Tag | Content |
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EnhancerAtlas ID | HS073-09543 |
Organism | Homo sapiens |
Tissue/cell | GM19238 |
Coordinate | chr21:43888640-43890070 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Hnf4a | MA0114.3 | chr21:43889712-43889728 | AGGTTCAAAGTGCACT | + | 6.15 | RREB1 | MA0073.1 | chr21:43889469-43889489 | GTGGATGTGGTGGTTTGGGT | - | 6.46 |
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| Number of super-enhancer constituents: 7 | ID | Coordinate | Tissue/cell |
SE_23711 | chr21:43888349-43890143 | Colon_Crypt_1 | SE_24218 | chr21:43888785-43889542 | Colon_Crypt_2 | SE_27810 | chr21:43886897-43891053 | Fetal_Intestine | SE_28739 | chr21:43887048-43891008 | Fetal_Intestine_Large | SE_50898 | chr21:43888275-43890234 | Sigmoid_Colon | SE_52661 | chr21:43888347-43890669 | Small_Intestine | SE_59589 | chr21:43879292-43899707 | Ly3 |
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| Number: 1 | ID | Chromosome | Start | End |
GH21I042466 | chr21 | 43886847 | 43890842 |
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Enhancer Sequence | AGCCCATGGT GACTATGCAA AAAAGATCCA GAACAAAGGG ACTTGTCACC TTTGAAGCAT 60 CTGCTAAACT AACACCTCGC TTATAAAATT GGTCATACAA GGGAAAGAAT GAAAGGTTTT 120 ATTCTGTTTT TCTAGGAGGA GCTGCATTTC ATGGGAACCA AATAAATCCA TGATTTACAG 180 CCTAATAAAT TCAGAAGGAA CAGTGGAGTT GGAAAAACAC CATCTCGCAA ACCATACTTG 240 TAGTGGGCTG AATCATGACC GCAAAGATAT CAGGCCCTAA TCGTTATCTG GGGTTAACTA 300 ACAGTGGATC AACCAGATAG GCTATGCCTT AGGCTGTAAT GAAGGAGGAA GTCTGTAACA 360 CCACAAATGT GAATTCCAGC TAAGAACATT ACCGTGAATC CACCAAACCT TTAGCTCCAG 420 CTTCTTTGGC AGTAAGAAGT GCCCAGAGCT TAAAGAACAA GAGAGCCCAG ACAAGCCCAG 480 AAGATGAGAT ATTCTGCCAG GCAGCCCGCC CAGTCCCTTC AAAGCCAGCA ACATGAAAGG 540 GACTGCACTG AATGAAAAGA ATGGGGTGCA GGGATTTCCA TGAAGCTGAC AGCCTCCAGC 600 TTCAGACTCT GCACAGGCAC AGGCCCCTTG CAAGGTCCAG ACAGGGTGTC CACCTGGCCC 660 TGTGTTTCAT CTATTTTGCA TTAGTGAAGG ATTTTAACCA TAATCGTGCC TCTGCCACTT 720 TCCCCTCTAA TTTCAATCAG ACATGTGTCC CCTCAGGTGG AAGGGCATTG AAGTGGCCAC 780 AGGCACTTTT AGAATCTGTT TCAGGGGCAC TAATTGAATT GAATCAAGGG TGGATGTGGT 840 GGTTTGGGTT CCAGAGAGTA TTTGTGTATG CCACTGGTTT GCAGTAATTT TCATATGTAG 900 TACAGTTTCT GCCACCTGTC CTGGAGTAGT ATCACTTCCA GAAATACTTC TAACACTCAT 960 TTTGCTACTT ACCTAGAATT GAGACACGTA AGTGCAGGGT CAAACTTCAA ATCCCAGTAT 1020 GAACCTGTCC TCCAGCTCCA GCACCATTGC GTGTGGGAGT GCAGAAGAAA TTAGGTTCAA 1080 AGTGCACTGA GTCAGAAGCT GGGCTATGGA GATCATTTCA ATCATCAGAA GTGGAAAACT 1140 GTAAGAGTGC GCTGATGCCT GCTTCTAACC AGAATATCTC CTGTCAGGGG CGTAATGATA 1200 TATCATATAT ATTTTTTTCT TTTTTTGAGA CTGGGTCTCA ACTCTATTGC CCAGGCTGGA 1260 GTGCAGTGGT GCGATCACAG CTCACTACAG CCTCAACCTC CTGGGCTCAA GTGATCATCC 1320 TGCCTCAGCC TCCTGAGTAG CCAGAATACC AGGCTAATCT TTGTATTTTT TGTAGAGATG 1380 GGGTCTTGCT ATGTTGCCCA GCTGGTCTTG AACTCCTGGT GCTCAAGTAA 1430
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