EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS053-03581 
Organism
Homo sapiens 
Tissue/cell
Foreskin_keratinocyte 
Coordinate
chr1:208004760-208007280 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs859711chr1208004898hg19
TF binding sites/motifs
Number: 5             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EWSR1-FLI1MA0149.1chr1:208006828-208006846GGAAGGAAGACAGGAGGA+6.37
NFKB1MA0105.4chr1:208005402-208005415AGGGGATTCCCCA-6.71
NFKB1MA0105.4chr1:208005402-208005415AGGGGATTCCCCA+6.82
RARA(var.2)MA0730.1chr1:208005268-208005285TGACCTCTGTGTGACCA-6.3
ZNF263MA0528.1chr1:208006825-208006846AGAGGAAGGAAGACAGGAGGA+6.1
Number of super-enhancer constituents: 31             
IDCoordinateTissue/cell
SE_01610chr1:208003718-208006602Aorta
SE_01610chr1:208006681-208007933Aorta
SE_02940chr1:208003945-208006074Bladder
SE_03907chr1:208003545-208007521Brain_Anterior_Caudate
SE_06993chr1:208003570-208005482Brain_Hippocampus_Middle_150
SE_08580chr1:207991706-208006704Brain_Inferior_Temporal_Lobe
SE_09440chr1:208003916-208007804CD14
SE_10475chr1:208004630-208006320CD19_Primary
SE_11488chr1:207992533-208010277CD20
SE_12401chr1:208004637-208006256CD3
SE_13353chr1:208004754-208006344CD34_Primary_RO01536
SE_14644chr1:208004273-208007930CD4_Memory_Primary_7pool
SE_17929chr1:208003706-208007813CD4p_CD25-_CD45ROp_Memory
SE_18828chr1:207994794-208013240CD4p_CD25-_Il17-_PMAstim_Th
SE_20606chr1:208004352-208006469CD56
SE_24155chr1:208004812-208005329Colon_Crypt_2
SE_25829chr1:208003915-208006434Duodenum_Smooth_Muscle
SE_26666chr1:208003798-208005871Esophagus
SE_42138chr1:208003616-208008639Lung
SE_48593chr1:208003701-208006541Right_Atrium
SE_48593chr1:208006718-208012761Right_Atrium
SE_49524chr1:208003918-208005343Right_Ventricle
SE_50299chr1:208003929-208006142Sigmoid_Colon
SE_52485chr1:208003912-208006536Small_Intestine
SE_53314chr1:208003646-208008432Spleen
SE_54764chr1:207991828-208013085Stomach_Smooth_Muscle
SE_59011chr1:207980241-208007571Ly3
SE_61319chr1:207994376-208006461HBL1
SE_62794chr1:207980098-208006634Tonsil
SE_65312chr1:208004839-208005692Pancreatic_islets
SE_65312chr1:208005804-208008071Pancreatic_islets
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr1208006714208007152
Number: 1             
IDChromosomeStartEnd
GH01I207830chr1208003920208007544
Enhancer Sequence
GCCGCTAATC ATTAAATCTA AGCTCCCACC CCAGAGGGCT CACAACTCAG CCATAAGCAA 60
AACCCAGACT GGCAATAGCA CTGGCACCTG CTATCCTGAC TATGGGCTGG GGCTGAGTGA 120
ATGTGGCCAC TCTGCTAACC ACTGGTCACA GCTCCTGCTG CCTAAAATAC AGGAGGACAA 180
AGTCTTCTTG GGACTGAGGG AGTAACCCAA TGTGCCTCTT GGCTGGCTGC TCAAAATCTT 240
GGCCCTGCCA ATGGATGGAA ATAATTTCCA GAGAGACAGA GTGTGGTTGG GCCATGTGAG 300
AGGGACTTGA GGAGAACATT ACTCCATTCC TCAACAGCGG AACCTGTAGC CTGTGCCAGG 360
CCAGACATGG CCGGGATTGA GGGGTCTTGG CCAGACTCCC TCCAGGCACA GGTTGGTGCC 420
CTCAGACGCT GCTGCTGCTC TTGTGGGCAG GAGGAGATGT CTCTAGGGTA GGAAGAACCT 480
AGGCCTCTGA TGATTTATGG GTCTGTGCTG ACCTCTGTGT GACCACATGG GTTTAGCACC 540
ATGTGACTTA AAAATGGAGT CGCTTTCCTG CCTCACAACA AACTTCTGCT CTACTTAACT 600
GAGTCAGATC TAGACAGCAG GAATCATAAA CACAAGTGGG GCAGGGGATT CCCCAAACAC 660
TTCTGACTTG AACTTTCATT TCCATACTGC CTTATCCCCC AAGCAGGGGC ACGTCCGTAC 720
CTGCAGCCTA GGACAGAGGA GAAAAGAGAC CAGGGCCATT ATGCATGGCC TGGGTGCAGG 780
TCCGAGCTTT CAGCAAAGTG CCAGCTTTGC CAGGAGCAGG GACAAAACTT CCAGGGCCGA 840
GACTCTCATT CAGGGGTGGG AGAGGAGCTG GGGACTGTCT AAAACATAAC AGTTAATATT 900
TGGGATACGT TTTCATAATG TGAAACCATA CCAAAAGTAA AGTTCCACAA AACCTTTGAT 960
GATGTGAATA CTTCCTCTGC ACTGGGAGGG GATGTTGACC AGAATCTTTG GGGGTGGGAG 1020
GCAGTCCTGT GGTTGATTTA TTTACTGAAG GTAGGTGTTG GAATTACACT CTTTTAGAGG 1080
GTTCAGCTCT CTGAAACCCC CTGGGACCAC TGGACAGCCA TTATTCTCAG GCTAGGATTT 1140
GACATAGGCC TCCGAGGCCA ATGTTCTTTC TCCAAAAGCA GCACAGCAAC AACAGCTCTG 1200
CCTTAAAAGA CAGAAGATTA CACTTAGAAG ATTTCTCCAA CGCCACATAC TTTGGAGGTG 1260
AGAGGAGTAC CCCATCACTC TCCCTCTGAA AACTTCAAAA CCTTCAGAGG CCAGGGTGAA 1320
TATTTAGAAA GCAGGCGGGT CCAACAGAAA GAACGGCCAT TGATCTATTC CAAAAAAATA 1380
ATGTGTTTGG GGCCCATGTG TCAGGTACAG CGCGAGGCAC TTTTTAAGGA GCTCCACCCT 1440
TGGCTGGCAG GAACTCCCTC GGTCAGCAGA GGCTGGTAAA CTAAGAAAGC AAGATGCTAG 1500
GAGGACAGCT GGCTCCTTAA TCCCACCCTG GCCCCCCAAA CAAGACAGCT CAAGTCTTGC 1560
CGGCCCTGGA GGCCCAGGCA CTTGGACATC ACTTGCTCTA TGCCTTTCTT GGGAGGCAGA 1620
GCTTAGTGGG GGTTGAGGAG AGATCTACAG GCTGAGTGCG CTCATGACAC AATCAAGAAG 1680
TTTCTGGGGC CAGGTGCGGT GGCTCACGCC TGTAATTCCA GCACTTTGGG AGGCCAAAAG 1740
AAGCCAAGGC GGGCAAATCA CTTGAGGCCA GGAGTTTAAG ACCAGCCTGG CTGACATGGT 1800
GAAACCCCAT CTCTACTAAA ATTACAAAAG TTATCTGAGC ATGGTGGCAC ATGCCTGTAA 1860
TCCCAGCTAC TTGGGAGGTT GAGTCATGAG AATCGCTTGA GCCTGGGAGG TGGAGGTTGC 1920
AGTGAGCCAA GATTGTGCCA TTGTACTCCA GCCTGGGTAA CAGAGCGAGA CTCTGTCTCA 1980
AAAAATATAT ATATAAGTTT CTGGGTAGGC TGACATGAAA AAATTACCAC TGGAGCTTCT 2040
GAGAGCCCTA AATCACCATA AGGGTAGAGG AAGGAAGACA GGAGGAACTG AGATGCTGAG 2100
ATAAGCTGGG ATGTCCCAGC CCACTTCCCT AGAGAGGCCC TTTCCTAACA GCCAGCGGGA 2160
GAACCCTGTT CACGGAGCCC TATCACTGAC CTCGAGGGCA GCACCAGCAT CCACAGTCAG 2220
GTCATCCCGA GAGTCGTAAC CACTGTTCCT GCCCCAAACC CAATGACCCT CTCAACCCCA 2280
TCCAAATAGC CCAGGATGAG CCACAAGACA GGGCCTTAGA ACCCTGGGGG TGTAAGACAC 2340
CCTGAATGTC ATCTGGCCTC ACCTTCCACT GAGACAAGAA GATTCCGCCT TGGGTTAGAG 2400
TCCAAGGTGT GGGATCTTGG GTGAGTTATT CCATGTCTTG CCTAAATTCT CTCATCTATA 2460
AAGTAGGGCT GATAAGCTCA TCATACCTCT TCACAGTGTT GCTGTGAAGA TTAGAGTCTA 2520