Tag | Content |
---|
EnhancerAtlas ID | HS135-02356 |
Organism | Homo sapiens |
Tissue/cell | MM1S |
Coordinate | chr9:93953600-93956650 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
MEF2A | MA0052.3 | chr9:93955577-93955589 | GCTATTTTTAGC | - | 6.44 | MEF2A | MA0052.3 | chr9:93955890-93955902 | TCTATTTTTAGC | - | 6.92 | MEF2A | MA0052.3 | chr9:93954859-93954871 | TCTATTTTTAGA | - | 7.22 | MEF2B | MA0660.1 | chr9:93955890-93955902 | TCTATTTTTAGC | - | 6.44 | MEF2B | MA0660.1 | chr9:93955577-93955589 | GCTATTTTTAGC | - | 6.92 | MEF2C | MA0497.1 | chr9:93954858-93954873 | GTCTATTTTTAGATC | - | 6.9 | Mafb | MA0117.2 | chr9:93954777-93954789 | AAATTGCTGACA | + | 6.37 | NR2C2 | MA0504.1 | chr9:93956220-93956235 | AGGGGTCAGAAGTCA | + | 6.18 | TBP | MA0108.2 | chr9:93955273-93955288 | CTATAAAAAGGCCCC | + | 6.22 |
|
| Number of super-enhancer constituents: 19 | ID | Coordinate | Tissue/cell |
SE_24346 | chr9:93954308-93954719 | Colon_Crypt_2 | SE_24346 | chr9:93955224-93956980 | Colon_Crypt_2 | SE_25080 | chr9:93954487-93958229 | Colon_Crypt_3 | SE_26319 | chr9:93953887-93962638 | Duodenum_Smooth_Muscle | SE_27567 | chr9:93953700-93957026 | Esophagus | SE_28201 | chr9:93953588-93961571 | Fetal_Intestine | SE_29279 | chr9:93953698-93962183 | Fetal_Intestine_Large | SE_32161 | chr9:93953837-93959264 | Gastric | SE_35319 | chr9:93953586-93962988 | HepG2 | SE_39461 | chr9:93953161-93957016 | Jurkat | SE_44449 | chr9:93953709-93961317 | NHDF-Ad | SE_44911 | chr9:93953704-93960917 | NHLF | SE_47822 | chr9:93954245-93954760 | Pancreas | SE_47822 | chr9:93954797-93956767 | Pancreas | SE_51473 | chr9:93953007-93961399 | Skeletal_Muscle | SE_52908 | chr9:93953760-93959405 | Small_Intestine | SE_65791 | chr9:93952890-93959470 | Pancreatic_islets | SE_66540 | chr9:93953161-93957016 | Jurkat | SE_67269 | chr9:93952624-93957244 | MM1S |
|
| 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 |
GH09I091191 | chr9 | 93953312 | 93962483 |
|
Enhancer Sequence | GCGCATGCGT GCACATCTGT GCTTCCTGGG AGCATAGGAA GTAGGAACCA GGATTTGTTT 60 CCATTCTTTT GAGACAGCAT TCCCATGGAG GTTAAAATAC AGTAAATGCT GAATGGAGAA 120 AGTTTCTAAT CCCCAGAATC GCAAATCCTA TTGGTGGGCA AATTGTTTTA AAAGAGCTGT 180 TTGGAGTTGA GGCGCACCTG CAAAATTAAA CACACCAGGG TGAGAAAGGC TTTCTGGGGG 240 CGGATCTGCA GGACTTGATT TTGCTGAGTT TAATGCCACT CATTTCACTT TCTGTTGGCC 300 AGAGCCCGTT TCCCCTGCTT GAAGGCACAG AACCTTGCTG GGAGCCAGGC AAGCTCTCTG 360 GACGGGATGG GCAGCCCCAG GGCCAGCCAT CCCAAGTCTA GGGCTTGCTG GGGCCTAGAC 420 TTTTGACCTC CAAAGGGTAC GGAGTCTGGG GACCACTCTG CACACCATCC TCCATCCAGA 480 GAGAGGGGCC ATTTCCATCC TCATTCGGTT TCCCATATTC AGGGGAACTC CTCTCCAAGA 540 AGAAACAAGG GCTCAGTTCC ATTTCTGACT TCTCTCTAGG TCAGCACGTG CGGTCACTTC 600 ACAGAAAAAT GGTGTGGATG TGCCAGACTG GGGACAAAGG CCCTCTGTTG TCCCCATTAC 660 CTGTGGTTTC CTGCCACAAA GGCTACACCA AGTACCTTAT AAAGAAGGGC TGAGCGCTTC 720 ATGGATTTAC TCAAAACCCA GCGCTCTGGG CTACTATGAC CCCAGCCACC AACAGGTGTT 780 GAGACTCCCC TGAGGCCCCG CCAAAACTGG CTGGGGTTTC CTCTCCACCT CAGTGCCACC 840 CCTGTCTCCA AGCCCATACT CCCAGGCATC TCTCAATCAC TACCTCTACA AGACCCCAGG 900 GTCTGGGTAA TGGGGGCTGG CAGAGCCTGG ACTCATTCCT GCAATGACGT CGGATACCAG 960 CGGCACCCAT TCCCTCTCCA AAGCTCATGT CCACAAGGGC AAACGATAGC ATCCCCCTCC 1020 ACCCCGGCAG TAAGCAGCAG CGAGTCTCAC CAATTTGAGA GTCTCTAGAA CAACAGATGG 1080 TAATTTGTTG ACACAAAGAT TTAAGGGGAC TCAATTACAG TCCCACTGAA AAAGCTCTCT 1140 CTAAAATAAG AAAGTATACA GATTCCTCAG CTCGCAGAAA TTGCTGACAG CTTTGTTTTC 1200 AACCCTCCAG GAGTAAAAAG AAGCTGACAA CTTATTTTTG CAGGTTATGC TCATTCAAGT 1260 CTATTTTTAG ATCTTGTTCC TAAATAAGTA CACCAGAATA GCATTCAGTT TGAAAATCAC 1320 CATCTGTTCA GAGCAATGAG CTTGGCCTCG CTGGGCTGGG TATACCTGGC CCATGGCAAG 1380 GTGGCAGTCC CCTTGTGGAC TGAACCGAGG GGGCAGTTTC AGGTCTCCAA GTGGTGTTTG 1440 AAGAATGCAC TAAAAACAGT CACAGGCAGT TGGCATTTTA AATGCCCATT AAACAACTAT 1500 TAATATATTT TATTTATAAG CTGAGAACCA CACAAAAAAT GCCCTTGGCT TTTTAAAAAG 1560 AAGTTCAAAT AATCCCTTGT ATTTAAATAG ATTTCTTATA AAAAGGCGAT CCAGCCTAAG 1620 TTTGGTAGTT AAGATAAAAA TTAACCTATG GAAAAGAAAG CCAGCTCAGA ACGCTATAAA 1680 AAGGCCCCTT CCCCCCCCCC CTTTCTTCCG GTGTATGGTG GCCCTCCCCT CCCTCTGCAG 1740 CCACTTGGTA GTGACTCACG CTTTTCTTTG GAAATGCAGT TGCTGCGTGA AACACAACGT 1800 GAGAATGGGA ATCTGACATA TGAGTAACCC GGCCGAGAGG CACCTCTTGG AAATGACACT 1860 GGGCCTTGGC TAGAATTACG CACAGGCCCT GGGAGGGCTG CGGCTCGTAG GCCCGTAGGG 1920 GGCAGGGTGA GGGCGGAGGT CCTGGCGCCC CCAGGCCTGA CCCGCCCGCA CCGCTGGGCT 1980 ATTTTTAGCG TCCACTAAAC TTAGCCGACT CCACCCTCTT GAATAACCCA CATCTTAAAA 2040 TGCTATTTTT CTCCAACAGG TCAAAAGAAT TCTGCGAGTT AGAGCGCAGA TTAAGTTGCT 2100 AGCGACGGGC ATTGAAGGTT TTAGAACCGA GAAAATGAGC CGGTGGCGGG GAGCGCGTCC 2160 TCAGCGGCCA GGCCCGGCAC GGGGCTCGGG CACTCGGGGA CACACGGTGG TCGTCGCTGT 2220 GTCTCAGCAG GACCCTGTGC GCTGGAGAGC TTGGGGCCGC GAGTCGCGCA GCAAGGAGGC 2280 TTCTGGCTTC TCTATTTTTA GCCTCTGAAC GTTTTCCAAA ATAATTACCA AAAGGAAATA 2340 CACACGCACA CATGGACCTA ACACACAAAA CGTCCTTCTG CGGGAAGCCA GCACTAGGAA 2400 AGAAAAAAAA AAAAATCCGA AGTGAAATTA TGACACAGGG TTTTGTAACC CGCGGTGGCG 2460 CGCTTCTGAA ACCCGAGCCC GGCAGCGGCT TCTTATCTGC ACCGCGTTCC AGGAAGCAGC 2520 CGGCGTTTCG GCCGCGCAAG GGCAGCCGCC GCACGTAGGC AGCGTCCCCC AGCCCGGGAC 2580 CCGCAGGAAT GCGAGGGGCA AGACAGATCG CCGGAGGAGC AGGGGTCAGA AGTCAGTGTT 2640 TAACCACTCA CTGGCTTTCG GTGAAGCCAG AATGTTAGCA GCGAGTCGCG GTCGGGGGCC 2700 TTGGGGTTGC ACACGCTTGC TCCAAGCACC GAGGCTCAGC TGAGCACATG CACAACCCTC 2760 TCGATGCAGC GGAAAGTCGT GTGGCTTAGG GCCGCACCCC GAATTTCGCC GCACCCGCCG 2820 CTGTGCCATT TACAACCCCC CACCCCGCCA CTGCTGTCAC GTAGCAATCA AGAGTAAAGG 2880 TTATCACAAA GTCTGTTCTT CGAAGGAAAG AGTTGGAATC AAGGACTTCG GACGGGAGGA 2940 AGTTGGTAAG TTACCGCTTC CTCCCTCCTG TTTTCCTCTC CTTGTTTAAC TTCTCACAAG 3000 AACATGTGGC AGCGCTGCAG GTTAACTCAT CTTACATAAC TTCGGGGCCG 3050
|