EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS182-09350 
Organism
Homo sapiens 
Tissue/cell
Spleen 
Coordinate
chr17:37041110-37044350 
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: 2             
ChromosomeStartEnd
chr173704135437043177
chr173704400637044086
Number: 1             
IDChromosomeStartEnd
GH17I038876chr173703283637043967
Enhancer Sequence
TTTTTGTATT TTTAGTAGAG ACAGGGTTTT GCCACGTTGG CCAGACTGGT CTTGAACTCC 60
TGACCTCAGA TGATCCGCCC GCTTCGGCCT CCCAAAGTGC TGGCATTTCG TGCCCGACCT 120
GTATCATATA CCTTTGAAAA GTTCAGAGGG ATAGGCAGCT CCTAAGCAGG TGTGGCTGAG 180
AGGCCCCAGA ATATCTCTCA TAATGGCCGA GCTTGGAAAC GAGTTGGGTT TGAAGGATGA 240
AGTGCTTTGT TTTGCACCCA ACCTGCCAAG CACATCTTTC CCCAGAACTG AGTGCTGGAG 300
GTGGCTGGGG TCCATCTGGC CTCCCCTTCG CTGTCTGGGC AGCTGTGGTG TAGAGGAGAA 360
TGCCTTGGGC AAGGTCTCTG TCCTTGACAC TGGACCTCAG TTTCTTCATC TGTAAAACGG 420
CACAATGAGA ATGCCAGCCT AAAGCTGTGT GGTGGGTTTT GAGAGAGAAT GTGCACAGGA 480
CTCAGTGTGC CAAGATGTTG CTTTGTGTCT CTGTAAATTG TCCTGAAGCC CGAGGCTGCT 540
GCCAATAGCT GCCTGTTTGC CCTGCCCTAT CCCTGTCCAG TCCCTGTTCC TGCCCCGCTT 600
CTTCCTGTCC TACATGCCTC TCCCTGCAAA CTCCCCAGAG CAGCTGATAG CAGGGAGGAA 660
GGGTGGGTGG GGCACCTGCA GAGAGCCCAC CACCCACTTG GAATGATTAA CAAGGGGCCA 720
GTACAGGCTG GCCTATGGGA CAAAGGACAG CTGTGCTCTG GACTCTGCCC TGCACCCAGC 780
TGATCACCTG TCCCTCATTC CTCGCCATGG CCCAGTCTGT CATGGGGTTG GGTTCCAGCG 840
GAGTCACCAG CTGGGACGGG TGGCCCCTGG TCTGTCTTAG CACCCATGTT GGCATGCACA 900
CATTTCCAGC CATCCCTGCT GGGATCTAGG GGTAATGGAT GGGATGGGCA GGAAGGGAAA 960
AGGTAGAATT CCCAAAAATT GTTTCTGGAG GGAGGTCAAA TCAGTTGGAG CTTTCTTTGA 1020
AGCCCGGCAT GCTGGTGGGG GGAGGGGTGC AGCACTGATG TTCTCATGCC TTTGCTTCTA 1080
GAAACAAACC CGTGACACTT GTCCTCCTCA CCTAAATTAT CCAGAAAGAT CCTATAGACA 1140
CAGTCTCCTG ACTTTGCCCT CATGGGCTTC TCCTTAGTTG AGGACCCCCT TGCTGTCTGT 1200
GCCTCTTCCT CAACCCCCGT AGACCTCTCT CTCTCTCTCA CTCATTCTCT CTCACTCGCT 1260
CTCTCACTCT CACTCTCTCT CTCTCTCTCT CTGTCTCGCT CTCGCTCTCT CCTCACTCTC 1320
TCTCTCACTG TTGCTGCTCT CCTGCCTGGA GCTGAAGATG AGGTTGCCAT GGAAACCTGA 1380
AGCGTAGTGA GCCGGGAGAG GGAAAGGCAG AGTCGTCTCG CCAGGGCTGG GGGCTGGGGA 1440
CTGGGGACTG TGGGCTGTGG GGAGGGGACA GGGTTGACCC AGCAAGAGGA ATATAGCCCA 1500
AGCTGTCTGC CTGCCTTCCT CTGCCTGGGG TTGGGCTTAG TGGGCAGGGG AAGGAGCTTG 1560
GAGGCTCTGG AGTGCCTCTT TAATCTAGTT AATCTGATGC AGGATTAAAA TCCTCCCTCA 1620
CTCCTGCCAA ATTAAGCTGA GCTCACATCT GGGCTGGCTC ACCCCCACTT CCCTTCTGAT 1680
GGGATTAGCA CTCCAGCTGT CGGGGGCTGA GACTAGGGGG AAGGGTGCTT CTGAAGAGGA 1740
TGAAGTACCT GCCAACCCCA CCCAAGGTGC CTGCTGCATG TTGGAGGGGC TCCCGAGACC 1800
GTCTGGTGGG TGTAGGGTGA GCAGAGGGAC ACAGTGTGGG GTGCAGGGGG TGTGTGGACA 1860
TGGCCTCAAT GCAGCTGCTG CCTGGGTGTC TTGGAGGCGC CCATCGGTGC AGAGGGCACA 1920
TCTATATATT CATCGTGTGT GAGGCACAGT GCAGTGTGTG TAGGAACTTC AGACTGTGGA 1980
ATGGGTGGGG CACGTCAGGT GCACCTGTCT GGCGGTCTTT GGGCACTGGA GCTGGCCTCT 2040
GTTTTATTTA TTTATTTAAT AAAAACAGGC TCTCGCTCTG TAGCTCAGGC TGGTCTCAAA 2100
CTCCTGGCTC AAGAAATCTG CCCTCCTTGG CCTCCCAAAC TGCTGGGATT ACAGGCGTGA 2160
GCCACTGCAC CCAGCCTGGC CTGTTTTAAC CCTGTGCATT CTGGCCAATG AGAAACCCCA 2220
GGGTTTTGCA GACCGGGTCT GGAGGATGTG TTTGCCCTGC TTGCCTCTAG CCCTCCCCAT 2280
CAAATGCTAA CCAGCCTCAT CTTCTCAGAA TTGAGTCTTC GAGTGCTGGG CCAGAGCTGC 2340
CCGGAGGTCT CCTCTCCCCC ACCCTGCTTT TGCCACATGT GCCTCTACTT CCATGTGCTT 2400
GCCTCACCAC AGCCCCTGCC CATACAGTCT GCAGAATGGC TCTGATGTTG GGAGGAGGGT 2460
CGTCTCGTCT CTGAAGCGCT CCCTCTTAGG GCCTCAGGGC CTGCCAGCCC TGCTAGAGAT 2520
CTTCCCTTTC TGGTCTCTAG GAACAGACTC GTGGTTGATC ATCCCTTGGC CTGGAATTGT 2580
ACAGGAACTT TGAAGGGAGC TCCTCAGCTG TGGGTGGCCC TGGCTGCACG GGGACGACCC 2640
CAGACTTGGC CACGTATTCA TCACAGGCCA CGTCTGTTGC CAGCTGCGGA CACCTGTGTT 2700
TGCCTTTCCT CATCTTCCCT TCCTCTGCTG GAGGAACTGC GAGTCTGGGC TGACCTGGGT 2760
GGCCAGGACC CAGGTGAGGG CTGGGGGACG GGCACCGCTA GGATCATCTG GATCCGGGAC 2820
AGTGAAACTG GCCCAAGGGA AAAAGGATTT GCCAAGGTCA CCCAGTAAGT CAGTGGCAGG 2880
GCCAGAGCCC TGCACTGGGC CCTGTCAAGT TATGCTCCTT TGATTGAGGT CTCCAAATCC 2940
TGAGCCCTGC CCTTCACAAG TGGTGGCCTC AGGGGAAGTC GCCTGTTTAC AGGTAGCTCT 3000
GATGCACGGC CATGTGGGCG GCAGGAGAAC ATGCCGAGCA GAGGGGCAGC TCGTTCTTAG 3060
CTCTCGAGTG TGTCAGTTTT GGGTGGAACG TGCCTAGGAA GAGGTCCCAG GAGGCCATCT 3120
ATGGCTTACC TGGGTGCAGC CTGTGAGTCA GGGATCTGCA GGGGTCATAG CTGTGGTGGG 3180
CTGTGGTCAC CCAGGGCTAA AAATGGCCTG ACGGGCTCCG GCTTGGAGAA GCCACCCACC 3240