Tag | Content |
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EnhancerAtlas ID | HS048-30875 |
Organism | Homo sapiens |
Tissue/cell | Fetal_small_intestine |
Coordinate | chr6:2796930-2798350 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Myod1 | MA0499.1 | chr6:2797848-2797861 | TGCAGCTGTTCTT | + | 6.03 | ZNF263 | MA0528.1 | chr6:2798091-2798112 | TCCTCCTCCTCCTCCTCCTCT | - | 10.23 | ZNF263 | MA0528.1 | chr6:2798112-2798133 | TCCTCCTCCTCCTCCTCCTCT | - | 10.23 | ZNF263 | MA0528.1 | chr6:2798130-2798151 | TCTTCCTCCTCCTCCTCCTTC | - | 10.39 | ZNF263 | MA0528.1 | chr6:2798139-2798160 | TCCTCCTCCTTCTCCTCCTCC | - | 10.68 | ZNF263 | MA0528.1 | chr6:2798106-2798127 | TCCTCTTCCTCCTCCTCCTCC | - | 10.86 | ZNF263 | MA0528.1 | chr6:2798127-2798148 | TCCTCTTCCTCCTCCTCCTCC | - | 10.86 | ZNF263 | MA0528.1 | chr6:2798142-2798163 | TCCTCCTTCTCCTCCTCCTCC | - | 11.11 | ZNF263 | MA0528.1 | chr6:2798103-2798124 | TCCTCCTCTTCCTCCTCCTCC | - | 11.13 | ZNF263 | MA0528.1 | chr6:2798124-2798145 | TCCTCCTCTTCCTCCTCCTCC | - | 11.13 | ZNF263 | MA0528.1 | chr6:2798109-2798130 | TCTTCCTCCTCCTCCTCCTCC | - | 11.36 | ZNF263 | MA0528.1 | chr6:2798100-2798121 | TCCTCCTCCTCTTCCTCCTCC | - | 11.79 | ZNF263 | MA0528.1 | chr6:2798121-2798142 | TCCTCCTCCTCTTCCTCCTCC | - | 11.79 | ZNF263 | MA0528.1 | chr6:2798082-2798103 | TCCTCCTCCTCCTCCTCCTCC | - | 12.34 | ZNF263 | MA0528.1 | chr6:2798085-2798106 | TCCTCCTCCTCCTCCTCCTCC | - | 12.34 | ZNF263 | MA0528.1 | chr6:2798088-2798109 | TCCTCCTCCTCCTCCTCCTCC | - | 12.34 | ZNF263 | MA0528.1 | chr6:2797160-2797181 | AGGGCAGGAAGGAGGAGGGGG | + | 6.05 | ZNF263 | MA0528.1 | chr6:2798150-2798171 | CTCCTCCTCCTCCCCTGCTCC | - | 6.27 | ZNF263 | MA0528.1 | chr6:2798159-2798180 | CTCCCCTGCTCCTACTCCTCC | - | 7.15 | ZNF263 | MA0528.1 | chr6:2798168-2798189 | TCCTACTCCTCCCCTTCCTCC | - | 7.48 | ZNF263 | MA0528.1 | chr6:2798145-2798166 | TCCTTCTCCTCCTCCTCCCCT | - | 8.1 | ZNF263 | MA0528.1 | chr6:2798094-2798115 | TCCTCCTCCTCCTCCTCTTCC | - | 8.67 | ZNF263 | MA0528.1 | chr6:2798115-2798136 | TCCTCCTCCTCCTCCTCTTCC | - | 8.67 | ZNF263 | MA0528.1 | chr6:2798079-2798100 | ATCTCCTCCTCCTCCTCCTCC | - | 9.01 | ZNF263 | MA0528.1 | chr6:2798133-2798154 | TCCTCCTCCTCCTCCTTCTCC | - | 9.36 | ZNF263 | MA0528.1 | chr6:2798097-2798118 | TCCTCCTCCTCCTCTTCCTCC | - | 9.83 | ZNF263 | MA0528.1 | chr6:2798118-2798139 | TCCTCCTCCTCCTCTTCCTCC | - | 9.83 | ZNF263 | MA0528.1 | chr6:2798136-2798157 | TCCTCCTCCTCCTTCTCCTCC | - | 9.8 |
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| Number of super-enhancer constituents: 5 | ID | Coordinate | Tissue/cell |
SE_13330 | chr6:2796926-2799212 | CD34_Primary_RO01536 | SE_14198 | chr6:2797174-2798594 | CD34_Primary_RO01549 | SE_28080 | chr6:2797269-2798185 | Fetal_Intestine | SE_28996 | chr6:2796998-2798320 | Fetal_Intestine_Large | SE_49883 | chr6:2796919-2799305 | RPMI-8402 |
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| Number: 1 | ID | Chromosome | Start | End |
GH06I002795 | chr6 | 2795435 | 2798433 |
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Enhancer Sequence | TAAGTTATGC TCAAAGACTT TTGTGTCAGA ATGTCAGGGA AATGGATCAC ATGGTTCAGT 60 AACTGTCAGA TAATTTCAAA ACAGCACATC ACCTTCCCCA GGCTCTTCTC TTTCTCCTCA 120 AGTGCCTCAC TGGGACTCTC CTTCTCTTTT ATCTGGAAGC AGAGGCCTTG CAAGGGCTGG 180 CTGATCATCC CACAGTTCCA GCGTTTGCAG GGCAGCACTG GGCATTTTGA AGGGCAGGAA 240 GGAGGAGGGG GTGGGCTGCT CTTGCACCTC CCCTGTGCCC ACCTCCAGTC ACCAACCCAA 300 AAGCTGCTCT CTAGAGAACA AGTCCAGTCC TCTCTCATCT CCCTGCTGTT CCTCAATTTC 360 AAGTCTCTTT CATAAGGAAA TGTCCAAAGC TCTTGAAGGC TGGATGTCTC TCCACTGAGA 420 AGACTCTTAC TCAATTCAGA TGTCTATGAG GAAATCCCAT CACACCTTTT GCTCTGGGCC 480 CACCCATTCC TTCTGGATTT AGGGCCCTCG CGTAGGGAAG AGCCGCGTGG GACAGCCACA 540 CATGGTAGAG CCCGCAAGGG CAGCTCCAGG GTTGTGCTCT GTCTGCAGGA CCAAGGACAC 600 AAGGGAAGCC CCTTGGGGCA GCAAGTGGTC TTGGTGAATT GAGAAACTGA GGCCTCAGCA 660 CAGAAGGAAG GAAATGAGAG GAAGCTGGCC AGGTGTGACT CTGGGCTCAG TGGCCTGGAG 720 GCTCAGCACC AGATCCCTTC CTGCAGCTTC CCAGGCCTTC GCTAGCTCCT TCCAGCCAGG 780 AGTTTGAATG CTGGGTGGAC CAAGACACCT GAAGTTTCCT ACAGTGGCAA GGGTGGGAGA 840 GAAGGGGGTG GCCCTCAGTG ATGTAGTCCC TGGAAACTTA GGCAAGAACT GAGAATGAAT 900 GTGTCCTCGG CAGGACTGTG CAGCTGTTCT TCCCTCCCTG CTCCCCTCCC AGAACATGTG 960 ACAGGTGAAG TTCACAAGCA GCACATTCTT CACAGTTCCC AGGTCCCTGA AATCCCTTGA 1020 GACAGCCAAC AGCAAGCAAG GTGGGGAGGG ACGAAGTCCC AGAAATGACT TCACAAGAAT 1080 GTACACAAAC AACGAAGCCC CAATTTGAAT CTCACAGGTT CAGCCCTGGC CTGATCTCAC 1140 CCAAGGCAGA TCTCCTCCTC CTCCTCCTCC TCCTCCTCCT CTTCCTCCTC CTCCTCCTCC 1200 TCTTCCTCCT CCTCCTCCTT CTCCTCCTCC TCCCCTGCTC CTACTCCTCC CCTTCCTCCA 1260 TGCTGCCCTG GGCAGGCTGT GAGAGGAGAT GGGGAGAGAG CTGCTGTCAC TTTAAAATCA 1320 GCCTCTGCTG TGACTTCAAG CTAATCCATC AAACTAACTT CAAATGAATT CCTCCTCTCC 1380 ATTCAAATAT GTTTAAGCTC ACAGTTTCTT TTTCTTTGTC 1420
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