Tag | Content |
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EnhancerAtlas ID | HS034-14837 |
Organism | Homo sapiens |
Tissue/cell | ECC-1 |
Coordinate | chr19:16208460-16209500 |
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 | CATCCTACCA CCACTACCAC CTCAAATTAT CACAGATAAT TGACATTTAG ATGTTCAAGC 60 CACATCTTCC AGACTACCCC TTGAACCTGG AAATGGCATG AAAATCTCCA ACTAGATCCT 120 GAATTTTCGG TATCCATTGT TATTCCTCAT CCTATTTTTT TGTCCAGGTG GGAAGCTCTG 180 TCCCCATTAC TCTCTCTATT CATCCATTCC TCCAAAATGC ACCTCCCCTA AACCACCTCC 240 ACCTTTCCAC CCTCAGCCTC TCCCTGCTCC TAACTGCCGT CCATCCTGAA CTTCTGCAAA 300 AACCATTCCC CTCACACATT GCCATATATA TGCCCTTGGA AAGATTACAG ACTGTGTAGG 360 GGGCTGGTTT TTGTTTGGAG TCTGTGTGTT TGTCCCTGGA ATTTCTCCAG GCATTTCTGG 420 ACTCCACCCT TTGAAGTAAC TATGCAGCCT GTCTATCCAG TTATTCTACC TAACTAAGCA 480 CATAAGTGGA ATTTCAGAGA TTAGTGCTAT GGCCGGGCAC GGTGGCTCAC GCCTGTAATC 540 CCAACACTTT GGGAGGCCAA GGCAGGCAGG TCACTTGAGG TCAGAAGTTC AGGACCAACC 600 TGGTCAACAT GGTGAAACTC TGTCTCTACT AAAAATGCAA AAATTAGCCG GGCATGGTCA 660 TGGGGGCCTG TAATCCCAGC TACTGGGGAG GCTGAGGTGG GAAAATCAAT CACTTGAACC 720 TGGGAGGCGG AGCTTGCTGT GAGCCAAGGT CGAACCTTTG TACTCCAGCC TGGGCGACAG 780 AGTGAGACTC CGCCTCAAAA AAAAAGAAAA GAAAAGAAAA GAGATTAGCA CTATGGAGGT 840 CTACACTATC TGTTGATAGT CTGTGAGCCT TGTCGTGATT CTCAAGGGCA GTTAACACTT 900 TCAGGGAAAG TCATTTTATC TCAGACCTAA TAACAAAATA GATGCTAAAG CATCTGAGTG 960 ACAAGATGAA GCGAAGTCAG GATTTGTAGT CAAGAGACCA GGGTTTAAGG CCTGGCGCAG 1020 TGGCTCACAC TTGTAATCCC 1040
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