Tag | Content |
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EnhancerAtlas ID | HS044-07888 |
Organism | Homo sapiens |
Tissue/cell | Fetal_kidney |
Coordinate | chr2:238570530-238573340 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
MEF2A | MA0052.3 | chr2:238571316-238571328 | GCTATTTATAGT | - | 6.11 | MEF2B | MA0660.1 | chr2:238571316-238571328 | GCTATTTATAGT | - | 6.74 | SP8 | MA0747.1 | chr2:238571480-238571492 | GACACGCCCACC | + | 6.02 | ZNF263 | MA0528.1 | chr2:238572669-238572690 | GGAGGAGCAGGGTGAAGGGTG | + | 6.06 | ZNF263 | MA0528.1 | chr2:238572666-238572687 | GAGGGAGGAGCAGGGTGAAGG | + | 6.33 |
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| Number of super-enhancer constituents: 25 | ID | Coordinate | Tissue/cell |
SE_01566 | chr2:238568879-238571154 | Aorta | SE_01566 | chr2:238571303-238573686 | Aorta | SE_23331 | chr2:238571349-238572688 | Colon_Crypt_1 | SE_23963 | chr2:238571497-238572221 | Colon_Crypt_2 | SE_24998 | chr2:238570520-238573269 | Colon_Crypt_3 | SE_25815 | chr2:238570466-238572445 | Duodenum_Smooth_Muscle | SE_26722 | chr2:238570190-238571204 | Esophagus | SE_26722 | chr2:238571408-238572780 | Esophagus | SE_29646 | chr2:238570702-238573032 | Fetal_Muscle | SE_31908 | chr2:238568844-238571159 | Gastric | SE_31908 | chr2:238571335-238571973 | Gastric | SE_31908 | chr2:238572010-238572953 | Gastric | SE_40633 | chr2:238570413-238573764 | Left_Ventricle | SE_42111 | chr2:238568829-238571135 | Lung | SE_42111 | chr2:238571181-238573276 | Lung | SE_44921 | chr2:238570901-238572414 | NHLF | SE_45786 | chr2:238570567-238572579 | Osteoblasts | SE_48071 | chr2:238568749-238573479 | Psoas_Muscle | SE_48757 | chr2:238572029-238573322 | Right_Atrium | SE_49604 | chr2:238572197-238573233 | Right_Ventricle | SE_51094 | chr2:238569466-238573270 | Skeletal_Muscle | SE_54582 | chr2:238569703-238573611 | Stomach_Smooth_Muscle | SE_58523 | chr2:238563966-238621920 | Ly1 | SE_59868 | chr2:238570692-238624050 | Ly4 | SE_65656 | chr2:238570576-238573536 | Pancreatic_islets |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 3 | Chromosome | Start | End |
chr2 | 238571237 | 238571811 | chr2 | 238572069 | 238572172 | chr2 | 238572122 | 238572400 |
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| Number: 1 | ID | Chromosome | Start | End |
GH02I237660 | chr2 | 238568862 | 238573173 |
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Enhancer Sequence | GACAAAATGT AAAATCTGGC TGAAGACTGA GTCCTCGTGC ACCTAGCGTG ACCCATGACA 60 GCATGCAGGT GTTGGTCTGT AGGGATGCCA TAACAAAGTG CCACAAACTG GGTGACTTAA 120 AATAACAGAA CTGTATTCTC TCACAGTTCC GGAGACCGGA AGTCCAAAGT CGAGGTATTG 180 GGCCAGGTGG GTTCCTTCTG GAGGCTCTGA GGGGAAGGTG TTCCAGGCGT CTCTCCAGCT 240 TCTGGTGCTG CTGGCAGCCC TCGGCCCTCT GGCTTGTAGA CACATCACAC CAGGCTCTGC 300 CTCCGTCTCC ACGTGGCCCC CTCCCTGGGT ATTTGTGTCT CTGTGTGCAA ATTTCTGTTT 360 CCTTATAAGA AAGTCATTGA ATGAGGGCCC ACCCTAATCT AGTACGACCT CATCTTAACT 420 TGATTGTACA CGCAAAAAGC CTATGTCCAA ATAAGGCCCC ATCCACGGGT TCTGGGTGGA 480 CATGAACTTT TGGGGGATGT TACTGAACGC AGTGCAGGGT TCTTACATTC TCACCATCAC 540 GTATATGATT TTATTCTTCA GGGTGCTAAG GTGTGGTGTG TGCCATGTGC TCTTAACCCC 600 TTAGAAAAGA TAAGGACAAT TTTTTTTTCA GGTCCAATGT CTGAATGTAT TTTTTTTCTT 660 TCTCTTAGGA TTTGAAGATA TATAACAATA TGTCATAAAC TGACCTGAAA TCCTTGTTTG 720 TTCCGCAGCG AAATCCATTA ATAATCCCTA TAACTGGGAC AGTTTTATGT TCCCATTCTC 780 GGTGTGGCTA TTTATAGTGA AACCTCACTT TCCCTGTGTT GGTTAACATT AAAAACTGGA 840 ACTGCTTCTG AGGTAGGAGG CGGGACTTGA CTCCAGAGGC GGGGCTTGGA CACTGGGCCA 900 GATTGAGGAC TAGCTAAAAC AGGCCCGGTG GGGAAAGCAG TCTTCAATCA GACACGCCCA 960 CCAGCGCTAT GTCAATTTAC CGTTGCCATG ACGGCACCCA GGCATTACCG CTCCTTTCCA 1020 CGGCAATGAC CCAGTGATTA CTACCTCTTC CTTGCATAAA CCGCTCCTTA ATCTGCATGC 1080 AATTACAAGT GAGTATAAAC AGGACTGCAA AACTGCCCTG AGGTGCTGCT CTCTGCCTGC 1140 GGGGTAGCCC TGCCCTGCGG GAGCCGGCAG GGAGCTGGAA CACTGACACT TCAGTAAAGC 1200 TGTTTTCTTC TACCTATGAC TTGCCCTTGA ATTCTTTCCT GAGCAAGGCC AAGAACCCAG 1260 ATGGGCTAAG CTCCACTTTA GGGCTCGCCT GCCCTGCATC AGTTTAACTA AACTATTAGA 1320 ATTTTTAGTT TAAAAGAAAT GAGTAAGATT GTGAGCATTC TGTGAGATGC GGAGTGAAAG 1380 AAGGTGCTGT AGTCTGAACG TTTGTGTCTC CCCTAAATTC ATGTATAGAA ATCCTAACCA 1440 CCAAGCTGAC TGTATTAGGA GGTGGGAGCT TTTAGGAGGT GATTAGGGCA TGAGAGTAAA 1500 TGAGATTAGT GCCCTTATAA AACAAACCCG GGGAGTTCTT TCCCCCCCCA TCCCGCCATG 1560 TGAGGACACA ATGGGAAGGG GGCCCTCACC CCTTCTATGA ACAAGAAAGG GGGCCCTCCC 1620 CAGACACTGA ATCTGCTGGC ACCTTGATCT TGGGCTTCAC AGCCTCTGGA ACTGGGGGAA 1680 GTTAATTTCT GTTGTTTATA AGCCACCTAG TCTATGCCCT TCTGCTACAG CAGCCTAAAC 1740 AGCTCAGCCT TAATGGACGA GGCACATGGA ATGACTTCCG GGCCTCTGAC AGGGTGCTTG 1800 GGGAGGATGG TGTGATGTTG CGTTATCACT CACAGACACT GTGGAACTGA CTGGGTTGGT 1860 GGAGCGGGGA CCCGGGGAAG AGTTCAGTTC TGTTCTGGGA ATGTTGCCTT GAGGCAGCTG 1920 AGCACTACCC ACAGGGAAAG GTCTGGCAAA GGTTCACGTG CATTCGCCTG GGCCATAGGG 1980 GAGAGGGGAG CCGTCAGCGG TCAGGGTGGT CAAAGCCACA TAGTTGCATG AGGTCTCCTA 2040 AGTAGGTCAG TGGAGCAGAG TACCCAGGGT GGAGCCCCGG GAACCTCAGA AACAAGGAAG 2100 GGGTGAGCAG AGGAAGGGTC GCCCTCAGGG CACTGGGAGG GAGGAGCAGG GTGAAGGGTG 2160 GGGGCAGAGG GGAAACAGCC ATGTCCATGC TGCAGAGAGA CCCAAGGGAG ACCCGGGGAA 2220 GAATGTCACT TGCACCTTGC AAAAGGGAGG GTCCTGGCGG CCTCAGCCAG AGCCGTTTTA 2280 GTGAAGTCAT GGGGAGAAGG ACCACAGAGG CTTAGTCCTG GCTGGGGCCG CAGTGGGACT 2340 GGCAGTGGAG AGGAGGGGGC CCAAGCCAGG GAGATTGAGT TCTTGGCAAA GAGGCCGGCG 2400 GCGTTCTCCA CTGCGTTTCC ATCCGCAGGT GCGCCTGCCG CCTGGCCTGT CCACAGTGTG 2460 CTGGTTGCTG GTATTCAGTT CTGGATTGTA CCTCTGACTG GACTGAGGTC CATCAGCAAA 2520 TGACGGGGCC TCGGCGGTGT GGCAGTGTGT TCAGCTGCTG GCATGCCGCC TCGGGAACAG 2580 AAAAGTCACG TTGTTGTGTA TGCGGGTAAC AGCTCCAGGG AGGCGTGAAG AGAACTTCCT 2640 GGCAAGGAGT GCTGCTCCAA GACTGAATGG ACTTTTTTTG AAGTGCAAGG GTCTGGCCTC 2700 TGGAAGGGTG TTTTTGCTGC CACCTTTGAA CTTCTCTGTG AGTTTTTAAA TTTTGAGCAA 2760 ATCGCCTTTT ATAATCATTC TATATGTACT TTTTCTACCC AACGGCTGCA 2810
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