EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS105-40598 
Organism
Homo sapiens 
Tissue/cell
IMR90 
Coordinate
chr19:45942370-45944080 
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: 2             
ChromosomeStartEnd
chr194594316345943490
chr194594240045942800
Number: 1             
IDChromosomeStartEnd
GH19I045439chr194594225945944857
Enhancer Sequence
GAGGTGTAGG TTGCAGTGAG CTGAGATCGC ACCACTGCAC TCCAGCCTGG GCGACAGAGC 60
GAGACTCTGT CTCAAAAAAC AAAAACAAAC AAACAAAAAA ACAAATAGCG CCTCGTTTTC 120
TGGGAGGCAG TGAATTCCCC ATTTAGGAAG TGTCCAAGCT CAAGTTGAAA TGATGGTACA 180
TTGCGGTTCA TGCTGCAATG CCTCAACCCA GTTCCTCTCC GGACCTCAGT TTCCTCATTT 240
ATAAAATGGG TGTGGACGAC GAGGTCAGAT TTAAAAAAAT AATAATAGTA GTTAATAATA 300
ATAGGCCGGG TGCAGTGGCT CAGGCCTTTA ATCCCAGCAC TTTGGGAGGC CGAGGTAGCA 360
GGATCGCTTG AGCCCAGGAG TTCTAGACAA TCCTGGGGCA ATATAGCGAG ATTCTATCTC 420
AAAGAAATAA TCATAATCAT AATAAAAATA AATGAATAGA TAAGCTGAGA CGGACTCAGG 480
CCCAGCTCCT GCCTGCGATC CCTGCGGGGG CCACCAGGGG GCGCGGCGCC CCTGCCCAAA 540
ACTCCGCCGT CGGCTCTGAA CCCCGGCGGA CGCGTCCCGA CGCCCCTGGA AGATTCTGCG 600
CCCTGCCGGC TCGCCGGCGC CCGGGAGCCC GGGAGGCGGG TGTGCACGCG GGGTGTCCAG 660
GGCGCCCCCG ATCGAGGCCC CCTCGCCGTG CCTCGGGGTA GGGGGACGGC TGTGACTCAG 720
GCGCGCGCTC CTCCCCGGGG CCCTCAGTGG TCGCGAGGGG GCGCGCACGG CCTCGGGAAC 780
CCGCGCGGCG CCGCGTCCAT TTTTACCCCA GCTCCGCTAA AAATAGTTGC CGCGCTCCGA 840
GCCGAGCCCG AAATAGCGGC CCCCAGATAA GGCAGGACGA CTCAGCGCTT CCGGGGAGCG 900
GAAGGGGGAG CGCGCGGGGG GAGCGGTGCT GGGCGCAGCC CGGCCGAGCA GGCGCCGCTG 960
TCCCCAGCGC ACCCCCACTC TGCCCTGGCG GTCACACTCG CCCCCGACTG CGACCCCGCC 1020
CCGCCGCTAG CCTGGCTGCC TTCCTACGTC CCCCACATTG TATCCTCATC CCCTGTCCCC 1080
CATCCTCAGC TTCACCTCCA TTCCTCATCA TAACTCCCCC CTCCCCTACA CCCCCAGCGA 1140
TGTCCCCCAC TGGTACTCAT CCGCATCCCC CAGCCTGTCC TACTCCTGTC CCTATTTCCC 1200
CTCTCCACCC TCATCGCCAA TCTCCTGTCG TCCTGAATCT GCCCCTTACC ATCTCTGTCC 1260
TCAAGGCCAA CCTTTATGGG GGCAGAGCAG GGCGAGAGGA TCACAGGGAG TCAGGAGACC 1320
TGCGGGCTGA GGGCTGAGGG CTGGGGGTGA GGATCTGATT TCTTGGTTTG TTTCTACTGT 1380
GGGCAGGGGT AGGCTTAGAT CTGGGGGTTG GAGCATGGGA CACTTCAGTC TGGCCTAGTC 1440
TTCAGAGCTG AGGCGAGGCA TGGCCAGCAT CACGGCTCAT TCTGTGACCA GGGTCGGGGC 1500
TCAGGCTGGG GAAGGATGAC CGTCTTTGTC ACCAAATTTG ATCACTGTGT CACCAGAGTT 1560
AGGGCTCAGC CTTGAGCCGT TTCTTTATTT ACCCACCTCC ACTAATATTT TTTATTTCAG 1620
ACAAGGCCTT GCTCTGTCGC CCAGGCTGGA GTGCAGTGTT GCCCATGCTG GAATGCAGTG 1680
CTGGGATCTT AGTTGACTGC AGCCTTGAAC 1710