Tag | Content |
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EnhancerAtlas ID | HS180-04439 |
Organism | Homo sapiens |
Tissue/cell | Small_intestine |
Coordinate | chr1:211786360-211787760 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Atoh1 | MA0461.2 | chr1:211787419-211787429 | AACATATGTT | + | 6.02 | Atoh1 | MA0461.2 | chr1:211787419-211787429 | AACATATGTT | - | 6.02 | Foxd3 | MA0041.1 | chr1:211787631-211787643 | GTTTGTTTGTTT | + | 6.32 | HES2 | MA0616.2 | chr1:211787184-211787194 | GGCACGTGCC | + | 6.02 | HES2 | MA0616.2 | chr1:211787184-211787194 | GGCACGTGCC | - | 6.02 | NFE2L1 | MA0089.2 | chr1:211786845-211786860 | GCATGAGTCAGCAGA | + | 6.21 | Nfe2l2 | MA0150.2 | chr1:211786843-211786858 | GAGCATGAGTCAGCA | + | 6.66 | PRDM1 | MA0508.2 | chr1:211787511-211787521 | TCACTTTCAC | + | 6.02 |
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| Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
SE_28267 | chr1:211786043-211787790 | Fetal_Intestine | SE_29189 | chr1:211786057-211788707 | Fetal_Intestine_Large | SE_54270 | chr1:211786127-211787593 | Spleen |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I211610 | chr1 | 211784144 | 211788437 |
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Enhancer Sequence | AGTGAGCAAT GCCCAGGGCC TACAAAGCCT GTTCCCGTGC AAACTCGGCT ACTGGCTGGT 60 GCTGTGCTTC CTGCCCTGCA GGCTGGGCGC CTTGAGGGTT CTGCATCCTC CTCCTCACCA 120 CTACCAACAG CTTCTCATCT GGCAACTGGG TGGAGATCCT GCGGACCCCG CTGGACCACT 180 GTAAGAAGAG CTTCACCTCA GCCTTGCTCT CTGACCAAAA CTGACAGGCC ACCATTTTGA 240 AATGCTGACA CATCCAGAAG TGACAGAATG GAAACTCCAG CACTCTCTGG GCACCAGTCA 300 GTGTCCAGCA CTGTTACTTC AGGGTCTGTG AGGAGAGTGC TGGTGGCGTG AGAGTGAGAA 360 TGAGGGGTAG GGCAGCAGGC TTGTAGTCAA ACTGCCTTAG AGAAAGACAC CATGAGCGTC 420 CCAGGAAGAG GCTATTAATA GGCCTCCCTG AACATGCTCA GCGGTCCTGG GCTGGGGCTG 480 TGAGAGCATG AGTCAGCAGA TGGAAGGGCT GATGGTGAGC CCAGGACACA GAGCCAGCTC 540 CCCACAGGGG AAGTGGAGGC TGTGAGACTG CACTTTTGAG CAACCCTGGT CTCGTGCCGC 600 CCCACCCTCT TTTGAGTATG TAATCTGTTT GGATGGTATA TTACCAGTGT TGTAAATTCC 660 AATTCTGGAG CCAGAATTTT TTTTTTTTTT TTTTTTTTAA GAGACAGAGT TTCACTCTGT 720 CACCCAGGCT GGAATGCAGT GGTGCAATCC TGGCTCACTG CAGCCTCAAC CTCCTGGGCT 780 CAAGCAATCC TCCCACCTCA GCCTCCCAAA TAGCTGGGAC TACAGGCACG TGCCACTATG 840 CCTGGCTAAT TTTGAAGCCA GAATTTAAAG CAGCAAAAAA TCCAGAAAAT CCTTTCCCCC 900 CACTTACCCT CTCTTACTTT CTCTTCATTG ACAAAGCTGG GCACAGGAAA AAGGACTCCA 960 TCCCCTGCAA TGTGAAGGGC TGCTCAGCCA TTATGAATGC CCCTCTCCAC ACCTACCCAG 1020 CCACTGACTC ACTCCGGGAC GAGCTCCCAA TGTAGATTAA ACATATGTTG AGTGCCAGGC 1080 CCTGTGACGG GCGGTTTCAC ACATATTATC TCATCCTCAT AATGACCCCG GGACACAGAT 1140 ATATTGATAT CTCACTTTCA CAGATGAAGA ATCAAAGCTG AGAGTGATTA AGCTATTTGT 1200 CCAAGGAGCT GTAGCCACTG TCATTTATCA AGTATCTAAC AGATGCCAGG GACTTGCATA 1260 CAGTTTTTTC TGTTTGTTTG TTTTTGAGAC AGAGTTTCCC TCTTGTTGCC CAGGCTGGAG 1320 TGCAGTGGCA CACTCTTGGC TCACTGCAAC CTCCGCCTCC CAGGTTCAAG CAATTCTCCT 1380 GCCTCAGCCT CCTGAGTAGC 1400
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