EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS060-06961 
Organism
Homo sapiens 
Tissue/cell
GM12891 
Coordinate
chr11:117880430-117883440 
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
CAGACGCTTT AAAAAAAAAA AAAAAAAAAG TAGATGAGGT CTTTGCTCTC CTACAGGTAA 60
GAACCAGGAG AAGCCTTGGA AAAATAGTCC AATCTTTTGA TTCCAGATGC TGAAATAGAT 120
GTCCAAAGAG GTGGAGTAAG TAGCCCATGA CCACACAGCA CATCAGGGCA GGGTCAGAAC 180
CAGACCTTAT ACTACATTCA GTTCTCATCC TTACGCCCTG ATGTCAGCTA CATCCGTGAG 240
GGTGCAGACT CTGCTCAGCT CTGGTGCAGC CAGTAGCCAG TTGTGGAACT TGGGTAAAGC 300
ATGCTGCTTT TCTGACCCAA GTGCCCCCAT ATGTAAAACG GGACCAAGAA TAATCCCTGT 360
GTCTCAAGCT TGACATAAGG CTCAAAATGC AGTACCATGC AAGAAAAGGC TTTGTGTTCT 420
GTGGACTGTG AACTGTGCAA ACAGTCTCTG CTCCTCCTTT TGATCACTAA GCAGTTTTTA 480
AAAAGATAAT AATGATCCTC CCATCTGCTC CTACTTTGAG TTTCTCAGAC TCCTGAAGCA 540
GAGAGAGGGG CACCAGAGAC ACTGCCCTCC TGGCTCCTGG CACCTGGCCC CCTCCAATGC 600
CACTGGCATG GGACGAGATC ATTAAGACTT CAAGGAGAAC TTAGAGGAGA GAAAAGCTCC 660
CTCTTCGCCT CCCAGCCTCA TCATGATTTT GATCAATTTT CTAGGACAAA GCAGCCTTCT 720
GTGGCTACAT TGGGTGTCTC TTCTCTACTC GGCAAGTAGT CACTGACCTC CTCCAGCACG 780
CTCCAGTTTT AGGAGTTACT AAAGACCTAT GGAACATAAC TTTGTTGGCA GAGGGTTCAG 840
CCTGGTTGAG GAACAGCACA AATGGAGGAA ATGTGGCCAC CTGCAATTCA GATCAAAATG 900
GTTGGTGTCA AGTCTCAAGC CCTGAGCGAA GTCACAGCAA AGACGGACTT GGGCCATCTC 960
ACAGAGACTA GATATGGCCA GGAGGGGAGG GGCTGCAGGG ACAAGAGGCC ACCCAGGCTG 1020
GAGAATAGCC CCAGAGAAGG CACCAAAGCG TGGCAGGGGA ACCCGGACCA GCCAGCCCTT 1080
GGACCCCCAG CCCCCGTGAC TGCCTCTGGG CTCTTAGGGC CAGTGGAAAG AAGAACCGTA 1140
AAAAGGTAGC GGGAAGGTGT TGGGAGAGGC TCTGGCACTG CTATGATCTG GGTCCCAGCC 1200
AGTGCCTGGC TCAGCCAAAC CTGTGGCTGG GTTTCCAGGC ATCTGCTCCC GAATCGTTTC 1260
TAAACAAGCT GGAATCTGCC CTTTAGAGCC CTCAACAGAA ACACGCAAAG TCCAGGGGTA 1320
AGGCCCAGGC CCCAAGGGTG AAGAAAGCTG TGCTCGCCAG TAGCCTGCGG AAGTAAGGAA 1380
AAGAGGGGGA GGCTGAGGGG ACAGAGGGTG CGTCAGAGGG CCCTAAAAGA GGAAGTCGCC 1440
CAGTATCAGT TCTGCTCCCG AGGATGGGAA ATACCCTCCG TGCTCCCAGC CCCGGGCAGC 1500
TGTCCCCGTC TCCTCACCTG AAGCCACAGA CCTGGGGCCA GGGCCACCTG GGTCCTGGGT 1560
CCCATCCTCC CTTTCAAGAT TCCCCAAGGC TACTGAGTTC TGAGCACTTC CGGGGGCCTA 1620
GGGTGGCCGG GCATGGACTG CAGACCCAGG ATCCCTGCTA GGCAGGGTGC GGGTACAGAG 1680
TTTTATTGGG GCCGGGCCAG GTGCAGCAGC TGACACCTAT AATCCCAGCA CTTTGGGAGG 1740
CCGAGGCGGG TGGCTCACTT GAGGTTAGGA GTTCGGGACC AGCCTGGCCA ACATAGTGAA 1800
ACCCCATCTG TACTAAAAAT ATAAAAGTTA GTCGGGCATG ATGGCGCACA CCTGTAACCC 1860
CAGCTACTTG GGAGGCTGAG GCAGGAGGAT CCTTTGAACC TGGGAGACGG AGGTTGCAGT 1920
GAGCCAAGAT CCCGCCACTG CACTCCAGCC TGGGCAACAG GGCAAGACTC CATCTCAAAA 1980
AAAGAAAGAA AGAAAGTTTT ACTGGGGCCC AAACCTCAGG GGTTAGGAAA GAGGCCCCAG 2040
TCCTCAGAAT TGAAATCCAA GGAAGGAAGC CGAAGACAAC TCATCTCCCC TCCCTGCTAT 2100
TCCAAGAGGC CTTCAAGGAA GGGAGGGGTC TCAGAACCAC TAAGGGGCCT TCCTCACTCC 2160
CACTTACTCA GGGGCAGAAG ACTCAGTTGA AGACCTCCAA ATCCAGAGAC TTGGTAATTA 2220
AGTCAAAGCC TGGCTATGCT GGGAGAATGG CCTCCAGACC CTGGCAGAAA ATGGGGTAAG 2280
GGCTGGTGAG GCTCCCCACC TTCCTTCCTC TACAATCTGC TAGAACCCAA AACGAGAAAT 2340
GAGGCTTTGG GAAAGGGAGC ACAGGAAGAG AAATCACACA GCTTCCCTCC TCCTCCCACT 2400
TGCTCTATTG GGCTCCTGCA TCTGTTGCTG GGCTGCTAGC AGAGAGGCTG GCAGCTGGCT 2460
GTTCTAACTG CAGGTTTCAG CAGTGACAGG CTCCCTTCTC TTGCCCTACT CCATCCACAG 2520
GAGCCCCGAG GACTCTGCCT CTCTGGTTTG AACAAGTCTG CACTAAGCAC CTTCTAAGCT 2580
GACGTCCTGT GCACACTCTG CCTCCAGTCC AGCAGGGCAC AGACCGGAGA AAGGAGTGAT 2640
GACTCACGAG GGGAACTGCC CTGCTGTCTA CCAAACTACA GTGGATTCCT GGTTTCCCTG 2700
GTGCATTATC TGGTTTGTTC AGCCTCGCCT GGGTTCCTCT TCACACTCCC ACCATTTCTG 2760
GCCCACTTTT GCCACAGGAC AGGCTTTGCA CAAGAAATGC AGAACACTGT AATGTAGAAC 2820
TCACCCACTC CCCCGTGCCC AGCCCATTGC AGGAGCCTAG GCGACAAGAA CATGTTTCTA 2880
GACTGTTCTC AGCACTGCAC ATCAAAATTG GGAGTTGGCC ATGTTTGGGA GGCACTGAGG 2940
CCTTGAGCAG TAAGAGAACA GGCCCAGATT GGGGATGGGG CAGGGGGAGG GTTGAAAGTG 3000
CTGGAATCAA 3010