Tag | Content |
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EnhancerAtlas ID | HS048-34066 |
Organism | Homo sapiens |
Tissue/cell | Fetal_small_intestine |
Coordinate | chr7:73172630-73173570 |
Target genes | Number: 14 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Nr2f6(var.2) | MA0728.1 | chr7:73173542-73173557 | GAGGTCAGGAGTTCA | + | 6.22 |
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| Number of super-enhancer constituents: 5 | ID | Coordinate | Tissue/cell |
SE_28553 | chr7:73172600-73173791 | Fetal_Intestine_Large | SE_47913 | chr7:73172737-73173614 | Pancreas | SE_50272 | chr7:73172568-73173785 | Sigmoid_Colon | SE_52703 | chr7:73172525-73173737 | Small_Intestine | SE_65463 | chr7:73172562-73173793 | Pancreatic_islets |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr7 | 73172917 | 73173261 | chr7 | 73172853 | 73173460 |
|
| Number: 1 | ID | Chromosome | Start | End |
GH07I073758 | chr7 | 73172612 | 73173594 |
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Enhancer Sequence | GTCGCCCAAG CTGGAGTTCA ATGGCGTGAT CACGGCTTAC TGCAGCCTCG ACCTCCTGGG 60 CTCAAACAAT CCTCCCACCT CAGCCTCCTG AGTAGCTGGG ACTACAGGCA TGCACCAACA 120 CATCTGGCTA ATTTTTGCAT TTTTTATAGA GACAGGGTGT TGCTTTGTTG CCCGGGCTGG 180 TCTTGAACTC CTGGCCTCAA GTGATCCTCC CATCTCTGCT TCCCAAAGTG CCAGGATTGC 240 AAGCGTGAGC CACTGCACCT GGCCAATACC CCTTCTTTTA TAGTTATGAG CTAGAGGCAG 300 CAAGTGACTT GGTCAAGGTC CCACAGTGGG CACCTGACAC CCATGCTCTT GCTCTCTCCT 360 GGCTCTGCAG AGCATTCTTG TCTCAGCATG GGTGACCTTT CGGGCAATCC TGGTATGGGA 420 GGGGGAAGGA AGGTACTATC TGTTCTTCCA GGCCAGCCAC AGACCTTGAG GGAGCCACAA 480 TAAACGCTGT GTTTGTTTGA TAAAGCAGTT GGCTTTTGGT CTGGCAGGAG GAAGAGCTGG 540 AACAGGTGTG GCAAGAGCGG GCAGCCTGCA GCACCTCTGT GGGAGATGGG TGAGACAGCC 600 CCAGGGCCTG GCAGGGGGCT CCAGGGCTGT GAGTTTTGAA GAAACCTAGG GACTTTCTCA 660 GCCATCTCTC TCATGTGGCA CCACCCCAGG GCCTGGCAGG GGGCTTTGTG GGTGTGGAGT 720 TTGAAGAAAC CTAGGGACTT TCTCACAACC TAGCCATCCC CCACGCGTGG CCACCTCTCT 780 CATGTGGCAC CACCCCAGGG CCTGGCAGCG CGCTCCAGGG CTGTGGAGTT TGAAAATCCC 840 AGGGACAGCC AGGCACGGTG GCTCACGCCT GTAATCCCAG CACTTTGGAA GGCCGAGGTG 900 GGCAGATCAC CTGAGGTCAG GAGTTCAAGA CCATCCTGGC 940
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