EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS099-00203 
Organism
Homo sapiens 
Tissue/cell
HSMMtube 
Coordinate
chr1:10740580-10743170 
TF binding sites/motifs
Number: 5             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
ALX3MA0634.1chr1:10741659-10741669TTTAATTAGA-6.02
FOSMA0476.1chr1:10740824-10740835AATGAGTCACC-6.02
TCF7L2MA0523.1chr1:10741389-10741403AGAGATCAAAGGGC+6.25
ZNF263MA0528.1chr1:10741292-10741313CCCTCATCCCCATCCTCACCC-6.28
ZfxMA0146.2chr1:10742953-10742967TGGGCCGGGGCCTG+6
Number of super-enhancer constituents: 30             
IDCoordinateTissue/cell
SE_23439chr1:10739259-10740980Colon_Crypt_1
SE_23439chr1:10741265-10742010Colon_Crypt_1
SE_23439chr1:10742041-10743529Colon_Crypt_1
SE_24212chr1:10740357-10740976Colon_Crypt_2
SE_24212chr1:10741286-10741703Colon_Crypt_2
SE_24212chr1:10742184-10742455Colon_Crypt_2
SE_25175chr1:10739870-10741120Colon_Crypt_3
SE_25175chr1:10741188-10742076Colon_Crypt_3
SE_25175chr1:10742685-10743189Colon_Crypt_3
SE_26713chr1:10739834-10743868Esophagus
SE_28494chr1:10740371-10740988Fetal_Intestine
SE_28494chr1:10741176-10743659Fetal_Intestine
SE_30102chr1:10740351-10744027Fetal_Muscle
SE_31374chr1:10732699-10751186Gastric
SE_33519chr1:10736191-10741085H2171
SE_33519chr1:10741115-10749401H2171
SE_37889chr1:10737466-10743900HSMMtube
SE_40607chr1:10733336-10741092Left_Ventricle
SE_40607chr1:10741152-10758351Left_Ventricle
SE_41555chr1:10738952-10740970LNCaP
SE_41555chr1:10741274-10741996LNCaP
SE_41555chr1:10742068-10744836LNCaP
SE_42099chr1:10732695-10754653Lung
SE_48550chr1:10741161-10749149Psoas_Muscle
SE_48591chr1:10740346-10741076Right_Atrium
SE_48591chr1:10741162-10751093Right_Atrium
SE_54510chr1:10711383-10754578Stomach_Smooth_Muscle
SE_57180chr1:10740403-10740845VACO_400
SE_63296chr1:10733447-10756197NCI-H82
SE_65281chr1:10740888-10754570Pancreatic_islets
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr11074147210741585
Number: 1             
IDChromosomeStartEnd
GH01I010662chr11072254410750567
Enhancer Sequence
TTTGGGTCTC AGGGGGTGCA GTGTTGCACG CTCCAGCATT ACTGTGTCAC ACTCCAGAGC 60
GCAAAGGGTA GGGCAACTTT GGGCTGGAGG AGGGCGTCCA AGAGGCCACA CCCCGGCTGG 120
GCCCTGAGGT CAGCGGGTGG AGAAGGTGAA GGGGCAGGCG GGCAGACGGA CTTGCTGCTG 180
AGCCCAGCTG GGCCCTCTCC AGTTCCTCCA TGCAGGTCTG AAGCCTCCGT CCCACCCCAC 240
TACCAATGAG TCACCAGCAA CAGGGACTAG GAAGCGGGAA AGCAGACGCA GCCCCAGTCT 300
TTGGGGACAC ACACTGACTT CCCGGGTGTT CCCCCTCCCA CTGGGGCAGG GCTGGGGCCT 360
CACCCCCATC TTTCTTTCTT TCTTTCTTTT TTTTGGAGAC AGGGTCTTAC TCTGTCGCCC 420
AGGCTGGAGT GCAGTGGCAC AATCTCGGCT CACTGCAACC TCCACCTCCT GGATTCAAGC 480
GATTCTCCTG CCTCAGCCTC CCAAGTCGCT GGGATTACAG GCGCCTGCCA CCACACTTGG 540
CTACTTTTTG AATTTTTAGT AGAGACGGGG TTTCGCCATG TTGGCCCGGC TGGTTTCGAA 600
CTTCCAGCCT CAAGTGATCT GCCCGCCTTG GCCTCCCAAA GTGCTGGGAT TATAGGCAGG 660
AGCCACCGTG CCTGACCTTT TTTTTTTTTT CCTTGAAGTC TTTTATCCAT TACCCTCATC 720
CCCATCCTCA CCCTGACCTC CACGCCTGGC CCAGGTGGGT CGGGATGGTG GAAGGGTGGA 780
CAGAAGAGCA TGTACGGGGT CAGTCACTCA GAGATCAAAG GGCACAGCCC AGACCCTACT 840
CCACCTGCCA GCCAGCCCAT GTGAGGCAGC GCCCGCCTCT CCCTGCCAGG CCCTCAGCAC 900
GCTGCCCCCT CAGCGGCAGA AACTGCTCCT TCACCTCAGA GCCCGGCCAC CCCTCCTCCT 960
ACACAGCCTT CATGGGTCCC AGCTGACATT TCACTTTCTC TGGGCAGCCT CCCGGGACTG 1020
TCCTCTCCCT CTGTCCTCAC TGCACCCTGT CCTAGTCTTA GCACTTTCAT AGTAACTTGT 1080
TTAATTAGAC CTCTGCCTCA CCAGACTGCA AGATCCCTGG GACGAGACCA CTGTTTCAGC 1140
GCAGTGTCTG GCCCAACAAA TATTGACTGA GTGAATGCAG AAAACCCAGT GCTTCTGGAG 1200
CTCGTTAGGG TGGCGCTGGG CCCCAGGGAC GTGGCCTGGC TTCTGGACTG ACCCCCTCGG 1260
GGCTCCAGGA ACCTTTCCTG GAGGGGTGGG GTGGGGACTC CCTGGGTGGG ACTGAGCTGA 1320
AGCCCCTTCT CTTGGGTCTC TGGCCCTCTT GAGCCCCAGG CTCACCTCCA AACGCCCTTC 1380
ACAGGGCTCT ACCCAGAGAA CAAAAGAGGC CCCAGTTGTT CGAACATTTC TCGGCGAGAG 1440
GAACAACTGT TGCTGGCCAG TCCCTTTCTG AATAAATCCT GCAACTGTTT GCAGTGAAGT 1500
GCGACTCTCT CCCTCCACCT CCTGTCCCTG TCCCAAAAGG AGAAAAGGGG ATTGAAAAAA 1560
AGATGGGGGA AAATCCCATA CCAAGCCCCA CCATCTCCCT ACATCCACTT TCAAGTTTGT 1620
CTGAAAATGT TATAAACACA ACACACAGGG ACAGCCACCT GCTGTCCCAG ACAACTGGGA 1680
CAGCCGCAGC TAAGGGTGAG GCTGTGAGAT CAGGACCCAA AAACAGGAGG TGAGACAGTG 1740
AAGGCTGGAG GGAAGTGGGG GGTGCCGGGA CGGGGAGAAG GGGCAACGGG AAATATCACC 1800
GTGAAGTGGG AGAGGCAGAG GGCAGGGTTG TACTCAGCCC TGCAGAGGCA GAGGGAGGAG 1860
TGTCTGTGGA TCAAGGGCCC CGGAAGACTC CTGGGGGCCC GGCGGAATCC GGGAGGCAGG 1920
AGCTTCCAGT GGGGCAGTGG ATACCGAGAG GGGAAGTAGA GGAGGGAGAG AAGTTGAGTG 1980
GGGAAGAGGG AGCGAGGTCT ATTAAAAACC TCTCAGTGCA TAACACAAAA TGTCAGGGTT 2040
TATAGCTTCA TTCTTGGCTT TGCCGGGACT GAGAACCCTG AACAGAAATG TCACCGCTTG 2100
TCATGTTTAA TCACCTGCTG TTTGTTAACA CCTTCCCTGC AAGGAGCCTG TCTCAATCTG 2160
TCCCTGGGCC CCCCAGGGAC CAGGAAATAG AAAACATCTC CATCTCCTTC TCTGGGCTCT 2220
TGGCCCTGCC TAGGGGCTCT TCAGCTCCAT CTGAAGGCCT CCCGAGGAGC CCCAAAGTGA 2280
TCCTTCCTAT CAGGGAGGCC AGGGAAAGGA ACCCCATATG GCCCTTGGAG GCGTGGTGCC 2340
ATCTGTGGCC CTGCGTGGTG CGCTTGGTGT GGCTGGGCCG GGGCCTGTCA TCCCCCTGCT 2400
TCTTGTGCCT GGCTCTCCAG GCCTGCCTGT CCATTCTAGC TATTCCACTC GGTCCTCTAA 2460
CTCTGCGGGT ACGCAAAGAT AAATAAAGGA GAGCCCGCTC TGATCTCTGC AGTCTGGAAG 2520
TCACCAATCT GTCTGCTTAA ACAGCAACGG TCACATAACA TCTAACAACC AAAGCCACCA 2580
TCCTTCCAGT 2590