Tag | Content |
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EnhancerAtlas ID | HS145-16447 |
Organism | Homo sapiens |
Tissue/cell | NHBE |
Coordinate | chr3:11602290-11603350 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
HOXA13 | MA0650.2 | chr3:11602616-11602627 | CCCAATAAAAC | + | 6.62 |
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| Number of super-enhancer constituents: 10 | ID | Coordinate | Tissue/cell |
SE_01661 | chr3:11599393-11603376 | Aorta | SE_03269 | chr3:11602443-11603332 | Brain_Angular_Gyrus | SE_04017 | chr3:11598170-11606165 | Brain_Anterior_Caudate | SE_05123 | chr3:11598234-11607875 | Brain_Cingulate_Gyrus | SE_06008 | chr3:11593611-11612723 | Brain_Hippocampus_Middle | SE_08645 | chr3:11596197-11613098 | Brain_Inferior_Temporal_Lobe | SE_38415 | chr3:11597975-11603248 | HUVEC | SE_41081 | chr3:11596380-11603438 | Left_Ventricle | SE_45564 | chr3:11602447-11603326 | Osteoblasts | SE_47146 | chr3:11587777-11606122 | Panc1 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr3 | 11602779 | 11603332 | chr3 | 11602762 | 11603096 |
|
| Number: 1 | ID | Chromosome | Start | End |
GH03I011560 | chr3 | 11601855 | 11603853 |
|
Enhancer Sequence | CAGAGAGAAC CCGGGCAGGT GGAGCTGGGC TGAATGTCCA CGTTCTGCCT GTGGACAGGG 60 CCTCGGGTGA GAGACTTCAC AATGCTGAGC AGACAGGCTC GGAAAGGGGG TTGGGGACCG 120 ACAGATGAGG CCTGGAGCAG ATCTCACACT GGCTGACCAC AGGGGTCAAG CAGCAGCAAG 180 AGAGCAGAAT ACCGAGACCT GGACACGCAC AGAGCCAGGA GGAAGGAGGG CCCTGCCCCT 240 GTCCAGCTCT CAGAGATGGC CAGGCCCTTC CTGAGCCTGG CTGCACCCAT GACCTTGGGC 300 TCTAGGAGAC CCCCCCCCAG GGTCCTCCCA ATAAAACTCC CTTTTGTGCT CAGCCGGCTT 360 GTTCTTTGCA GCGAGCGTGT CCTGACCCAC GCAAATGTGG GGAACTGGGG AGACATTTCG 420 AGCACAGGGA GGGGGAATCA AGGAAGATGA AGAAATGAGC TCACTGTCCA GCCTTTATGT 480 CAGTCTATCC AAGGCAGGAA AGGCCACTTC AGAAGAGACT CTCTAACAAG GGACCAGCAG 540 GGCAGGCTGG CTGACTGGTA TCAGACCACC TTCAGGGCAT CTCCTGACCT GAGCTGGGGC 600 GAATTGCCTT AACCGGTCAC CTGCAGATGT GAAGATGTTC AGTGTCTGGG CATCCTCTCC 660 TCCTCCCCAC AACCCAGGCT GCAGGGTGGC CCGTGAGCCC TCGTGGGACT GGCTCCACCA 720 CCCCTCCTCC CCAGCTGGAG TCAGGCATCT TGCCCCTGCC TCTGTGGTTG AGTGCAGGCT 780 GGGACTCGTC CACCTAGAAC GGGCCCCAGG CCTCCAGATG GTGAGCGTTT ATGGGATCCC 840 GAGGCTCCCC TCCCCCACAC CCTTATTTTC CAGATGGGGA AAATGAAGGC CAGAAACACC 900 CTGTTGGAAG TTACGCTGCG GATTTGTGGC AGGGCCAGTA TGAGCCCTGT CACTAACCCC 960 TTCACCCGCT GTCCCACCCA CCTGTGACTG TCCTCAGACA GAGGCTGCCC CGGGGGAGAG 1020 GGCTCCCACC ACCTCTCCTA TCTGAAAGCA ACCCCCAAGG 1060
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