EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS091-24309 
Organism
Homo sapiens 
Tissue/cell
HepG2 
Coordinate
chr19:45942050-45944950 
TF binding sites/motifs
Number: 3             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
CTCFMA0139.1chr19:45942877-45942896GGGCCACCAGGGGGCGCGG+7.19
Foxd3MA0041.1chr19:45942452-45942464AAACAAACAAAC-6.32
MEF2BMA0660.1chr19:45943185-45943197GCTAAAAATAGT+6.11
Number of super-enhancer constituents: 40             
IDCoordinateTissue/cell
SE_01498chr19:45942833-45944111Adrenal_Gland
SE_02108chr19:45942659-45944793Aorta
SE_02406chr19:45942626-45944083Astrocytes
SE_03036chr19:45942873-45943894Bladder
SE_06640chr19:45942245-45944998Brain_Hippocampus_Middle
SE_09930chr19:45942427-45943956CD14
SE_11261chr19:45942250-45944562CD20
SE_12309chr19:45943141-45944010CD3
SE_14395chr19:45942417-45944510CD4_Memory_Primary_7pool
SE_16220chr19:45942579-45943820CD4_Naive_Primary_7pool
SE_16563chr19:45942537-45943950CD4_Naive_Primary_8pool
SE_17214chr19:45942536-45944077CD4p_CD225int_CD127p_Tmem
SE_19219chr19:45942438-45944101CD4p_CD25-_Il17p_PMAstim_Th17
SE_20014chr19:45942216-45944187CD56
SE_20748chr19:45942289-45944277CD8_Memory_7pool
SE_21766chr19:45942403-45943715CD8_Naive_7pool
SE_22333chr19:45942181-45944271CD8_primiary
SE_23143chr19:45942794-45943873Colon_Crypt_1
SE_23745chr19:45942805-45943742Colon_Crypt_2
SE_24769chr19:45942653-45943882Colon_Crypt_3
SE_26771chr19:45942658-45944815Esophagus
SE_29756chr19:45942465-45944778Fetal_Muscle
SE_31887chr19:45942664-45943954Gastric
SE_34472chr19:45942692-45944959HCT-116
SE_35967chr19:45942563-45943789HMEC
SE_38090chr19:45942414-45944040HUVEC
SE_39922chr19:45942598-45944765K562
SE_41239chr19:45942635-45944849Left_Ventricle
SE_44217chr19:45942733-45944784NHDF-Ad
SE_44830chr19:45942605-45944087NHLF
SE_45809chr19:45942415-45944792Osteoblasts
SE_47661chr19:45942791-45943591Pancreas
SE_48343chr19:45942343-45944744Psoas_Muscle
SE_49047chr19:45942813-45944746Right_Atrium
SE_50737chr19:45942718-45944750Sigmoid_Colon
SE_51420chr19:45942394-45944499Skeletal_Muscle
SE_52836chr19:45942665-45944567Small_Intestine
SE_53558chr19:45942445-45944250Spleen
SE_57973chr19:45942871-45943474VACO_9m
SE_65504chr19:45942507-45944327Pancreatic_islets
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 3             
ChromosomeStartEnd
chr194594212645942253
chr194594316345943490
chr194594240045942800
Number: 1             
IDChromosomeStartEnd
GH19I045439chr194594225945944857
Enhancer Sequence
CACCACGCCC GGCTAATTTT GTATTTTTAG TAGAGACGGG GTTTCTCCGT GTTGGTCAGG 60
CTGGTCTCGA AATCCCGACC TCAAGTGATC CGCCCCACTC GGCCTCCCGA AGTGCTGGGA 120
TTACAGGTGT GAACCACCGC GCCCGGCCCG AAGTTATTCC TCTTATCTGA CTGTAGTTTG 180
GTATTTTTTA ACCGCATCTC TCTGTTCTTC CTCTCCCAAC CCCATCTCTA CTAAAAATAC 240
AAAATTAGCC AGCCGTTGTG GCGCATGCCT GTAATCCCAG CTACTCGGGA GGCTAAGGCA 300
GGAGAATTTC TTGCACCCAG GAGGTGTAGG TTGCAGTGAG CTGAGATCGC ACCACTGCAC 360
TCCAGCCTGG GCGACAGAGC GAGACTCTGT CTCAAAAAAC AAAAACAAAC AAACAAAAAA 420
ACAAATAGCG CCTCGTTTTC TGGGAGGCAG TGAATTCCCC ATTTAGGAAG TGTCCAAGCT 480
CAAGTTGAAA TGATGGTACA TTGCGGTTCA TGCTGCAATG CCTCAACCCA GTTCCTCTCC 540
GGACCTCAGT TTCCTCATTT ATAAAATGGG TGTGGACGAC GAGGTCAGAT TTAAAAAAAT 600
AATAATAGTA GTTAATAATA ATAGGCCGGG TGCAGTGGCT CAGGCCTTTA ATCCCAGCAC 660
TTTGGGAGGC CGAGGTAGCA GGATCGCTTG AGCCCAGGAG TTCTAGACAA TCCTGGGGCA 720
ATATAGCGAG ATTCTATCTC AAAGAAATAA TCATAATCAT AATAAAAATA AATGAATAGA 780
TAAGCTGAGA CGGACTCAGG CCCAGCTCCT GCCTGCGATC CCTGCGGGGG CCACCAGGGG 840
GCGCGGCGCC CCTGCCCAAA ACTCCGCCGT CGGCTCTGAA CCCCGGCGGA CGCGTCCCGA 900
CGCCCCTGGA AGATTCTGCG CCCTGCCGGC TCGCCGGCGC CCGGGAGCCC GGGAGGCGGG 960
TGTGCACGCG GGGTGTCCAG GGCGCCCCCG ATCGAGGCCC CCTCGCCGTG CCTCGGGGTA 1020
GGGGGACGGC TGTGACTCAG GCGCGCGCTC CTCCCCGGGG CCCTCAGTGG TCGCGAGGGG 1080
GCGCGCACGG CCTCGGGAAC CCGCGCGGCG CCGCGTCCAT TTTTACCCCA GCTCCGCTAA 1140
AAATAGTTGC CGCGCTCCGA GCCGAGCCCG AAATAGCGGC CCCCAGATAA GGCAGGACGA 1200
CTCAGCGCTT CCGGGGAGCG GAAGGGGGAG CGCGCGGGGG GAGCGGTGCT GGGCGCAGCC 1260
CGGCCGAGCA GGCGCCGCTG TCCCCAGCGC ACCCCCACTC TGCCCTGGCG GTCACACTCG 1320
CCCCCGACTG CGACCCCGCC CCGCCGCTAG CCTGGCTGCC TTCCTACGTC CCCCACATTG 1380
TATCCTCATC CCCTGTCCCC CATCCTCAGC TTCACCTCCA TTCCTCATCA TAACTCCCCC 1440
CTCCCCTACA CCCCCAGCGA TGTCCCCCAC TGGTACTCAT CCGCATCCCC CAGCCTGTCC 1500
TACTCCTGTC CCTATTTCCC CTCTCCACCC TCATCGCCAA TCTCCTGTCG TCCTGAATCT 1560
GCCCCTTACC ATCTCTGTCC TCAAGGCCAA CCTTTATGGG GGCAGAGCAG GGCGAGAGGA 1620
TCACAGGGAG TCAGGAGACC TGCGGGCTGA GGGCTGAGGG CTGGGGGTGA GGATCTGATT 1680
TCTTGGTTTG TTTCTACTGT GGGCAGGGGT AGGCTTAGAT CTGGGGGTTG GAGCATGGGA 1740
CACTTCAGTC TGGCCTAGTC TTCAGAGCTG AGGCGAGGCA TGGCCAGCAT CACGGCTCAT 1800
TCTGTGACCA GGGTCGGGGC TCAGGCTGGG GAAGGATGAC CGTCTTTGTC ACCAAATTTG 1860
ATCACTGTGT CACCAGAGTT AGGGCTCAGC CTTGAGCCGT TTCTTTATTT ACCCACCTCC 1920
ACTAATATTT TTTATTTCAG ACAAGGCCTT GCTCTGTCGC CCAGGCTGGA GTGCAGTGTT 1980
GCCCATGCTG GAATGCAGTG CTGGGATCTT AGTTGACTGC AGCCTTGAAC TCCTGGGTTC 2040
AAGAGATCCT CCCACCTCAG CCTTCCTAGT AGCTGGGACT ACAGGTGTGC ACCAGCACAC 2100
CTGGCTAATT TTTCATTTTT TTGTAGAGAC AGAGTCTCCA TGCCTTGCCC GCCTTGTCCA 2160
GGCTGGTCTT GAGCTCCTGG CCTCAAGCTA TCCTCTGGCC TCCTCCTAGG AAGGCACTGA 2220
AATGACAGGC ATGAGCTACA GAGCCCGCCT CCACTAAGAT TCTTTCCTCC CTTGCAAGTC 2280
AGTGATTGGA CACAACAGCT CCAGGCCTTG GGAACAGTCA GAACTCTGTT CCCTGGGCCT 2340
AGGTCTTCCC TTTGCACTGA GATCATCTAA GGGCCTCCCC ATTTCCATAT CCTGAGATTC 2400
TCAGTGCCCA CTCCAAGCAT CAGTGTCAGG CCTCAAGGAC CTACACTGCA TGTTCTGGGG 2460
GTTTAAAGGG AGCACACTGA CTTCCCTGAG GGTGACAGAG GTCAGAATGA GTGACTAAGG 2520
TCTTGGGCCT GGCCCTGACC CTGCAGTGGG TGGGAGAGAT ACCCAGTTGA GGCCCAGGTC 2580
TCCACCCAGG TAGCAGGGTG GATGGCGGGG GGGTCATCCC TGAGGTGAAA TGTGGGTGGA 2640
AGATACCTAG ATAAGTTTCA GAGTCAGTGC AGAGATGGTA ATTTTTAAGT AACTTCTAAA 2700
ATTTTCGAGT AGCTGGGATT ACAGGCGCCT GCTACCAAGC CTGGCTAATT TTTGTATTTT 2760
TTTGTAGAGA CGGGGTTTTA CTATGTTGTC CAGGCTGGTC TCAAACTCCT GACCTCAAGT 2820
GATCCGCCCA CCTCGGCCTC CCAAAGTGCC GGGATTACAG GCGTAAGCCA CTGCGTCCAG 2880
CCTAATTTTT TTTTTTTTTT 2900