EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS131-01918 
Organism
Homo sapiens 
Tissue/cell
ME-1 
Coordinate
chr11:117881090-117883850 
Target genes
Number: 7             
NameEnsembl ID
TF binding sites/motifs
Number: 6             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
HOXA13MA0650.2chr11:117882109-117882120GTTTTATTGGG-6.62
Myod1MA0499.1chr11:117881924-117881937GGCAGCTGTCCCC+6.29
PLAG1MA0163.1chr11:117882041-117882055GGGGGCCTAGGGTG+6.1
SPI1MA0080.4chr11:117881853-117881867TAAAAGAGGAAGTC+6.37
SPICMA0687.1chr11:117881853-117881867TAAAAGAGGAAGTC+6.75
ZfxMA0146.2chr11:117882166-117882180GAGGCCGAGGCGGG-6.01
Number of super-enhancer constituents: 23             
IDCoordinateTissue/cell
SE_09216chr11:117876042-117885309CD14
SE_10394chr11:117875274-117885085CD19_Primary
SE_11142chr11:117867323-117888043CD20
SE_12345chr11:117880705-117882001CD3
SE_12345chr11:117882336-117884056CD3
SE_14549chr11:117867915-117884191CD4_Memory_Primary_7pool
SE_18086chr11:117867365-117881943CD4p_CD25-_CD45ROp_Memory
SE_18086chr11:117882015-117883913CD4p_CD25-_CD45ROp_Memory
SE_18420chr11:117854554-117882183CD4p_CD25-_Il17-_PMAstim_Th
SE_18420chr11:117882201-117884277CD4p_CD25-_Il17-_PMAstim_Th
SE_20350chr11:117870084-117885107CD56
SE_20921chr11:117880503-117881835CD8_Memory_7pool
SE_20921chr11:117882379-117884482CD8_Memory_7pool
SE_22623chr11:117867520-117888465CD8_primiary
SE_50519chr11:117867954-117884185Sigmoid_Colon
SE_53109chr11:117875851-117881839Small_Intestine
SE_53109chr11:117882316-117883842Small_Intestine
SE_53723chr11:117876186-117884061Spleen
SE_58893chr11:117849724-117887849Ly3
SE_60148chr11:117872701-117897860Ly4
SE_60662chr11:117856089-117887742DHL6
SE_61063chr11:117855519-117924862HBL1
SE_62315chr11:117819458-117888036Tonsil
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr11117881559117881948
Number: 1             
IDChromosomeStartEnd
GH11I117997chr11117868030117885531
Enhancer Sequence
CTCTTCGCCT CCCAGCCTCA TCATGATTTT GATCAATTTT CTAGGACAAA GCAGCCTTCT 60
GTGGCTACAT TGGGTGTCTC TTCTCTACTC GGCAAGTAGT CACTGACCTC CTCCAGCACG 120
CTCCAGTTTT AGGAGTTACT AAAGACCTAT GGAACATAAC TTTGTTGGCA GAGGGTTCAG 180
CCTGGTTGAG GAACAGCACA AATGGAGGAA ATGTGGCCAC CTGCAATTCA GATCAAAATG 240
GTTGGTGTCA AGTCTCAAGC CCTGAGCGAA GTCACAGCAA AGACGGACTT GGGCCATCTC 300
ACAGAGACTA GATATGGCCA GGAGGGGAGG GGCTGCAGGG ACAAGAGGCC ACCCAGGCTG 360
GAGAATAGCC CCAGAGAAGG CACCAAAGCG TGGCAGGGGA ACCCGGACCA GCCAGCCCTT 420
GGACCCCCAG CCCCCGTGAC TGCCTCTGGG CTCTTAGGGC CAGTGGAAAG AAGAACCGTA 480
AAAAGGTAGC GGGAAGGTGT TGGGAGAGGC TCTGGCACTG CTATGATCTG GGTCCCAGCC 540
AGTGCCTGGC TCAGCCAAAC CTGTGGCTGG GTTTCCAGGC ATCTGCTCCC GAATCGTTTC 600
TAAACAAGCT GGAATCTGCC CTTTAGAGCC CTCAACAGAA ACACGCAAAG TCCAGGGGTA 660
AGGCCCAGGC CCCAAGGGTG AAGAAAGCTG TGCTCGCCAG TAGCCTGCGG AAGTAAGGAA 720
AAGAGGGGGA GGCTGAGGGG ACAGAGGGTG CGTCAGAGGG CCCTAAAAGA GGAAGTCGCC 780
CAGTATCAGT TCTGCTCCCG AGGATGGGAA ATACCCTCCG TGCTCCCAGC CCCGGGCAGC 840
TGTCCCCGTC TCCTCACCTG AAGCCACAGA CCTGGGGCCA GGGCCACCTG GGTCCTGGGT 900
CCCATCCTCC CTTTCAAGAT TCCCCAAGGC TACTGAGTTC TGAGCACTTC CGGGGGCCTA 960
GGGTGGCCGG GCATGGACTG CAGACCCAGG ATCCCTGCTA GGCAGGGTGC GGGTACAGAG 1020
TTTTATTGGG GCCGGGCCAG GTGCAGCAGC TGACACCTAT AATCCCAGCA CTTTGGGAGG 1080
CCGAGGCGGG TGGCTCACTT GAGGTTAGGA GTTCGGGACC AGCCTGGCCA ACATAGTGAA 1140
ACCCCATCTG TACTAAAAAT ATAAAAGTTA GTCGGGCATG ATGGCGCACA CCTGTAACCC 1200
CAGCTACTTG GGAGGCTGAG GCAGGAGGAT CCTTTGAACC TGGGAGACGG AGGTTGCAGT 1260
GAGCCAAGAT CCCGCCACTG CACTCCAGCC TGGGCAACAG GGCAAGACTC CATCTCAAAA 1320
AAAGAAAGAA AGAAAGTTTT ACTGGGGCCC AAACCTCAGG GGTTAGGAAA GAGGCCCCAG 1380
TCCTCAGAAT TGAAATCCAA GGAAGGAAGC CGAAGACAAC TCATCTCCCC TCCCTGCTAT 1440
TCCAAGAGGC CTTCAAGGAA GGGAGGGGTC TCAGAACCAC TAAGGGGCCT TCCTCACTCC 1500
CACTTACTCA GGGGCAGAAG ACTCAGTTGA AGACCTCCAA ATCCAGAGAC TTGGTAATTA 1560
AGTCAAAGCC TGGCTATGCT GGGAGAATGG CCTCCAGACC CTGGCAGAAA ATGGGGTAAG 1620
GGCTGGTGAG GCTCCCCACC TTCCTTCCTC TACAATCTGC TAGAACCCAA AACGAGAAAT 1680
GAGGCTTTGG GAAAGGGAGC ACAGGAAGAG AAATCACACA GCTTCCCTCC TCCTCCCACT 1740
TGCTCTATTG GGCTCCTGCA TCTGTTGCTG GGCTGCTAGC AGAGAGGCTG GCAGCTGGCT 1800
GTTCTAACTG CAGGTTTCAG CAGTGACAGG CTCCCTTCTC TTGCCCTACT CCATCCACAG 1860
GAGCCCCGAG GACTCTGCCT CTCTGGTTTG AACAAGTCTG CACTAAGCAC CTTCTAAGCT 1920
GACGTCCTGT GCACACTCTG CCTCCAGTCC AGCAGGGCAC AGACCGGAGA AAGGAGTGAT 1980
GACTCACGAG GGGAACTGCC CTGCTGTCTA CCAAACTACA GTGGATTCCT GGTTTCCCTG 2040
GTGCATTATC TGGTTTGTTC AGCCTCGCCT GGGTTCCTCT TCACACTCCC ACCATTTCTG 2100
GCCCACTTTT GCCACAGGAC AGGCTTTGCA CAAGAAATGC AGAACACTGT AATGTAGAAC 2160
TCACCCACTC CCCCGTGCCC AGCCCATTGC AGGAGCCTAG GCGACAAGAA CATGTTTCTA 2220
GACTGTTCTC AGCACTGCAC ATCAAAATTG GGAGTTGGCC ATGTTTGGGA GGCACTGAGG 2280
CCTTGAGCAG TAAGAGAACA GGCCCAGATT GGGGATGGGG CAGGGGGAGG GTTGAAAGTG 2340
CTGGAATCAA GTACAGAGGG GGCAGGGCAG AGTCGAGGCC CAGCTCAGTC TTCAGGGAAG 2400
TTGGCCTCAG GTGGGAATGT TAAAACCATG TCTGGAATCA CCTCTGTATA ACTTTGCTTA 2460
TTGAAGCTAT GAGTGGCTTT CTGGCCCCTG GTCAACCCTA CAAGGGCAGG TAACTGGAGA 2520
TACTACATAA AGAAGCTCCC TGCTGGTGTC TGGAGGCCTT GCCCACACTG GACTGCACTG 2580
GGCAGGGCTG GTTCTCCAGG ACATCTGTGA CCCCTCCTAC AGGCTCAGGG GCTTCCTGGG 2640
ATCTAGATTC CTCCTGAGGA ATGGTGGCCT CTTTTAGTTC TGAGAGAAAG CCGCTGCTGC 2700
CCAGCCAGAC TCCATTCCCA GAGGCCTGAC TCCCCAGGAC TCCCATACCA TAGGCTGGTG 2760