| Tag | Content |
|---|
EnhancerAtlas ID | HS154-05073 |
Organism | Homo sapiens |
Tissue/cell | Osteoblast |
Coordinate | chr12:58257610-58259970 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| GLI2 | MA0734.2 | chr12:58257626-58257641 | CATCGTGTGTGGCCT | - | 6.18 | | MIXL1 | MA0662.1 | chr12:58258300-58258310 | TCTAATTAAC | + | 6.02 | | YY1 | MA0095.2 | chr12:58257744-58257756 | GCAGCCATTTTG | - | 6.52 | | Zfx | MA0146.2 | chr12:58259063-58259077 | GGGGGCCCGGCCTG | + | 6.02 |
|
| | Number of super-enhancer constituents: 24 | ID | Coordinate | Tissue/cell |
| SE_01602 | chr12:58256570-58259604 | Aorta | | SE_03465 | chr12:58257834-58258487 | Brain_Angular_Gyrus | | SE_03465 | chr12:58259275-58259770 | Brain_Angular_Gyrus | | SE_04181 | chr12:58257981-58260008 | Brain_Anterior_Caudate | | SE_05429 | chr12:58257885-58259940 | Brain_Cingulate_Gyrus | | SE_06149 | chr12:58257645-58260324 | Brain_Hippocampus_Middle | | SE_07273 | chr12:58257882-58259989 | Brain_Hippocampus_Middle_150 | | SE_23544 | chr12:58258735-58259659 | Colon_Crypt_1 | | SE_24094 | chr12:58258859-58259582 | Colon_Crypt_2 | | SE_26211 | chr12:58257419-58260149 | Duodenum_Smooth_Muscle | | SE_26717 | chr12:58257432-58259746 | Esophagus | | SE_29576 | chr12:58257727-58259951 | Fetal_Muscle | | SE_31793 | chr12:58257929-58259661 | Gastric | | SE_42147 | chr12:58257909-58259832 | Lung | | SE_46841 | chr12:58257937-58258614 | Ovary | | SE_46841 | chr12:58258713-58259581 | Ovary | | SE_48108 | chr12:58257427-58260981 | Psoas_Muscle | | SE_48620 | chr12:58257506-58259733 | Right_Atrium | | SE_49678 | chr12:58258733-58259603 | Right_Ventricle | | SE_50105 | chr12:58257312-58259665 | Sigmoid_Colon | | SE_51099 | chr12:58257569-58261177 | Skeletal_Muscle | | SE_52596 | chr12:58257931-58259626 | Small_Intestine | | SE_53450 | chr12:58257930-58259691 | Spleen | | SE_65570 | chr12:58257981-58259970 | Pancreatic_islets |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH12I057863 | chr12 | 58257413 | 58259989 |
|
Enhancer Sequence | ACACATAATT TCTGCTCATC GTGTGTGGCC TTCCTCCAGT TTCCTGGGGA TGTGAAGGAG 60
GAGGGAGGGA CCTGTCAGCT GGATGGAGAC TTCTTTGCCC AAAGTTGATA GTACCACAGT 120
GGGGCTCTTC ACAGGCAGCC ATTTTGAGAC CTGTCCAGCA CAAGGTTCTA GTTTTGGGGG 180
TCCTGTCACT TAAATAAGAA AATATTGAGT GCTTGCCTTG TGCCAGTGTC TGTTTGAAGA 240
GGCAGACCAC TGTCACTTTT CTTGTATTAT CTAATTCAGT CCACACAACA ATTGCCTTTG 300
GTGGGAATTT TAATTATTCC ATTTTACAGT TGGAGAAACT AAGGTACAGA AAGATAAAGT 360
CACTTATCCT TATCAAACAA CTAGTAAGTA GTGGAGCCAC GATTTGAACC CAAGCAGACT 420
GCCTGCAGCA TCCCTGGTCG GCACCCCTGT GCACACTGCC AAATTGTCTT ATTCTAGGAA 480
TTTCCCTTCC CTGCGCCATG ACATATTAAA AACTCAGCTA GAGGTCATTT TGAGCAAGGA 540
ACCCTTCTCC ACCCTGCCTT TCCATGAGAG GGAGTTGGGA TCCCAGAGAA GAGGAATTCC 600
AGAAGAGGCA CTGCCACTTT GGCTATTTTT CCTGCATGTT CCCCAGGCAG GGAGCGCCAG 660
CTTTTGATTT GCCAGGTGTC TCTCTGTTCT TCTAATTAAC ACCAGATCCA GCCTTTAGCC 720
AGAGCCCTGC CTATAGCTGG AATCCACCAC CATGCGGCTC AGGGGCCAGT TCGCTGTGAC 780
TGCCACAGAG GACAAAGCAA GTGCTAACTC GGGGTGGAGT CTTCTGTAAT GATGCTCCCT 840
TTGCCTCATC CATAAAAAGC TCCACTCAGA TCTACCTCGT TTGTGGTGGA GGCCAGGGTG 900
GCAGAGTGTG CAGGAGAAGG CAGAATCAGG CTGAAACAGC TCCTCTTTGC CTCCCTGGAT 960
TCTTTTCCAA AATGCTGTCA GCACTGCCAG TTGGAAAATA TTTTTCTCCC TCCCTTTGTC 1020
TTCTTTCTTA TTAAGAAAAA AAAAAAAGCC ATCTGGTGTC AAATTCACTC CTGGCACATC 1080
ATAAAGGGTA GCACTAAAAA TGTCCCCGAA AAACTAAAAG CAAAACCACA GTAGTACACA 1140
TGGGATTTAA TCTCAGCATC CTAGAATTTC AGAGTTGATA GGGCCCTCTG AGATCAAACC 1200
CTTCCTGTAG ACGGGAGGAA ACTGAGGCCG GGAGGGATTA TGTTATTCTT TCAAAAATGT 1260
TTACTGAGCG CCTACTATGT TCAAGACACT CTTCAGGCGC CGCAGATGAA TCACGAACAC 1320
AACAGTGAGG CAGAAATCCC CGCCTCCTTG GAGCTTTCCG TGGGAGGTTC TTGCCTCGGC 1380
CCTCGGGCCT GCGTCTGCCG CCGTTTTTAA ACGGCCCCGA AGTTGGGAGC TCTGGCTGGG 1440
CCACCTCCGG GCTGGGGGCC CGGCCTGGGG CCGCCCCTCT TTTCCCGCCC GGAGCCGCAG 1500
TGTCCAGAGG GGCGAAGTTT GCGGCCACCG CCGGCCGTGC AGTCTCCCGC GCTTCCCCCG 1560
CCGGAGCGCC GGCCCCGCAT TCCTCCGGGT TGAGCAACAG CTTTTCCTCC GAGGGCGGCT 1620
GGCCGGGCAA GGCGGGGCCG CCAGCGCTGG GGCCCTCGCG GGGCGCGGCC CGAGTGTCCG 1680
GGGCCTCTGG CAGCGCCCCG GGTTTAAGTG GAGCGCGGCC GCCAGACCCT CCCCGGGGAG 1740
CCGAGCTCGG AGAGGGGGGC CGCAGAGCCC AGGCCCCAGC CTGCCCTTCC TGCAGCGCCG 1800
GCGGGATTGC CGAAAGACCA AGCGGGTGCC AGGCCTCACC CGACCTTGAT GTTGGCGTTA 1860
GTCCGGGTTG ACCGCCCACT CTGACGCTCT ATACAGAGAG CTCCTTTGCT TCCATTTTTA 1920
CTCCAATCCT GGAAATTCTT TGTCGATGAA AAGGGGACAG TTTATAGTGA ACTCCAAAAG 1980
AGGGGTCCTA ACCTAACCCA GCTCTTTGAA TTTAAACACT TACAATAATC ATATGTGTGT 2040
GTGTGTATGT GTGTGTATAT ATATATGTAC ACATACATCT GTGTACACAG ACGTATGTGT 2100
ATACATACAT ATATATGTAT GCATACATGT ATGTATGCAT ACATGTATGT ATGCATAGAT 2160
GTATGTGTAT ATATGTATGT ATACATATAT ACACTCACAC ACACATATAT ACATACATAT 2220
TTGAGACAGA GTCTTGTTCT GTCCCCCAGC CTGGAGTGCA GTGGCATGAT CTCGGCTCAC 2280
TGCAACCTCC GACTCCCGGG TTCAAGCAAT TCTCCCACCT TAGTCTTTGA GTAGATGGGA 2340
CTACAGGTGC GTGCCATGCC 2360
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