EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS098-11859 
Organism
Homo sapiens 
Tissue/cell
HSMM 
Coordinate
chr11:128480450-128483410 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs71973827chr11128482437hg19
TF binding sites/motifs
Number: 17             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EWSR1-FLI1MA0149.1chr11:128482360-128482378TCTTCCTTCCTTCCTTCC-10.05
EWSR1-FLI1MA0149.1chr11:128482348-128482366CCTCCCTTCCCTTCTTCC-7.16
EWSR1-FLI1MA0149.1chr11:128482352-128482370CCTTCCCTTCTTCCTTCC-7.71
EWSR1-FLI1MA0149.1chr11:128482356-128482374CCCTTCTTCCTTCCTTCC-8.03
EWSR1-FLI1MA0149.1chr11:128482364-128482382CCTTCCTTCCTTCCTTTC-9.6
MEF2AMA0052.3chr11:128480644-128480656TCTAAAAATAGC+6.52
MEF2AMA0052.3chr11:128482689-128482701TCTATTTATAGA-6.74
MEF2BMA0660.1chr11:128480644-128480656TCTAAAAATAGC+6.22
MEF2CMA0497.1chr11:128480642-128480657TGTCTAAAAATAGCC+6.43
SP8MA0747.1chr11:128481103-128481115AGTGGGCGTGGG-6.14
Sox6MA0515.1chr11:128482117-128482127AAAACAATGG-6.02
ZNF263MA0528.1chr11:128482289-128482310TTTTTCTTTCCTACCTCCTTC-6.03
ZNF263MA0528.1chr11:128482360-128482381TCTTCCTTCCTTCCTTCCTTT-6.24
ZNF263MA0528.1chr11:128482352-128482373CCTTCCCTTCTTCCTTCCTTC-6.29
ZNF263MA0528.1chr11:128482356-128482377CCCTTCTTCCTTCCTTCCTTC-6.55
ZNF263MA0528.1chr11:128482344-128482365CCCCCCTCCCTTCCCTTCTTC-7.2
ZNF263MA0528.1chr11:128482348-128482369CCTCCCTTCCCTTCTTCCTTC-7.61
Number of super-enhancer constituents: 15             
IDCoordinateTissue/cell
SE_10459chr11:128477490-128484068CD19_Primary
SE_11271chr11:128475395-128485372CD20
SE_12300chr11:128480174-128482087CD3
SE_20637chr11:128478742-128482482CD56
SE_31194chr11:128477952-128484748Fetal_Thymus
SE_39691chr11:128480139-128483943Jurkat
SE_43875chr11:128478040-128483676MM1S
SE_55300chr11:128480278-128482350Thymus
SE_55300chr11:128482514-128483089Thymus
SE_58351chr11:128471279-128501591Ly1
SE_60273chr11:128478305-128501435Ly4
SE_60712chr11:128473797-128501416DHL6
SE_61317chr11:128472205-128501508HBL1
SE_61546chr11:128473356-128502417Toledo
SE_62388chr11:128465164-128502820Tonsil
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr11128480883128481272
Number: 1             
IDChromosomeStartEnd
GH11I128607chr11128477572128484353
Enhancer Sequence
AGTCAACCCC TCCTCCCAGA ACTACCTCTG CAACTATCTG ATCCTCCAAA GATTCCCAGG 60
TATGTTTAAT TCATGCTGAA AATGCAAGGA AAAATAAAAT GTGATCGTCA AAATGTTCAA 120
AGCTCCCTCC AAGTCTCTCT CCCATTTTCT GTCCCTTTTG TGAGCACCAT CCCCCCAATG 180
GTAGGAAGCA TTTGTCTAAA AATAGCCCTT CTAAAAGACC CAATCTTTTC TGAGTTTCAT 240
AAAACATCTG CTGAACAGTT TCCTATAACT GTTTTTGGCC ATTAAATCAA AGCTGGCAAA 300
AACAATGTTC TGTTTCTGCC TTTAAAGCAC AGAATCGCCA TCAGGCCTTC CTCTCAGACC 360
CAGACGACAA TGGGGCCAGA AATAGCCACG GGAGGCTTTG AAACACCTAA AGGCCCGGGT 420
CCAAGCACAG AGTTACTAGT GTCTTGTTTT TCTCTCTTTT AAAGTGGCTG TTCGTCTCCC 480
AAGTACAGAA GAGAAACTTA GATAGGCCTA GCCTCCTGGG AGACGCTCTG CTCCCCCATG 540
CAAATTACCA CCTGCAGTGG TGGGGCGGTG TGGTTTGTGC AGCTCAGGGC TGGCAGAGAG 600
CAGAGACCGG TAGAAGTCTC GTCCTACGTT GGCAGGGGCA GCCACACATG TGGAGTGGGC 660
GTGGGGGTGG GCTGGCATCT GGCTGTATGG TTGCGCCTTC TCTATGTTGT GTCTATGCTG 720
TTCACTGGGC TCCTATTTGC TCAGGTGGCA CAGAACATGG GGGTTTGCAG CAACCTGTGC 780
AAGTCCAGGG GAAAACTCAC AGACACAAGG TCGAAAGATC TAGTAGGTTC TGTCCAGACT 840
GTGCTTCCCA CTAGCTGAGT GTCTTTGGCA AGACGTTTTA TCTCTCTGAC CCTGTCTGGG 900
CTGCAGGCAT CAGTGCAAAA ACTGCTGGGC CTTGTATACC GCAGGAGGAA GCCAGGGCTT 960
GGTATGATGC AGACAGAGGA ACTGCTCAGG GCCAGGCAGT CAGGCACTAA GAGCAGCTCA 1020
GTGCTGGAGG TCGGCCGAGG GGCACGCAAG TCAATGACAG TGCTGGAACT GAGACCTCTG 1080
TCCGTGTGTA CAAGACCCAG TCAGGGGCTG AAGACACATG AAACTGGATC CAGCCCCTGG 1140
AAGAAAAGAG GCTTTAGAAT GCCTGCTTTC TCTAGGATAA GACTTCAGTC TGTACAGTGA 1200
ACTTGAGGAT TAGGTCAAAA ACACCAAGGC AACCTCTTGA TGCCAAGGAG TAAGAGGCCA 1260
GCACGACAGG TGAAGGGACA CACGACTGAG AGATTCCAGA GCACAGGGAG TGTATCTGTG 1320
GTGCATATCT ATAGGTCTCA CATGGCACAT GCTTTGGGTC CCAGGACTTC ATACTGTCTT 1380
AAAATGGGTG ACGGGGACAA AGTCATCAAA CATTCAATGC CGTTGTCAGA GCTGGCTCAG 1440
AATGGAGATG AACCCACCTG TAAGCAAGGT GTGAGCAGAC GGGGATGAGA GCAGCTAAGA 1500
GTGCAAGGGT GGAAGAGGGC TGGACGCAAT GCACTGTGGC CCTCCTCCCC GGTCAGCTCT 1560
CCAGGCTTCT GTGCACTCTC TCCCAATTTG TACAGAATGG TCCTCACAGG CTTTGGTAGA 1620
AACTGGTTTC CATGTTCCAT GTCCGTCATA ATCTGTGATA GACTCATAAA ACAATGGAGG 1680
ATGGTCCCTG TAATCTGTGG ATACAGTTAG GTGGATACCA GGTCTATAAT TGCAAGAGCA 1740
AAATGAGGAG TGGGAGTGAA CATGTCCTTC TCGTTGTGGA TTTTCTCTGA ACATAGCCAA 1800
GTAATGATCA TGACAAGAGA GATGTTCACT CATTTTCTCT TTTTCTTTCC TACCTCCTTC 1860
TCTCCCTCTG TCTTTTCCTT TCATCCCTCC GTCCCCCCCC TCCCTTCCCT TCTTCCTTCC 1920
TTCCTTCCTT TCTCTATCTC ATGCCAGTTT GTATTAGTAG CACTCTGAGA AGAGTTTAAT 1980
TTAAAGAAAA AAAGATTAAT ATTTTACCCA AAACAGCAAA GCCAAAAAAC TGTTAAGGTA 2040
AAGAAAAATA TACTAACAGT GAAAAAAACC TTCACTTAAC GCTACTGCTA CCAGAAGACA 2100
TGGTGCAAAT TTGCTCAAAA AGGCATCATC TAGGAGATGC ACGCAACATC TGAGCAAAGG 2160
ATGCAAAGCC TGCCAACATT TTAGCTTGTT TGTGAAATTA TTTCTGCACA CTTGTCACTT 2220
TTTGAAGCAA AATGTGAGGT CTATTTATAG ATCTATATTT ATTTGATAGA ATAGCATTGA 2280
ATGGGCTGCT TTAGGGATTG CCTGTTGCAA ATTAACTCCG TGTGTGTGTG TGTGTGTGTG 2340
TGTGTGTGTG TGTGTGCGTG TGTGTGAACT TGGGATGCAG TAATGAATAG CTTGGGCTGT 2400
GCTCATAGCT CCTGCGTTCC CACCCCATTC AAAACCTACC CCTCACTCTT TCCTGGCAGC 2460
CACGCACAGA CTCCCAGACC AGAGCTTGGA CCTGCATAGT GCCTCAGATG AGCACAGCAT 2520
GTCAGCTACT AGTATAAGCA AAAGCTCAGC CAGGAAGAGG AAAGGAATGG GGCATCAGGT 2580
GGGCCAAAAT GCTTGCATCC AATATTGTAA CTGGGGGGAA AGTTTCACAG ATGACCATTT 2640
TAAAATGAAT TCAGTCAGTT TGCCATTTGG TTCTCATCCT GCCTATCCAG GGAGATGAAA 2700
GATCAGCCCC CAGTTTTCAA ATATTATATT GGACCATGCA ATAACAACAA AGTTGAGTAA 2760
GACTCTGGGT TTGCCCAACT TCTGGTCCCA GGCTCCTGTC CCAGCCAGCC CTCCTGCCCA 2820
GCCTCTCTAT GCTGCTGTGC TCCAGCAAGC ATAGCTGTGG CTGTGATGTG CACAAGACAC 2880
ACGTGGAGTG GTCCCTGAAC CCCAGGAAGC AGACCAAGCT TCCCTGGCAA GGGCCTGCTG 2940
CTGCTCTTGC CGTGCTGTGG 2960