EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species

TagContent
EnhancerAtlas ID
HS052-19127 
Organism
Homo sapiens 
Tissue/cell
Fibroblast_foreskin 
Coordinate
chr19:45941970-45944820 
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
CTCAGCGTGA CCTCCGCCTC CCTGGGTCCA GCAATTCTCC TGCCTCAGCC TCCCAAGTAA 60
CTGGGATTAT AGGCATGCGC CACCACGCCC GGCTAATTTT GTATTTTTAG TAGAGACGGG 120
GTTTCTCCGT GTTGGTCAGG CTGGTCTCGA AATCCCGACC TCAAGTGATC CGCCCCACTC 180
GGCCTCCCGA AGTGCTGGGA TTACAGGTGT GAACCACCGC GCCCGGCCCG AAGTTATTCC 240
TCTTATCTGA CTGTAGTTTG GTATTTTTTA ACCGCATCTC TCTGTTCTTC CTCTCCCAAC 300
CCCATCTCTA CTAAAAATAC AAAATTAGCC AGCCGTTGTG GCGCATGCCT GTAATCCCAG 360
CTACTCGGGA GGCTAAGGCA GGAGAATTTC TTGCACCCAG GAGGTGTAGG TTGCAGTGAG 420
CTGAGATCGC ACCACTGCAC TCCAGCCTGG GCGACAGAGC GAGACTCTGT CTCAAAAAAC 480
AAAAACAAAC AAACAAAAAA ACAAATAGCG CCTCGTTTTC TGGGAGGCAG TGAATTCCCC 540
ATTTAGGAAG TGTCCAAGCT CAAGTTGAAA TGATGGTACA TTGCGGTTCA TGCTGCAATG 600
CCTCAACCCA GTTCCTCTCC GGACCTCAGT TTCCTCATTT ATAAAATGGG TGTGGACGAC 660
GAGGTCAGAT TTAAAAAAAT AATAATAGTA GTTAATAATA ATAGGCCGGG TGCAGTGGCT 720
CAGGCCTTTA ATCCCAGCAC TTTGGGAGGC CGAGGTAGCA GGATCGCTTG AGCCCAGGAG 780
TTCTAGACAA TCCTGGGGCA ATATAGCGAG ATTCTATCTC AAAGAAATAA TCATAATCAT 840
AATAAAAATA AATGAATAGA TAAGCTGAGA CGGACTCAGG CCCAGCTCCT GCCTGCGATC 900
CCTGCGGGGG CCACCAGGGG GCGCGGCGCC CCTGCCCAAA ACTCCGCCGT CGGCTCTGAA 960
CCCCGGCGGA CGCGTCCCGA CGCCCCTGGA AGATTCTGCG CCCTGCCGGC TCGCCGGCGC 1020
CCGGGAGCCC GGGAGGCGGG TGTGCACGCG GGGTGTCCAG GGCGCCCCCG ATCGAGGCCC 1080
CCTCGCCGTG CCTCGGGGTA GGGGGACGGC TGTGACTCAG GCGCGCGCTC CTCCCCGGGG 1140
CCCTCAGTGG TCGCGAGGGG GCGCGCACGG CCTCGGGAAC CCGCGCGGCG CCGCGTCCAT 1200
TTTTACCCCA GCTCCGCTAA AAATAGTTGC CGCGCTCCGA GCCGAGCCCG AAATAGCGGC 1260
CCCCAGATAA GGCAGGACGA CTCAGCGCTT CCGGGGAGCG GAAGGGGGAG CGCGCGGGGG 1320
GAGCGGTGCT GGGCGCAGCC CGGCCGAGCA GGCGCCGCTG TCCCCAGCGC ACCCCCACTC 1380
TGCCCTGGCG GTCACACTCG CCCCCGACTG CGACCCCGCC CCGCCGCTAG CCTGGCTGCC 1440
TTCCTACGTC CCCCACATTG TATCCTCATC CCCTGTCCCC CATCCTCAGC TTCACCTCCA 1500
TTCCTCATCA TAACTCCCCC CTCCCCTACA CCCCCAGCGA TGTCCCCCAC TGGTACTCAT 1560
CCGCATCCCC CAGCCTGTCC TACTCCTGTC CCTATTTCCC CTCTCCACCC TCATCGCCAA 1620
TCTCCTGTCG TCCTGAATCT GCCCCTTACC ATCTCTGTCC TCAAGGCCAA CCTTTATGGG 1680
GGCAGAGCAG GGCGAGAGGA TCACAGGGAG TCAGGAGACC TGCGGGCTGA GGGCTGAGGG 1740
CTGGGGGTGA GGATCTGATT TCTTGGTTTG TTTCTACTGT GGGCAGGGGT AGGCTTAGAT 1800
CTGGGGGTTG GAGCATGGGA CACTTCAGTC TGGCCTAGTC TTCAGAGCTG AGGCGAGGCA 1860
TGGCCAGCAT CACGGCTCAT TCTGTGACCA GGGTCGGGGC TCAGGCTGGG GAAGGATGAC 1920
CGTCTTTGTC ACCAAATTTG ATCACTGTGT CACCAGAGTT AGGGCTCAGC CTTGAGCCGT 1980
TTCTTTATTT ACCCACCTCC ACTAATATTT TTTATTTCAG ACAAGGCCTT GCTCTGTCGC 2040
CCAGGCTGGA GTGCAGTGTT GCCCATGCTG GAATGCAGTG CTGGGATCTT AGTTGACTGC 2100
AGCCTTGAAC TCCTGGGTTC AAGAGATCCT CCCACCTCAG CCTTCCTAGT AGCTGGGACT 2160
ACAGGTGTGC ACCAGCACAC CTGGCTAATT TTTCATTTTT TTGTAGAGAC AGAGTCTCCA 2220
TGCCTTGCCC GCCTTGTCCA GGCTGGTCTT GAGCTCCTGG CCTCAAGCTA TCCTCTGGCC 2280
TCCTCCTAGG AAGGCACTGA AATGACAGGC ATGAGCTACA GAGCCCGCCT CCACTAAGAT 2340
TCTTTCCTCC CTTGCAAGTC AGTGATTGGA CACAACAGCT CCAGGCCTTG GGAACAGTCA 2400
GAACTCTGTT CCCTGGGCCT AGGTCTTCCC TTTGCACTGA GATCATCTAA GGGCCTCCCC 2460
ATTTCCATAT CCTGAGATTC TCAGTGCCCA CTCCAAGCAT CAGTGTCAGG CCTCAAGGAC 2520
CTACACTGCA TGTTCTGGGG GTTTAAAGGG AGCACACTGA CTTCCCTGAG GGTGACAGAG 2580
GTCAGAATGA GTGACTAAGG TCTTGGGCCT GGCCCTGACC CTGCAGTGGG TGGGAGAGAT 2640
ACCCAGTTGA GGCCCAGGTC TCCACCCAGG TAGCAGGGTG GATGGCGGGG GGGTCATCCC 2700
TGAGGTGAAA TGTGGGTGGA AGATACCTAG ATAAGTTTCA GAGTCAGTGC AGAGATGGTA 2760
ATTTTTAAGT AACTTCTAAA ATTTTCGAGT AGCTGGGATT ACAGGCGCCT GCTACCAAGC 2820
CTGGCTAATT TTTGTATTTT TTTGTAGAGA 2850