EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS072-00349 
Organism
Homo sapiens 
Tissue/cell
GM19193 
Coordinate
chr11:117880490-117883430 
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: 25             
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_15567chr11:117877046-117881251CD4_Memory_Primary_8pool
SE_16662chr11:117877821-117881130CD4_Naive_Primary_8pool
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
GAACCAGGAG AAGCCTTGGA AAAATAGTCC AATCTTTTGA TTCCAGATGC TGAAATAGAT 60
GTCCAAAGAG GTGGAGTAAG TAGCCCATGA CCACACAGCA CATCAGGGCA GGGTCAGAAC 120
CAGACCTTAT ACTACATTCA GTTCTCATCC TTACGCCCTG ATGTCAGCTA CATCCGTGAG 180
GGTGCAGACT CTGCTCAGCT CTGGTGCAGC CAGTAGCCAG TTGTGGAACT TGGGTAAAGC 240
ATGCTGCTTT TCTGACCCAA GTGCCCCCAT ATGTAAAACG GGACCAAGAA TAATCCCTGT 300
GTCTCAAGCT TGACATAAGG CTCAAAATGC AGTACCATGC AAGAAAAGGC TTTGTGTTCT 360
GTGGACTGTG AACTGTGCAA ACAGTCTCTG CTCCTCCTTT TGATCACTAA GCAGTTTTTA 420
AAAAGATAAT AATGATCCTC CCATCTGCTC CTACTTTGAG TTTCTCAGAC TCCTGAAGCA 480
GAGAGAGGGG CACCAGAGAC ACTGCCCTCC TGGCTCCTGG CACCTGGCCC CCTCCAATGC 540
CACTGGCATG GGACGAGATC ATTAAGACTT CAAGGAGAAC TTAGAGGAGA GAAAAGCTCC 600
CTCTTCGCCT CCCAGCCTCA TCATGATTTT GATCAATTTT CTAGGACAAA GCAGCCTTCT 660
GTGGCTACAT TGGGTGTCTC TTCTCTACTC GGCAAGTAGT CACTGACCTC CTCCAGCACG 720
CTCCAGTTTT AGGAGTTACT AAAGACCTAT GGAACATAAC TTTGTTGGCA GAGGGTTCAG 780
CCTGGTTGAG GAACAGCACA AATGGAGGAA ATGTGGCCAC CTGCAATTCA GATCAAAATG 840
GTTGGTGTCA AGTCTCAAGC CCTGAGCGAA GTCACAGCAA AGACGGACTT GGGCCATCTC 900
ACAGAGACTA GATATGGCCA GGAGGGGAGG GGCTGCAGGG ACAAGAGGCC ACCCAGGCTG 960
GAGAATAGCC CCAGAGAAGG CACCAAAGCG TGGCAGGGGA ACCCGGACCA GCCAGCCCTT 1020
GGACCCCCAG CCCCCGTGAC TGCCTCTGGG CTCTTAGGGC CAGTGGAAAG AAGAACCGTA 1080
AAAAGGTAGC GGGAAGGTGT TGGGAGAGGC TCTGGCACTG CTATGATCTG GGTCCCAGCC 1140
AGTGCCTGGC TCAGCCAAAC CTGTGGCTGG GTTTCCAGGC ATCTGCTCCC GAATCGTTTC 1200
TAAACAAGCT GGAATCTGCC CTTTAGAGCC CTCAACAGAA ACACGCAAAG TCCAGGGGTA 1260
AGGCCCAGGC CCCAAGGGTG AAGAAAGCTG TGCTCGCCAG TAGCCTGCGG AAGTAAGGAA 1320
AAGAGGGGGA GGCTGAGGGG ACAGAGGGTG CGTCAGAGGG CCCTAAAAGA GGAAGTCGCC 1380
CAGTATCAGT TCTGCTCCCG AGGATGGGAA ATACCCTCCG TGCTCCCAGC CCCGGGCAGC 1440
TGTCCCCGTC TCCTCACCTG AAGCCACAGA CCTGGGGCCA GGGCCACCTG GGTCCTGGGT 1500
CCCATCCTCC CTTTCAAGAT TCCCCAAGGC TACTGAGTTC TGAGCACTTC CGGGGGCCTA 1560
GGGTGGCCGG GCATGGACTG CAGACCCAGG ATCCCTGCTA GGCAGGGTGC GGGTACAGAG 1620
TTTTATTGGG GCCGGGCCAG GTGCAGCAGC TGACACCTAT AATCCCAGCA CTTTGGGAGG 1680
CCGAGGCGGG TGGCTCACTT GAGGTTAGGA GTTCGGGACC AGCCTGGCCA ACATAGTGAA 1740
ACCCCATCTG TACTAAAAAT ATAAAAGTTA GTCGGGCATG ATGGCGCACA CCTGTAACCC 1800
CAGCTACTTG GGAGGCTGAG GCAGGAGGAT CCTTTGAACC TGGGAGACGG AGGTTGCAGT 1860
GAGCCAAGAT CCCGCCACTG CACTCCAGCC TGGGCAACAG GGCAAGACTC CATCTCAAAA 1920
AAAGAAAGAA AGAAAGTTTT ACTGGGGCCC AAACCTCAGG GGTTAGGAAA GAGGCCCCAG 1980
TCCTCAGAAT TGAAATCCAA GGAAGGAAGC CGAAGACAAC TCATCTCCCC TCCCTGCTAT 2040
TCCAAGAGGC CTTCAAGGAA GGGAGGGGTC TCAGAACCAC TAAGGGGCCT TCCTCACTCC 2100
CACTTACTCA GGGGCAGAAG ACTCAGTTGA AGACCTCCAA ATCCAGAGAC TTGGTAATTA 2160
AGTCAAAGCC TGGCTATGCT GGGAGAATGG CCTCCAGACC CTGGCAGAAA ATGGGGTAAG 2220
GGCTGGTGAG GCTCCCCACC TTCCTTCCTC TACAATCTGC TAGAACCCAA AACGAGAAAT 2280
GAGGCTTTGG GAAAGGGAGC ACAGGAAGAG AAATCACACA GCTTCCCTCC TCCTCCCACT 2340
TGCTCTATTG GGCTCCTGCA TCTGTTGCTG GGCTGCTAGC AGAGAGGCTG GCAGCTGGCT 2400
GTTCTAACTG CAGGTTTCAG CAGTGACAGG CTCCCTTCTC TTGCCCTACT CCATCCACAG 2460
GAGCCCCGAG GACTCTGCCT CTCTGGTTTG AACAAGTCTG CACTAAGCAC CTTCTAAGCT 2520
GACGTCCTGT GCACACTCTG CCTCCAGTCC AGCAGGGCAC AGACCGGAGA AAGGAGTGAT 2580
GACTCACGAG GGGAACTGCC CTGCTGTCTA CCAAACTACA GTGGATTCCT GGTTTCCCTG 2640
GTGCATTATC TGGTTTGTTC AGCCTCGCCT GGGTTCCTCT TCACACTCCC ACCATTTCTG 2700
GCCCACTTTT GCCACAGGAC AGGCTTTGCA CAAGAAATGC AGAACACTGT AATGTAGAAC 2760
TCACCCACTC CCCCGTGCCC AGCCCATTGC AGGAGCCTAG GCGACAAGAA CATGTTTCTA 2820
GACTGTTCTC AGCACTGCAC ATCAAAATTG GGAGTTGGCC ATGTTTGGGA GGCACTGAGG 2880
CCTTGAGCAG TAAGAGAACA GGCCCAGATT GGGGATGGGG CAGGGGGAGG GTTGAAAGTG 2940