EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS052-21794 
Organism
Homo sapiens 
Tissue/cell
Fibroblast_foreskin 
Coordinate
chr2:178103530-178105980 
TF binding sites/motifs
Number: 6             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
IRF1MA0050.2chr2:178105846-178105867CAACAGAAAGCGAAACTGAGC-6.8
IRF9MA0653.1chr2:178105848-178105863ACAGAAAGCGAAACT+6.15
Lhx3MA0135.1chr2:178105819-178105832AAATTAATTATAC+6.19
MEF2AMA0052.3chr2:178105784-178105796TCTAAAAATAAA+6.07
Pou2f3MA0627.1chr2:178103681-178103697ATACATTTGCATACAC-6
ZfxMA0146.2chr2:178104164-178104178GAGGCCGAGGCGGG-6.01
Number of super-enhancer constituents: 35             
IDCoordinateTissue/cell
SE_04365chr2:178102487-178108824Brain_Anterior_Caudate
SE_05456chr2:178102580-178108702Brain_Cingulate_Gyrus
SE_06605chr2:178103329-178108687Brain_Hippocampus_Middle
SE_07153chr2:178102671-178108691Brain_Hippocampus_Middle_150
SE_08697chr2:178102435-178108704Brain_Inferior_Temporal_Lobe
SE_11391chr2:178102484-178108874CD20
SE_12125chr2:178104718-178106259CD3
SE_13395chr2:178103653-178108665CD34_Primary_RO01536
SE_14672chr2:178104109-178108948CD4_Memory_Primary_7pool
SE_17501chr2:178102398-178108666CD4p_CD25-_CD45RAp_Naive
SE_18040chr2:178103612-178108386CD4p_CD25-_CD45ROp_Memory
SE_20101chr2:178103064-178107859CD56
SE_24848chr2:178104749-178105506Colon_Crypt_3
SE_25905chr2:178103583-178111506Duodenum_Smooth_Muscle
SE_26714chr2:178103742-178104546Esophagus
SE_26714chr2:178104696-178105921Esophagus
SE_27757chr2:178102324-178108497Fetal_Intestine
SE_28727chr2:178102213-178108544Fetal_Intestine_Large
SE_32276chr2:178103809-178104528Gastric
SE_32276chr2:178104692-178105448Gastric
SE_35032chr2:178104215-178108759HeLa
SE_36337chr2:178104559-178108570HMEC
SE_37359chr2:178103331-178111569HSMMtube
SE_38389chr2:178104200-178111484HUVEC
SE_42450chr2:178103648-178104321Lung
SE_42450chr2:178104558-178105511Lung
SE_42450chr2:178105545-178105929Lung
SE_44916chr2:178104393-178108865NHLF
SE_45949chr2:178103517-178113015Osteoblasts
SE_49035chr2:178104655-178105372Right_Atrium
SE_50467chr2:178102571-178104331Sigmoid_Colon
SE_50467chr2:178104588-178105422Sigmoid_Colon
SE_51368chr2:178103240-178111482Skeletal_Muscle
SE_62773chr2:178104117-178132097Tonsil
SE_64314chr2:178104318-178108889NHEK
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr2178104644178105169
Number: 1             
IDChromosomeStartEnd
GH02I177237chr2178102546178111927
Enhancer Sequence
TAAAAAAGGA TTTTGATCTC AGAGATTCTG AATTATTTAC AAATAATAAA GCAAATTAAT 60
AAGCAAATTA GAAGTTTTAG TGGATATTGC TCTTGATGGT GGTTTTGTTA CTGTTGGTGG 120
GGGTAATGGT GATGGCAGTG GGCACGCCCA TATACATTTG CATACACTCT AATATAAATG 180
TTTACAAACA TACACACACA CACATTCAAT TGCCACTCAA TTCCTGCTGT GAGTACCCTT 240
CAATGGACAG CTCCAAACCA ATTCAATGTT TTTTATTTGA ATTTCCCTTG ACATGACCAG 300
AAAAAGACAT CTTTATGAAT CCTTATCAAC AAACAGGAAA AATAAGACAT GAAGCATTAT 360
TTAGACTAGC TCTTGAGCAT CCTGTTCACG TTACCTGAAA CAATGCTGGA CCCTGGGAGA 420
CTAAGCAGCT CCTGCGGCCC TAGCTTACTG TCTCCACCAA GAATGCCACC AAATGACATC 480
TAATTGCTCT TCATTAGGCT GGGGGACATT CAGTGCAATC GTAATAGGAC CAAAATAGGT 540
TTCAAAGTGT TCTGAAAGGT TTTCCTGTGT ATTTTTAAGT TTATATTTAT GTGGCCAGGC 600
ATGGTGGCTC ACGCCTATAA TCTTAGCACT TTGGGAGGCC GAGGCGGGCA GATCGCTTGT 660
GCTCAGGAGT TCGAGACCAG CCTGGGCAAC ATGGTGAAAC CCTGTCTCTA CTAAAAATAC 720
AAAAATTAGC CGGGCGTGGT GGCATGTGCC TGTAGTCCCA GCTACGTGGG GGACTAAGGT 780
GGGAGGACTG CTTGAGCCCA GGAGGTCGAG GCTGCAGTGA GCCAAGATCG TGCCACTGCA 840
CTCCAGCCTG GGTAACAAAG TGAGACCTTG TCTCAAAAAA AAGTTTATGT AATGTTTTTT 900
CTTGCTATGA GAGGTCTCAA AACAAAACAA AACAAAACTG CTTCATAAAA GAAAAAAGCT 960
AAATTTGAAG CAACTATTTT GGATTCCCAA AAACAGACAT CTTGATCAAA TTTAGAATGC 1020
AGCAACAATA GGTTTATTGT TATGGCCTTA ATGTCATACT CTGTGCTACT CAGATTTTCA 1080
CATCTGTTTC AGCAGGCAAA ATCCTGCAGA GATTTGATAC TGTATGAAAC ATTCAAAGCT 1140
TTATGTTAAA AAAAAAAAAA AAAAAACAGC AGAAGTTAAC TGAAGACTCA CTGTTGGGGA 1200
CCACAAGCTC ACTACTGTAT TTTGTGCTAA GCTAATATGC ACCAACCATT TCCTGTAAGG 1260
AGCCGTGTGA CTGGGCACAT GATTTATTCC ACAAATGACC CAGCTCTCTG CAAGGCTCAC 1320
ACATCATCTA AGAGGAAATA ATCGTCTGGG TGGAGCCCAT AACAAACAAG AACATGACAC 1380
TGGACAGGAG GAAAGGGAAG TGCCTAAGGA AGAACTAAAA CTGCTCTTCT GCACAGAAAT 1440
CCAGGGCTTT GAGGAAGTGC AAGTCCCCCA TGGAGGAAGG CCACAGTACA AAGTGTTAGA 1500
TAAGTAGGGT TTGGGTAGAG AGAGGAAAGC AGGTAGATGG GTTGCACAGC ACTGCACAGA 1560
TACTTTCTTA CAACGGGTGA GAAAGCTTCC CAAGGGCCAT GCGAGCACTG GCCAGGAGCC 1620
TTTGCATGGC ATATGGAGCA AATGCCGTCT GCCACTTGGT GTCTGAATTT TTTTTGCTCT 1680
TGTCCTTTAG TGATTCCTGA GTGTGTTCCA AATTATGTTG CTAGCTTGGC TTAGACAAAA 1740
GAAGACAATT TGATAAGAAA CACAAATGTT GGACAATTCA TGTTAAATCA CCATCTGGCC 1800
TAACAGAAAT ATTCATGTTT AAAAAATATA TATCATCATT TGCCAACTGG GTAATCTGTT 1860
ACACATTTTA GGGAAATCTG AAGTTGGACA ATTAACTCAT ACCACTTTAA AACAAACATC 1920
TTTGTACCAG GATAAACAAA GAAGAAAGGA CTTGAACACA GAATCCATAT TAAATATGTC 1980
TTTTGCAAGT CAATTTTAGT GCCTTGAATA AACCAGCATC TATCATGCTT AGATGATCCA 2040
AAATATTGGA AAAGATAAAG CAAAGATAAT ACAATCCCTG TCCTAAATTA AAGCTATTCA 2100
GTAAACTGAG ACAAAGTATT TGAAATGAAA AGTAATCTTT TAGACACTCA AATGTCTAAT 2160
TAAGGCTTGC ACCTCCCATT CCCCCGAGTC TCCCTTCCCT CTCCTACCCT CTATCTTGCC 2220
CTGAGAATGA CAGGAAGGTG GTGGGAGATT TCCTTCTAAA AATAAATTTC ATCAATAAAC 2280
TGTTAAAAAA AATTAATTAT ACACACTACT AACTCTCAAC AGAAAGCGAA ACTGAGCCTT 2340
GCTCCAAAGA GAAAACTGAT CCTTGATCTT TTTACTTTCA TGTAGTATAA AGTTGGAATG 2400
TCTTAAGTTA TTCCTTCTTA AAATCATGTA TTTCCATTTA AAAAAAATCT 2450