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

TagContent
EnhancerAtlas ID
HS042-19249 
Organism
Homo sapiens 
Tissue/cell
Fetal_brain 
Coordinate
chr17:37040920-37043680 
TF binding sites/motifs
Number: 9             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
Nr2f6(var.2)MA0728.1chr17:37041162-37041177TGAACTCCTGACCTC-6.22
RFX1MA0509.2chr17:37042471-37042487GGTTGCCATGGAAACC+7.07
RFX1MA0509.2chr17:37042471-37042487GGTTGCCATGGAAACC-7.09
RFX2MA0600.2chr17:37042471-37042487GGTTGCCATGGAAACC-7.58
RFX2MA0600.2chr17:37042471-37042487GGTTGCCATGGAAACC+7.65
RFX5MA0510.2chr17:37042471-37042487GGTTGCCATGGAAACC-7.49
RFX5MA0510.2chr17:37042471-37042487GGTTGCCATGGAAACC+7.5
SOX10MA0442.2chr17:37041352-37041363TGCTTTGTTTT-6.02
ZNF263MA0528.1chr17:37043459-37043480TCCTCTCCCCCACCCTGCTTT-6.15
Number of super-enhancer constituents: 23             
IDCoordinateTissue/cell
SE_01869chr17:37041107-37042219Aorta
SE_04550chr17:37041217-37043246Brain_Anterior_Caudate
SE_06121chr17:37040932-37044381Brain_Hippocampus_Middle
SE_08151chr17:37040990-37043157Brain_Inferior_Temporal_Lobe
SE_19419chr17:37041258-37042819CD4p_CD25-_Il17p_PMAstim_Th17
SE_20407chr17:37041868-37043049CD56
SE_22571chr17:37041198-37043140CD8_primiary
SE_23506chr17:37041139-37044448Colon_Crypt_1
SE_24046chr17:37041309-37042184Colon_Crypt_2
SE_24046chr17:37042719-37043159Colon_Crypt_2
SE_24046chr17:37043169-37043889Colon_Crypt_2
SE_27795chr17:37039457-37044351Fetal_Intestine
SE_28678chr17:37038937-37044257Fetal_Intestine_Large
SE_31542chr17:37041115-37044397Gastric
SE_42353chr17:37041080-37044562Lung
SE_50172chr17:37041116-37044569Sigmoid_Colon
SE_52400chr17:37038709-37044606Small_Intestine
SE_53492chr17:37041098-37041748Spleen
SE_59348chr17:37019329-37056453Ly3
SE_62887chr17:37023359-37058235Tonsil
SE_65628chr17:37041277-37043501Pancreatic_islets
SE_68729chr17:37041065-37042402H9
SE_68729chr17:37043286-37044499H9
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr173704135437043177
Number: 1             
IDChromosomeStartEnd
GH17I038876chr173703283637043967
Enhancer Sequence
CGTGAGCCAC CACGTCCGGC TTTTTTTTTT TTTTTTTTTT TGAGATGGGG TCTCTCTCTG 60
TCTCCCAGGT GGAAGTGCAG AGGTGTGATC TCGGCTCACT ACAACCTCCG CTTCCCGGGT 120
TCAAGGGATT TTCCTGCCTC AGCCTCCTGG GTAGCTGGGA CTACAGGCGT GTGTCACCAC 180
GCCCGGCTAA TTTTTGTATT TTTAGTAGAG ACAGGGTTTT GCCACGTTGG CCAGACTGGT 240
CTTGAACTCC TGACCTCAGA TGATCCGCCC GCTTCGGCCT CCCAAAGTGC TGGCATTTCG 300
TGCCCGACCT GTATCATATA CCTTTGAAAA GTTCAGAGGG ATAGGCAGCT CCTAAGCAGG 360
TGTGGCTGAG AGGCCCCAGA ATATCTCTCA TAATGGCCGA GCTTGGAAAC GAGTTGGGTT 420
TGAAGGATGA AGTGCTTTGT TTTGCACCCA ACCTGCCAAG CACATCTTTC CCCAGAACTG 480
AGTGCTGGAG GTGGCTGGGG TCCATCTGGC CTCCCCTTCG CTGTCTGGGC AGCTGTGGTG 540
TAGAGGAGAA TGCCTTGGGC AAGGTCTCTG TCCTTGACAC TGGACCTCAG TTTCTTCATC 600
TGTAAAACGG CACAATGAGA ATGCCAGCCT AAAGCTGTGT GGTGGGTTTT GAGAGAGAAT 660
GTGCACAGGA CTCAGTGTGC CAAGATGTTG CTTTGTGTCT CTGTAAATTG TCCTGAAGCC 720
CGAGGCTGCT GCCAATAGCT GCCTGTTTGC CCTGCCCTAT CCCTGTCCAG TCCCTGTTCC 780
TGCCCCGCTT CTTCCTGTCC TACATGCCTC TCCCTGCAAA CTCCCCAGAG CAGCTGATAG 840
CAGGGAGGAA GGGTGGGTGG GGCACCTGCA GAGAGCCCAC CACCCACTTG GAATGATTAA 900
CAAGGGGCCA GTACAGGCTG GCCTATGGGA CAAAGGACAG CTGTGCTCTG GACTCTGCCC 960
TGCACCCAGC TGATCACCTG TCCCTCATTC CTCGCCATGG CCCAGTCTGT CATGGGGTTG 1020
GGTTCCAGCG GAGTCACCAG CTGGGACGGG TGGCCCCTGG TCTGTCTTAG CACCCATGTT 1080
GGCATGCACA CATTTCCAGC CATCCCTGCT GGGATCTAGG GGTAATGGAT GGGATGGGCA 1140
GGAAGGGAAA AGGTAGAATT CCCAAAAATT GTTTCTGGAG GGAGGTCAAA TCAGTTGGAG 1200
CTTTCTTTGA AGCCCGGCAT GCTGGTGGGG GGAGGGGTGC AGCACTGATG TTCTCATGCC 1260
TTTGCTTCTA GAAACAAACC CGTGACACTT GTCCTCCTCA CCTAAATTAT CCAGAAAGAT 1320
CCTATAGACA CAGTCTCCTG ACTTTGCCCT CATGGGCTTC TCCTTAGTTG AGGACCCCCT 1380
TGCTGTCTGT GCCTCTTCCT CAACCCCCGT AGACCTCTCT CTCTCTCTCA CTCATTCTCT 1440
CTCACTCGCT CTCTCACTCT CACTCTCTCT CTCTCTCTCT CTGTCTCGCT CTCGCTCTCT 1500
CCTCACTCTC TCTCTCACTG TTGCTGCTCT CCTGCCTGGA GCTGAAGATG AGGTTGCCAT 1560
GGAAACCTGA AGCGTAGTGA GCCGGGAGAG GGAAAGGCAG AGTCGTCTCG CCAGGGCTGG 1620
GGGCTGGGGA CTGGGGACTG TGGGCTGTGG GGAGGGGACA GGGTTGACCC AGCAAGAGGA 1680
ATATAGCCCA AGCTGTCTGC CTGCCTTCCT CTGCCTGGGG TTGGGCTTAG TGGGCAGGGG 1740
AAGGAGCTTG GAGGCTCTGG AGTGCCTCTT TAATCTAGTT AATCTGATGC AGGATTAAAA 1800
TCCTCCCTCA CTCCTGCCAA ATTAAGCTGA GCTCACATCT GGGCTGGCTC ACCCCCACTT 1860
CCCTTCTGAT GGGATTAGCA CTCCAGCTGT CGGGGGCTGA GACTAGGGGG AAGGGTGCTT 1920
CTGAAGAGGA TGAAGTACCT GCCAACCCCA CCCAAGGTGC CTGCTGCATG TTGGAGGGGC 1980
TCCCGAGACC GTCTGGTGGG TGTAGGGTGA GCAGAGGGAC ACAGTGTGGG GTGCAGGGGG 2040
TGTGTGGACA TGGCCTCAAT GCAGCTGCTG CCTGGGTGTC TTGGAGGCGC CCATCGGTGC 2100
AGAGGGCACA TCTATATATT CATCGTGTGT GAGGCACAGT GCAGTGTGTG TAGGAACTTC 2160
AGACTGTGGA ATGGGTGGGG CACGTCAGGT GCACCTGTCT GGCGGTCTTT GGGCACTGGA 2220
GCTGGCCTCT GTTTTATTTA TTTATTTAAT AAAAACAGGC TCTCGCTCTG TAGCTCAGGC 2280
TGGTCTCAAA CTCCTGGCTC AAGAAATCTG CCCTCCTTGG CCTCCCAAAC TGCTGGGATT 2340
ACAGGCGTGA GCCACTGCAC CCAGCCTGGC CTGTTTTAAC CCTGTGCATT CTGGCCAATG 2400
AGAAACCCCA GGGTTTTGCA GACCGGGTCT GGAGGATGTG TTTGCCCTGC TTGCCTCTAG 2460
CCCTCCCCAT CAAATGCTAA CCAGCCTCAT CTTCTCAGAA TTGAGTCTTC GAGTGCTGGG 2520
CCAGAGCTGC CCGGAGGTCT CCTCTCCCCC ACCCTGCTTT TGCCACATGT GCCTCTACTT 2580
CCATGTGCTT GCCTCACCAC AGCCCCTGCC CATACAGTCT GCAGAATGGC TCTGATGTTG 2640
GGAGGAGGGT CGTCTCGTCT CTGAAGCGCT CCCTCTTAGG GCCTCAGGGC CTGCCAGCCC 2700
TGCTAGAGAT CTTCCCTTTC TGGTCTCTAG GAACAGACTC GTGGTTGATC ATCCCTTGGC 2760