTGGGCATGG GTGTTGCATG GGTGTCCCTG TCCTTCCCAA 1560
AGGCTGCAGC CTGAAGTAGT CTGGCCACTC CACCCTTCCA TCCCCCGGCT GCTCCAGGTG 1620
GGCCTGCCTG TGAGCCACAC CATCTGCTTT GGGAATAAAG TCCACCTGAG GCTCTGTTTG 1680
CCTCACCTGG GTGCAGTTTA CTGCTTTCTC TGCTGCCCCC GCCCAGCTGT GCCAAGGGGA 1740
GCTTACAGAG ACTCACTGAT GGCTTAGCCC TGGGGAATTT CCTGGGGCCT GGGATGAGTC 1800
AGAGGCAGCC TGTACCAGGT GCTGGGGTGG GGCTGCGGAG TCGGGGGATA ATGCTGGCTC 1860
AGCCAGTCAG TATCCAGAAA GTTTCAGGTT TGTGGTGAAG CCGCCGGTGC CCCTGAGGTT 1920
TTGCAGTCTT AGGGAGAATA TTACCCCTGT TATGTGTCTT GTCTTAACAT TGTAAGAACC 1980
AGATCTTTGC CCATCCCTGT ACAGTGACCC CAGCACAGGC CACAGACAGG GGGGCACTTG 2040
GGAAGTTCTT CTTCACAACT GCCATTATTA TCACCATATT GATGGTGTAT GGAGCACGTA 2100
CCCTATGCCA GGCATCATGC TCAGAGCTTT ACGAACAGCA GGTGGCTTCA TCTGGGAGGA 2160
CACAGCCATG GGGTAGGCTG TATCCATCCT CATTTTACAG GTGAGGAGCT GAGGCTCTGA 2220
GGGACTAAGT ACTGTGCCCC AGCAGTGGGG CTGGGCTGTG AATTCCTTAG AGGGTACCTG 2280
GACCACTGTG CTGGCAGGTG GACTTGGGCA CCCTCATCAG TGCTCATAGA GTCTGAGAAC 2340