EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS045-00644 
Organism
Homo sapiens 
Tissue/cell
Fetal_lung 
Coordinate
chr1:16275370-16277830 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs848188chr116277082hg19
TF binding sites/motifs
Number: 19             
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
ZNF263MA0528.1chr1:16276035-16276056TTCTCTGCCTACTCCTCCTCT-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: 22             
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_38820chr1:16274752-16281466HUVEC
SE_40080chr1:16274659-16281418K562
SE_45001chr1:16274543-16280813NHLF
SE_45986chr1:16274066-16281079Osteoblasts
SE_47059chr1:16275327-16277770Ovary
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: 1             
ChromosomeStartEnd
chr11627602816276482
Number: 1             
IDChromosomeStartEnd
GH01I015947chr11627401116281336
Enhancer Sequence
TTACAAAAAG AATGCATGAC AATCTCAGAA TAAAGGACAG ATGTTTCAAT TGGACATGTT 60
GGTCTTTAAG AAAACTTTCC TATTTTCTCA TTCTCTCATG GACAGGTGAA GACAAGACGG 120
TGTTTCATCA GCCAGTGTTG CAGAACTCGG CCCCTCTCAG GCTCTGCACG TACCCCATCC 180
CCCGACAAAG CCTAGCTCTC CCTCTCTTTC TGATTCATGG GAACTACCTA GAGTTGCGGA 240
GTCTTCTGAC TCCAGAAACC TGTGTCCTGG TGGCCATCCC AGGAGAAACA ACTTTGATCC 300
TGACCCCAAG AGCTGCTGAC CTGGCCACAA CTTCTCTGTC AAGGGCCTCA CTTAATGCCT 360
GGAAATCCCA CAAGTGAAAA TGCTCAGGAA AATTCCATGG CCCAGTGCCG AGCAGTCTTG 420
AACCGCACAA GCCGTGACTA AGTAACTATC TAAAACAGCT CTCCCTCCCG CCCCAACACC 480
ACCCAGAGTG GGCGTCAACA TCAGCAATTG TCTAGGGAAA ATAAGCGGGC CCTCTTTTCT 540
AGAAAGAACC CATTTCAGAA TGTTTGAAGA GAAAAATCAA CACCCACTGT CTGGGGCCAC 600
ATTAGACAGA TTCAACTGGG CACGGCTGTC ACGCCCTGGC CCAGGATCTG CTAAGGGGTA 660
GTGAGTTCTC TGCCTACTCC TCCTCTTCTC TGAGGCCTGA GTCTGCACGG GGCTGGCTCC 720
CCGGCTTCTG GGCAGGTGAG AGGGACACTT TGGGGCTCTC CGCCCCCAGT TTCGGCAGCT 780
CTGCCCCGGC TCAGGCACTC CCCTGTGACA TCAGCATCTT GGGGGGTGAA TCACTGCCGC 840
AGCTCTGAAG CTGCTGTGGC CATGCATGGC TGTCGGGCTG TGATGAGTCC GGAGGAAGCC 900
ACGCCCCTCA CACCAGCACA GGTCGGCCTT GAAGGGCGCC AAGGCCTCCC ACCACGTGAT 960
GTCTGGAAAC TTTTCACAAG TGGGGGTATC TGCTGAGCGG GGGGAAGTGA CGCAACAAAT 1020
AACGGGGAGC ATGGCAGTGG CAACAGGCAT GAGCCACAGC GCACCAGCCT CCGAGCCACA 1080
AGTTCAGCGT TGCTGCTGCT GCCAGAGGCC CAGAAACAGC TGTTCCCTCC CCCTACACAT 1140
CCCCGCGCAG GCTTTGGCTC TCTCAATGAC ATTCCTAAAT GGCTGTGGCT AGAGCCCTAA 1200
GTGTAAGCAC TGGAGAGCCA GGGCCAGCCC CGAAATCAGG AGGTAAGGCC CTGGGGCAGC 1260
TGGCCCCGCA CCAAGTGCAC CAAGTGGCTG GCAGCAGCAC ACGGCCACCT GGAGCAAAGC 1320
ACAGAGGCCT TTCTCTCCTG TCCTCAGTCC CTGGAAGCAG CAGGTTCCTA TCTGTGACCT 1380
GAAGGAACGC AAGGGAGAAT CGTGGCTGCG CTGCTCCTAT GCACTGGACA TGGGGAGGCA 1440
CCAATGTCCA GCTTGTGGAT CAAGACCTGA AGGGCACAAA GGGCAAGGTG GGTGCAGAAG 1500
GAACCAAAGG CAGGGGCGAG GTGGGCCCAG GCCACGGCAA CCCTAGAGCT GTCTTCTCCT 1560
GGCTGTGGAA AAGGTCACGT GAGCACACAG GTGTGTGGGT GGCAAGCCCT GGGCCTCAAT 1620
TGCTAGTCAC CCCCTACATA CCCAGGAGCC CCAAGTGCAG AAGAGGGGAA TACCAGGGCC 1680
CACACAGGGC AAAATCCTCA ACTGGCTTCA GAAGCAGCCC ATCTGGAACT TGCAAGTGAG 1740
GCCCAACCCT TCTCTCCAGG CTGTGTGCCT GGCTTCCTCA CCTTCCCCAG GAGCCAACCC 1800
GAAACTTGAG CCACCCAGGT GCTAAAACAA CCTGGGGAGC ATCAGCTGAA CCCCCAGAGG 1860
TACAAAGAAC CCTCTAGCAG GAAAACCATC TGACTTGCCG GGAAGAGACA TGTGAGGAGA 1920
CTCCTAGCCA AGGGGAGGGA CAGGATCAAT CCCCTTGTGT GGGCCCAAGG CTGGGATGAG 1980
CCTCCCTGTG GCCATGTGCC CTGGGGCTTC CTGGCAAGCG CAGCCCCGCC CAGCCATACA 2040
GCTGTCCTGG GACTGGATGG ATGGATGGAT GGGTAAGCTA GATAGATTAG ATAAGACACA 2100
TTCGCTAGAT AATAAAATAG TAAAGGCCCC AAGGACAGGG TGGGTGGTGG CCCAGCCCCC 2160
CACATACCAC CACCCGCCAA GAGAGCAGCT GTGTGCCCAT GAGCAACATT TTCCACCGTG 2220
CTGACTGCAC TTTTCCAATG CAAGATGCCC GCCCAGAAGT GGGCTCCTCC CACACACGGG 2280
TGTTAGGAGG AGAAACAGAG GCGTCTATAA TCCTCTGAGG CTGCCCCAGC AGAGAAACGC 2340
ACCAAAAGGG AAGAAAACAG GAGAAATGAT AAGAAGGGGG GAGGAAGAAG TGAAGATGGG 2400
CAAAGTAAGG GAAGGAAAGG AGAGAGAAGA AGGAAGGAAG GAAGGGAGAG AGGGAGGGAG 2460