EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS176-07336 
Organism
Homo sapiens 
Tissue/cell
SK-N-SH 
Coordinate
chr11:62308170-62309420 
TF binding sites/motifs
Number: 3             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
Gata4MA0482.1chr11:62309229-62309240AAGAGATAAGA-6.02
JUN(var.2)MA0489.1chr11:62308890-62308904ACAAAATGACTCAT+6.03
SREBF2MA0596.1chr11:62308763-62308773ATCACCCCAT-6.02
Number of super-enhancer constituents: 49             
IDCoordinateTissue/cell
SE_00368chr11:62298188-62315779Adipose_Nuclei
SE_01094chr11:62307973-62308985Adrenal_Gland
SE_01094chr11:62309230-62315126Adrenal_Gland
SE_01800chr11:62306902-62315989Aorta
SE_02631chr11:62308133-62309021Astrocytes
SE_02952chr11:62307739-62308651Bladder
SE_09194chr11:62305125-62315417CD14
SE_10402chr11:62306931-62315152CD19_Primary
SE_11218chr11:62305482-62315422CD20
SE_11873chr11:62308074-62309239CD3
SE_14389chr11:62305417-62315771CD4_Memory_Primary_7pool
SE_16322chr11:62307747-62315182CD4_Naive_Primary_8pool
SE_16866chr11:62308347-62315442CD4p_CD225int_CD127p_Tmem
SE_17786chr11:62305015-62315682CD4p_CD25-_CD45ROp_Memory
SE_18716chr11:62305380-62314358CD4p_CD25-_Il17-_PMAstim_Th
SE_19213chr11:62305318-62315043CD4p_CD25-_Il17p_PMAstim_Th17
SE_20169chr11:62305468-62315222CD56
SE_20763chr11:62305218-62315231CD8_Memory_7pool
SE_22686chr11:62305435-62315060CD8_primiary
SE_23103chr11:62305354-62315939Colon_Crypt_1
SE_23803chr11:62308140-62309063Colon_Crypt_2
SE_24778chr11:62307767-62315199Colon_Crypt_3
SE_25890chr11:62305636-62316042Duodenum_Smooth_Muscle
SE_26647chr11:62305335-62316985Esophagus
SE_27944chr11:62309051-62315951Fetal_Intestine
SE_28960chr11:62309092-62315846Fetal_Intestine_Large
SE_29605chr11:62308133-62309298Fetal_Muscle
SE_31759chr11:62305362-62317028Gastric
SE_34339chr11:62308143-62309162HCT-116
SE_34339chr11:62309171-62316041HCT-116
SE_37400chr11:62308124-62316137HSMMtube
SE_39075chr11:62309204-62315738IMR90
SE_40680chr11:62305313-62317013Left_Ventricle
SE_41777chr11:62308189-62309056LNCaP
SE_42170chr11:62305316-62316996Lung
SE_44357chr11:62306928-62315657NHDF-Ad
SE_44871chr11:62306962-62309186NHLF
SE_47240chr11:62304772-62317371Panc1
SE_48082chr11:62305313-62316906Psoas_Muscle
SE_48636chr11:62305369-62315960Right_Atrium
SE_50083chr11:62305346-62315980Sigmoid_Colon
SE_51220chr11:62305096-62316978Skeletal_Muscle
SE_52420chr11:62305449-62315802Small_Intestine
SE_53504chr11:62305381-62315741Spleen
SE_54739chr11:62305112-62316270Stomach_Smooth_Muscle
SE_59591chr11:62306625-62315370Ly3
SE_62893chr11:62306036-62327486Tonsil
SE_64388chr11:62305450-62316346NHEK
SE_65510chr11:62307785-62308896Pancreatic_islets
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr116230820062308600
chr116230853262308826
Enhancer Sequence
GTGGAGACCC CCTAAGGCAG AAGACTGCTT GGAGGGCAGA AAAGAATGAG ATGGCGAGGC 60
CGCTCCAGCT GCAAAGGTGA GAGCACGTAT GCCTGACGCT GCGGGACAGA CTGTAATTCA 120
GGCCAGAAGC AGCAAGAGAA CAGCCCATCC TGTCACTTCA AAACTGCAAA GAGGATGTGC 180
CGAGCAGCAG GGCTCTGCCC ATACCCTGCA ACTGGGGACA ACGCCAAGTA GACGCAGAAC 240
TCCAGGAAGC AGATTCTTGA CCCCAGCAGA TGGCCTCTGC CAGGGGTGAC CTCCAGAGGA 300
GCCTCCTTCC TCCACTGCCC TCGGAGAACA GTGCCCCTTC CCCGGAGGAG CCAGTATAAA 360
GACAGCCAGG ATGGAAACCG GGCCAACTGC TGCAGCAGCT AGAGACAGCC CTGCAGCCAG 420
CGTCAGTGTG GAGATGACAG GAATTGAAAC ACACACTCCC CCAGAGACAG GCCACAGGCC 480
TCAGTGCCCA AATGCACCAA ACCTGAGGAC AAGATACACA CCACAGGGGC CCATGACTGT 540
GCATCCACCC AGCACAGGCG GGACACAGGA GGCAACCCTC CGAGGGGAAG AAAATCACCC 600
CATCCGTGGT AGGGAGGGTA CCGGCCACAG TGAAACTTCC GCCCAGCATG GCAGCACGCA 660
CATAGGCCAA TCGACCCACC ACACACACAA GGCCAAAGAG AAGCAGTCCT CATCCCAGGA 720
ACAAAATGAC TCATGCCCAG AGTTAGAGAC CCCTACCAGA GGGGAAGCCC CCAACATTCG 780
GAACCAGGAG GAGAGGGAGG CTATTCAGAG AGACACACCC AGAAGACAGT ATGGTCTGCT 840
CTCATAAACA CTCAACAGGA GGCAAAGAGG AACAGAAAGT TCCATGTTGA AAGAAAAAAA 900
AACCCCACAC ACAAGTAGAA AGAGAATTCT GCAGAGCGCT CTGATGTGCC AGGGACTGTG 960
TTGGCAACAT CCCATGCCTG GGGTCTCATT CAACTCCCAA ATGATGATGC TATGTCAAAA 1020
GAATTAATAT CCTTATTTCA GAGAAGTGAA AGCAGGCCCA AGAGATAAGA TGACTTGCCC 1080
AAGTGTGAGA CAGAGTTGAA ATGCAAGCCC AGGAGTCTCT GACCCCCAAG GCCCTTGTTC 1140
CAAAGGAACA AGGGTGACAT CCCTTCCAGG GCCTGGCCCT CTGAATGGAC CCCCGAGGAT 1200
GCAGCTGCCA GGCTTGTTTA GGAAAAAACA TTATGCCACA TTCTAACCGG 1250