Tag | Content |
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EnhancerAtlas ID | HS180-23958 |
Organism | Homo sapiens |
Tissue/cell | Small_intestine |
Coordinate | chr19:16208410-16209560 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Nr2f6(var.2) | MA0728.1 | chr19:16209036-16209051 | GAGGTCAGAAGTTCA | + | 6.38 | RARA | MA0729.1 | chr19:16209036-16209054 | GAGGTCAGAAGTTCAGGA | + | 6.05 | ZNF263 | MA0528.1 | chr19:16208709-16208730 | CCCTCAGCCTCTCCCTGCTCC | - | 6.66 |
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| Number of super-enhancer constituents: 10 | ID | Coordinate | Tissue/cell |
SE_23280 | chr19:16208506-16208969 | Colon_Crypt_1 | SE_24812 | chr19:16208468-16209144 | Colon_Crypt_3 | SE_26678 | chr19:16208277-16209524 | Esophagus | SE_27889 | chr19:16208269-16209129 | Fetal_Intestine | SE_28973 | chr19:16208302-16209223 | Fetal_Intestine_Large | SE_31734 | chr19:16208416-16209401 | Gastric | SE_35489 | chr19:16208226-16209840 | HepG2 | SE_46221 | chr19:16208245-16209704 | Osteoblasts | SE_52442 | chr19:16208317-16209080 | Small_Intestine | SE_62472 | chr19:16180149-16231639 | Tonsil |
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| Number: 1 | ID | Chromosome | Start | End |
GH19I016091 | chr19 | 16202245 | 16209891 |
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Enhancer Sequence | ACATACCAAT TTGTCCCAAA ATTTCAAATA GTGCATCTGG TTCTCCCCTG CATCCTACCA 60 CCACTACCAC CTCAAATTAT CACAGATAAT TGACATTTAG ATGTTCAAGC CACATCTTCC 120 AGACTACCCC TTGAACCTGG AAATGGCATG AAAATCTCCA ACTAGATCCT GAATTTTCGG 180 TATCCATTGT TATTCCTCAT CCTATTTTTT TGTCCAGGTG GGAAGCTCTG TCCCCATTAC 240 TCTCTCTATT CATCCATTCC TCCAAAATGC ACCTCCCCTA AACCACCTCC ACCTTTCCAC 300 CCTCAGCCTC TCCCTGCTCC TAACTGCCGT CCATCCTGAA CTTCTGCAAA AACCATTCCC 360 CTCACACATT GCCATATATA TGCCCTTGGA AAGATTACAG ACTGTGTAGG GGGCTGGTTT 420 TTGTTTGGAG TCTGTGTGTT TGTCCCTGGA ATTTCTCCAG GCATTTCTGG ACTCCACCCT 480 TTGAAGTAAC TATGCAGCCT GTCTATCCAG TTATTCTACC TAACTAAGCA CATAAGTGGA 540 ATTTCAGAGA TTAGTGCTAT GGCCGGGCAC GGTGGCTCAC GCCTGTAATC CCAACACTTT 600 GGGAGGCCAA GGCAGGCAGG TCACTTGAGG TCAGAAGTTC AGGACCAACC TGGTCAACAT 660 GGTGAAACTC TGTCTCTACT AAAAATGCAA AAATTAGCCG GGCATGGTCA TGGGGGCCTG 720 TAATCCCAGC TACTGGGGAG GCTGAGGTGG GAAAATCAAT CACTTGAACC TGGGAGGCGG 780 AGCTTGCTGT GAGCCAAGGT CGAACCTTTG TACTCCAGCC TGGGCGACAG AGTGAGACTC 840 CGCCTCAAAA AAAAAGAAAA GAAAAGAAAA GAGATTAGCA CTATGGAGGT CTACACTATC 900 TGTTGATAGT CTGTGAGCCT TGTCGTGATT CTCAAGGGCA GTTAACACTT TCAGGGAAAG 960 TCATTTTATC TCAGACCTAA TAACAAAATA GATGCTAAAG CATCTGAGTG ACAAGATGAA 1020 GCGAAGTCAG GATTTGTAGT CAAGAGACCA GGGTTTAAGG CCTGGCGCAG TGGCTCACAC 1080 TTGTAATCCC AGCACTTTGG GAGGCCAAGG CAGGCGGATC ACTTGAGCTC AGGAGTTTGA 1140 GACCAATCTG 1150
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