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

TagContent
EnhancerAtlas ID
HS093-00275 
Organism
Homo sapiens 
Tissue/cell
HL-60 
Coordinate
chr1:16275990-16278530 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs848188chr116277082hg19
TF binding sites/motifs
Number: 21             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EWSR1-FLI1MA0149.1chr1:16277805-16277823GGAAGGAAGGGAGAGAGG+6.73
EWSR1-FLI1MA0149.1chr1:16277793-16277811GAGAAGAAGGAAGGAAGG+7.08
EWSR1-FLI1MA0149.1chr1:16277801-16277819GGAAGGAAGGAAGGGAGA+8.31
EWSR1-FLI1MA0149.1chr1:16277797-16277815AGAAGGAAGGAAGGAAGG+9.09
MITFMA0620.2chr1:16276939-16276957AAAGGTCACGTGAGCACA+6.13
MITFMA0620.2chr1:16276939-16276957AAAGGTCACGTGAGCACA-6.13
MSCMA0665.1chr1:16276484-16276494AACAGCTGTT+6.02
MSCMA0665.1chr1:16276484-16276494AACAGCTGTT-6.02
MYF6MA0667.1chr1:16276484-16276494AACAGCTGTT+6.02
MYF6MA0667.1chr1:16276484-16276494AACAGCTGTT-6.02
RREB1MA0073.1chr1:16277529-16277549CCACATACCACCACCCGCCA+6.33
SP1MA0079.4chr1:16276264-16276279GAAGCCACGCCCCTC+6.67
SP4MA0685.1chr1:16276264-16276281GAAGCCACGCCCCTCAC+6.35
TFAP2CMA0524.2chr1:16277366-16277378TGCCCTGGGGCT-6.11
ZNF263MA0528.1chr1:16277811-16277832AAGGGAGAGAGGGAGGGAGGG+6.03
ZNF263MA0528.1chr1:16277815-16277836GAGAGAGGGAGGGAGGGAGGG+6.11
ZNF263MA0528.1chr1:16276035-16276056TTCTCTGCCTACTCCTCCTCT-6.37
ZNF263MA0528.1chr1:16277795-16277816GAAGAAGGAAGGAAGGAAGGG+6.4
ZNF263MA0528.1chr1:16277802-16277823GAAGGAAGGAAGGGAGAGAGG+6.5
ZNF263MA0528.1chr1:16277798-16277819GAAGGAAGGAAGGAAGGGAGA+6.85
ZNF263MA0528.1chr1:16277806-16277827GAAGGAAGGGAGAGAGGGAGG+6.95
Number of super-enhancer constituents: 24             
IDCoordinateTissue/cell
SE_01097chr1:16275403-16279590Adrenal_Gland
SE_01987chr1:16272432-16279631Aorta
SE_02709chr1:16274610-16280662Astrocytes
SE_03452chr1:16275260-16277700Brain_Angular_Gyrus
SE_04408chr1:16274061-16278759Brain_Anterior_Caudate
SE_05249chr1:16273948-16279656Brain_Cingulate_Gyrus
SE_06124chr1:16270812-16279644Brain_Hippocampus_Middle
SE_07342chr1:16272948-16278751Brain_Hippocampus_Middle_150
SE_08131chr1:16272535-16279679Brain_Inferior_Temporal_Lobe
SE_18522chr1:16273733-16281386CD4p_CD25-_Il17-_PMAstim_Th
SE_19255chr1:16273419-16281362CD4p_CD25-_Il17p_PMAstim_Th17
SE_27189chr1:16274173-16281550Esophagus
SE_36664chr1:16274460-16277822HMEC
SE_36664chr1:16277848-16281222HMEC
SE_38820chr1:16274752-16281466HUVEC
SE_40080chr1:16274659-16281418K562
SE_45001chr1:16274543-16280813NHLF
SE_45986chr1:16274066-16281079Osteoblasts
SE_47059chr1:16275327-16277770Ovary
SE_47059chr1:16277811-16278793Ovary
SE_55849chr1:16274274-16283539u87
SE_61132chr1:16274043-16303645HBL1
SE_64852chr1:16274416-16281190NHEK
SE_67570chr1:16274274-16283539u87
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 3             
ChromosomeStartEnd
chr11627808216278452
chr11627602816276482
chr11627735016278224
Number: 1             
IDChromosomeStartEnd
GH01I015947chr11627401116281336
Enhancer Sequence
CACGGCTGTC ACGCCCTGGC CCAGGATCTG CTAAGGGGTA GTGAGTTCTC TGCCTACTCC 60
TCCTCTTCTC TGAGGCCTGA GTCTGCACGG GGCTGGCTCC CCGGCTTCTG GGCAGGTGAG 120
AGGGACACTT TGGGGCTCTC CGCCCCCAGT TTCGGCAGCT CTGCCCCGGC TCAGGCACTC 180
CCCTGTGACA TCAGCATCTT GGGGGGTGAA TCACTGCCGC AGCTCTGAAG CTGCTGTGGC 240
CATGCATGGC TGTCGGGCTG TGATGAGTCC GGAGGAAGCC ACGCCCCTCA CACCAGCACA 300
GGTCGGCCTT GAAGGGCGCC AAGGCCTCCC ACCACGTGAT GTCTGGAAAC TTTTCACAAG 360
TGGGGGTATC TGCTGAGCGG GGGGAAGTGA CGCAACAAAT AACGGGGAGC ATGGCAGTGG 420
CAACAGGCAT GAGCCACAGC GCACCAGCCT CCGAGCCACA AGTTCAGCGT TGCTGCTGCT 480
GCCAGAGGCC CAGAAACAGC TGTTCCCTCC CCCTACACAT CCCCGCGCAG GCTTTGGCTC 540
TCTCAATGAC ATTCCTAAAT GGCTGTGGCT AGAGCCCTAA GTGTAAGCAC TGGAGAGCCA 600
GGGCCAGCCC CGAAATCAGG AGGTAAGGCC CTGGGGCAGC TGGCCCCGCA CCAAGTGCAC 660
CAAGTGGCTG GCAGCAGCAC ACGGCCACCT GGAGCAAAGC ACAGAGGCCT TTCTCTCCTG 720
TCCTCAGTCC CTGGAAGCAG CAGGTTCCTA TCTGTGACCT GAAGGAACGC AAGGGAGAAT 780
CGTGGCTGCG CTGCTCCTAT GCACTGGACA TGGGGAGGCA CCAATGTCCA GCTTGTGGAT 840
CAAGACCTGA AGGGCACAAA GGGCAAGGTG GGTGCAGAAG GAACCAAAGG CAGGGGCGAG 900
GTGGGCCCAG GCCACGGCAA CCCTAGAGCT GTCTTCTCCT GGCTGTGGAA AAGGTCACGT 960
GAGCACACAG GTGTGTGGGT GGCAAGCCCT GGGCCTCAAT TGCTAGTCAC CCCCTACATA 1020
CCCAGGAGCC CCAAGTGCAG AAGAGGGGAA TACCAGGGCC CACACAGGGC AAAATCCTCA 1080
ACTGGCTTCA GAAGCAGCCC ATCTGGAACT TGCAAGTGAG GCCCAACCCT TCTCTCCAGG 1140
CTGTGTGCCT GGCTTCCTCA CCTTCCCCAG GAGCCAACCC GAAACTTGAG CCACCCAGGT 1200
GCTAAAACAA CCTGGGGAGC ATCAGCTGAA CCCCCAGAGG TACAAAGAAC CCTCTAGCAG 1260
GAAAACCATC TGACTTGCCG GGAAGAGACA TGTGAGGAGA CTCCTAGCCA AGGGGAGGGA 1320
CAGGATCAAT CCCCTTGTGT GGGCCCAAGG CTGGGATGAG CCTCCCTGTG GCCATGTGCC 1380
CTGGGGCTTC CTGGCAAGCG CAGCCCCGCC CAGCCATACA GCTGTCCTGG GACTGGATGG 1440
ATGGATGGAT GGGTAAGCTA GATAGATTAG ATAAGACACA TTCGCTAGAT AATAAAATAG 1500
TAAAGGCCCC AAGGACAGGG TGGGTGGTGG CCCAGCCCCC CACATACCAC CACCCGCCAA 1560
GAGAGCAGCT GTGTGCCCAT GAGCAACATT TTCCACCGTG CTGACTGCAC TTTTCCAATG 1620
CAAGATGCCC GCCCAGAAGT GGGCTCCTCC CACACACGGG TGTTAGGAGG AGAAACAGAG 1680
GCGTCTATAA TCCTCTGAGG CTGCCCCAGC AGAGAAACGC ACCAAAAGGG AAGAAAACAG 1740
GAGAAATGAT AAGAAGGGGG GAGGAAGAAG TGAAGATGGG CAAAGTAAGG GAAGGAAAGG 1800
AGAGAGAAGA AGGAAGGAAG GAAGGGAGAG AGGGAGGGAG GGAGGGGCCC TGTACCCACA 1860
GAGAGATCAG CAGCAGCTGA AATGCGCTTA CCAGTACAAT CTGGGACTGG CCTCCCAGGG 1920
GTGCAAGAGC AGCTCGAGGG GGCCAGGAGG GGGCGGACTA AGTGCTAAAT GGTGTTACCC 1980
GCAGAACTGT GTCACTGTGG ACTTTACAAC CGAAGCCCCA CCCTCACAGG GCAAGTGGAG 2040
CTCAGGGTCC CCCAGGCTGT TCCCCAGCCG GGAAGCTTTA ACAGCCCCTC TCTCAAGGCC 2100
CGTGGCGAGA CGGAGGCATG GCCGGCTGGG TCCTTCCCTC TGAGGGGCTG AGCTAGAACT 2160
AGGCAGTCCC CCACCTCCAA CCCACGTGAA CTGCTCTGGA GGGATCACCA GCCTGTATCC 2220
TAGTTCCCCT CTTATCTATT CCTCAGCGAC AGGAACCCAG CAGGACGGCC AGGCTTGGAG 2280
GGACATAGGA AAAGGGTTTG GGAGCGAAGG GGTGTGCAGG TCCTAGGAAC ATATCCCCTC 2340
CTAAGTACGT GCTAGGAGGT GCTGTCTGGG GAGACGTTAA CCACAGTAAT CAGATCAACA 2400
GCCAGCTGCT CCCCATCGCC CCCAGATGTG CGGGAACACA GGGTGAAGAA ATACTGTTCC 2460
CACCAGGCAG CCTGCCCCAC CCCACCCTTG GAATACGGTG CCCATCGCTC AAGCACAAGT 2520
GTCAAGGTCT GTGGTCTTGT 2540