Tag | Content |
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EnhancerAtlas ID | HS039-03019 |
Organism | Homo sapiens |
Tissue/cell | ESC_NPC |
Coordinate | chr16:57307140-57307910 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
HNF4G | MA0484.1 | chr16:57307338-57307353 | TGACCTTTGACCTGT | - | 6.28 | NR2C2 | MA0504.1 | chr16:57307338-57307353 | TGACCTTTGACCTGT | - | 7.42 | Nr2f6 | MA0677.1 | chr16:57307338-57307352 | TGACCTTTGACCTG | - | 7.73 | Rxra | MA0512.2 | chr16:57307338-57307352 | TGACCTTTGACCTG | - | 7.58 |
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| Number of super-enhancer constituents: 9 | ID | Coordinate | Tissue/cell |
SE_03268 | chr16:57307172-57308032 | Brain_Angular_Gyrus | SE_04036 | chr16:57307002-57308082 | Brain_Anterior_Caudate | SE_04912 | chr16:57289251-57308755 | Brain_Cingulate_Gyrus | SE_05920 | chr16:57289682-57319783 | Brain_Hippocampus_Middle | SE_06780 | chr16:57289296-57308455 | Brain_Hippocampus_Middle_150 | SE_07898 | chr16:57292387-57308281 | Brain_Inferior_Temporal_Lobe | SE_27802 | chr16:57307069-57308006 | Fetal_Intestine | SE_28745 | chr16:57307051-57308098 | Fetal_Intestine_Large | SE_31625 | chr16:57307084-57308220 | Gastric |
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| 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 |
GH16I057273 | chr16 | 57307461 | 57307610 |
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Enhancer Sequence | CAGCCTGGGG GACAGAGCAA GACTCCATCT CAAAAAAAAA AAAGTTGGGG GGGCAATGCT 60 CCCATCCTGC CACCCTCACA CAGAGTGGCA GATGTGAAAA AGCTCATCTG GTGTCTGACC 120 CCAGCCCCAA ATAAAAGCTA GAACATCCCA GAACAGGCCT GTGTCTGTTC CCTAGCAGCT 180 CAGGATTTGG GCCCTGACTG ACCTTTGACC TGTCTCCCTG CCTGCAACTC CCTGTGAGAC 240 CCTGGGGTAC CACCCTGGCC TCTCCCCACT GGACAAACAG GAGAGACCAA CCCAGCCCAA 300 CAGCAAAGGG CCTGGGCCTG GCTTTTGTCA CAATCAGGGC TCAGCCCACT GGGCTGCCAA 360 GAAAGACAGC ACCCCCACCA CCCAGGTTCC CAATTACCAT GGAGACCTGG GCAAACAACA 420 GCCATGGGGA TCTGTCAGAT AATCTCTGAA TGGGAAATCA GGGTCCTAGT CCTCACCGAA 480 TTCTGCCACA AACAACTCAC TGGCTGATAA GGAGTGACCA ATGCCTGTCC CTGCCAGGTC 540 AACAGCAACA GCAACAGCCT GGGAGACTTT ATCCCAGTAC CCTGTTCTCC TTCCACTCAT 600 AGATGGTTGG GAAAATCACC CAAGGTCCCT CAGCCATAAC ACTGAACTCA AGGCTATTGC 660 TCCCTGCTGT GTGATCCTGG GGAAAGTGCC TTTCTCTCTC TGGGCCTGAG GACATTCAAG 720 TGCCACCTTC ATAGCTTTTG CCATATCCAC GAACGTGTAC TATTTTTTAT 770
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