| Tag | Content |
|---|
EnhancerAtlas ID | HS098-30736 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr2:85671620-85674820 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr2:85672108-85672126 | GGAAGGAATCAAGGAAGA | + | 7.39 | | Myod1 | MA0499.1 | chr2:85672545-85672558 | TGCAGCTGTTGCT | + | 6.64 | | Myog | MA0500.1 | chr2:85672544-85672555 | CTGCAGCTGTT | - | 6.02 | | NR3C1 | MA0113.3 | chr2:85674710-85674727 | AAGAACATGGTGTCCTG | + | 6.05 | | Tcf12 | MA0521.1 | chr2:85672544-85672555 | CTGCAGCTGTT | - | 6.62 |
|
| | Number of super-enhancer constituents: 21 | ID | Coordinate | Tissue/cell |
| SE_01529 | chr2:85671563-85673937 | Adrenal_Gland | | SE_01529 | chr2:85673947-85675078 | Adrenal_Gland | | SE_03329 | chr2:85672780-85674917 | Brain_Angular_Gyrus | | SE_04039 | chr2:85672028-85675097 | Brain_Anterior_Caudate | | SE_05066 | chr2:85671431-85675289 | Brain_Cingulate_Gyrus | | SE_05969 | chr2:85671264-85675281 | Brain_Hippocampus_Middle | | SE_06962 | chr2:85672036-85675124 | Brain_Hippocampus_Middle_150 | | SE_08005 | chr2:85671478-85675152 | Brain_Inferior_Temporal_Lobe | | SE_08853 | chr2:85673011-85673462 | Brain_Mid_Frontal_Lobe | | SE_31856 | chr2:85672124-85673833 | Gastric | | SE_33512 | chr2:85671277-85675297 | H2171 | | SE_34480 | chr2:85671691-85674417 | HCT-116 | | SE_34718 | chr2:85671407-85674630 | HeLa | | SE_37700 | chr2:85671443-85675124 | HSMMtube | | SE_42809 | chr2:85671970-85674409 | Lung | | SE_47644 | chr2:85672270-85674916 | Pancreas | | SE_49417 | chr2:85672239-85673833 | Right_Atrium | | SE_50604 | chr2:85672193-85674477 | Sigmoid_Colon | | SE_52950 | chr2:85672321-85673793 | Small_Intestine | | SE_56638 | chr2:85672429-85674183 | u87 | | SE_65543 | chr2:85671878-85675051 | Pancreatic_islets |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr2 | 85672832 | 85673301 | | chr2 | 85673904 | 85674060 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH02I085444 | chr2 | 85671514 | 85675023 |
|
Enhancer Sequence | ACCCCAGCAC CCTCTCCCCG ATGCCCCCCA CCAGCCCTTC TACTTAGCTC CACCAGGTGT 60
GCCCTCCTAA GTGTCCTCTG GGGAGAAGTG CCCCTCCACC ATGCACTCTG GATTCCCAGG 120
AGATACAGTG GATAAAAGTC AAACATGGGT TTCAGACATT CTAATGTGGA TTTGCCCAGC 180
TTCCATGCAG CCGGGAAGTT GGAGGGACAG AAGGTGGGAG ATGAGGAGCA AAAGCACAAC 240
AGGCACCAGG GTAGGGGCTG GGTGGGGAAA GAGCATTGAA AGAGAGGGAG GTTCTGGCTG 300
AGTCATAATA GCATAGATTC CTAGGACATC TGAGCTGCTG GGCTCTGAGA CTGCCTTGTC 360
CTGTCTCCTC ACATTATAGA TGAGGAAATT AAGGCCCACG GAGGGGAGAG CAGTCTGTGA 420
ATGGAGGGGA GAGGGTAACT CCATTTTTCC TCTAGCAGCT CCTCAGCTAA GGGAAAGTCC 480
TGCCTGTGGG AAGGAATCAA GGAAGAGAGA TTGGGAAACC GAGGCCAGAG CACTAAGTTA 540
GGACTGACCA GGACAAGGGC CCCAGGCTCC CATGAGCCCG TGTTCCTGCT CCCCCGCCTG 600
CTTTCTGCTC CAGTCCCTTC TCCGGTCTCC CTTCCTTTGC CTGTAGACCT CAGCTCTGCT 660
CTCAGGACAT CCCAGATAGC AGCCCTCATG CTCAGAACAC ACTTTTCTTC CCAGGGTACA 720
TCCACTTTTG CACCCCAAGA GGATCCGGAG ATAAAGAAGG TACCAGGCAA TTCCAAACAC 780
TGGGGCTGGG TCCCAGGGAG AACAACTGAG CCAGGTGTCT CACCTGCGAA CCTCCTGTCA 840
CCTTCAGCCC TGAGATGCAA TGGCAATAAT CCATGGCCAC TTTGGAAGCC TCTCTCATAC 900
ACTGTCAGCT TGCATCTGCG GCACCTGCAG CTGTTGCTGG GGGCTCATTT TTATATTTAA 960
TTTTTTAGAG ACGAGGTTTC TCTTGCCCAG ACCAGAGTGC AGTACTGCAA TCATGACTCA 1020
CTACAGCCTT GAACTCCTGG CTCAAGCAAT CCTCCTGCCT CAGCTTCTTG AGTAGCTGAG 1080
ACTATAGGGC ACACCACCAT GTCTGGTTGT TTTTTAAATA TTTTGTAGAG ACAGAATCTC 1140
ACTATGTTGT TCAGGTGGGT CTCGAACTTC TTGGCCTCAA GCAATCCTCT TGCCTTGGCC 1200
TCCCAAAGTG TTGGGATTAC AGGCATGAGG CACTGCACCC AGCTGGAAGA TTGTTTTTAA 1260
AGCAGTGATG TCATGGCCAG AGAGAAACCA GCCCCACAGT TCCCAGATCA GCCTGGGAGA 1320
TGTCCACAAA CTTAGGAAGG CTTCCAGCAA AGAGGCCTTG GGCAGGCTGG GTGATCTCCC 1380
AGGCCCTAGG CTGTGCCTGC CCTTGATTGC ACAGAATGTT CACTGCCTGG GAAGCTGGGA 1440
GCTGGGACAG CTGGGTGACC TGGAAATGGA GGGGCTGAGG AGCTCCAGGC TGGCCTGCTC 1500
CTCCTTGCCA CCCTCTTCCT GATAACAACA GACAAGGCTG GGAGGCTCCT GGGAGCCTGC 1560
TGCCTAATTC CCAGGGCCTG GCAGCCAGCC CTGCAGCTGA TGCAAGGCCA GGGGTGGGTG 1620
AGCTCAGCCT GTCCCCAGCA CCCAGAGCCT CTTGCACCTG GTATGCCCTT GAAAATGCAT 1680
CTGTTCATGC CCCCTCTGCC TCAGCCTCCT AGGGTCCAGC TCTATTCCTT CTGAAAGCGT 1740
AGGAGGGCCA CCTAAGGATC TGGAAGCAGG CCTTGCTTGG GGGATGGGGT GGGAATTAGG 1800
CAGCAGGTTC CCAGAAGCCT CCTGGCCTTG CCTGTTGCTA TCAGGGAGAG GGTGGCAAGG 1860
AGGAACGGGG CAGCCTGGAG CTCCTCAGAC CCTCCATTTC CAGGTCATTT CTGAGCATCT 1920
CTGAGTCAAC CCCGCACCTC TGCATGGGCA GCCTAAGAGC AGTGCGGGGA CCACAGCCCC 1980
GCCTCCAGGG ACCTCTGCAG TGGAATAGAG GGGCAGGGCT CCCTGCGGGC TCTGCCCCTC 2040
AGGGTCTGTC CACACCAGCC CACTTCCTCT TCCGGGAGAG GTCAGACAGC CCCTGGGAAG 2100
TCTCCAGACC TTCTTATCCC GTGAGAAGAT GGACTTTCCT CCTCTGGCTC TCCCCTTTTA 2160
CTGGACATGC AGGCCCAATG TAGGAAGGCT GGGGCCTGTC ACTCTTCAAC AGCCCTCAGG 2220
TGTCATCAGC TCAGGACCAG GATTCATTCA GCATCTACTT ACTAAGAGCT CTGTAATGAG 2280
AATGTGACAA ATAATAACTC GACGCATATC AAATGCATGC CTCATCTTAC AAAGTGCTCT 2340
TGCGATTAGT GTTTTGAGGG ATCCTAGTGA CGATGCTGCA ACGTAGGGAG GCCCTAGGTG 2400
GAGAAACTGA GGCCCAGGGA GCTGAAGTGG CAGCACCAGG AGTCACACCA CAGGGTCTTC 2460
CCATATCCTC CTGCTACTTT AGTCCTGCCC CATACACACG CACTGAGCAG GAGGCAGGCT 2520
TCCTGCCACA TGCTCGACTG TCACAGGACA CCAGCTGGGA CAGGGAGCAG AGAACAGTGT 2580
TTCCCATGGG CAGTGGTAGA TGTAGGAGGC TGGGAGACCA GGACTTGTGG ATTTAGGGTA 2640
GTTGCATGCC AGAGCCACAG CTGTCTGGGA GGGACTGGAG ACAGGCTGAG GAGCAGGGAG 2700
GGTACCTGGA GCACTGGAGC TGTGCCTCCC TTTACCATAG CTGTTTGCTT AGACAATACT 2760
CAACTGTCCT GCTGAGCTCA GGCTGGCATC GGTAGGATTG GGTCTGTTGC CTGGGGATTG 2820
AGGCTGGCTA CAGGACCGGC TCCTCCAGTT CTGGCCAAGG ACCAGTGGCC GTGGCCATCA 2880
CTGGACTCCT CGCTGATGCC AGGATTGAAC AAGGCCTTTC CAGTCTGCCC ATTGTATCTG 2940
GGGCCTGCCC TTTGTCCTCA ACCCAGTCTG ACCGTCTCTG GGGGACCACG CACCCACCTT 3000
CATGACTCCC GGCCAACCCT CCCAGCGGCT CTTGCAGCAT ATGCAACTAC TGCTGCTGGT 3060
GAGCTCAGGC AGCTGGACTC ATGGGCAGGC AAGAACATGG TGTCCTGCGC TGGAGGGCAG 3120
GCACAGGCTG TGCCAACTGC ACCCACCTCT CCCAGACTTA GGCCTGGCAG GGAGGCCTGC 3180
AGTGTAGGCA AGGGCTCGCT 3200
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