Tag | Content |
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EnhancerAtlas ID | HS076-04972 |
Organism | Homo sapiens |
Tissue/cell | H1 |
Coordinate | chr1:202007120-202008850 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
HNF4G | MA0484.1 | chr1:202008249-202008264 | TGACCTTTGACCTCA | - | 6.55 | NR2C2 | MA0504.1 | chr1:202008249-202008264 | TGACCTTTGACCTCA | - | 7.73 | Nr2f6(var.2) | MA0728.1 | chr1:202007811-202007826 | TGAACTCCTGACCTC | - | 6.22 | Nr2f6 | MA0677.1 | chr1:202008249-202008263 | TGACCTTTGACCTC | - | 8.42 | Rxra | MA0512.2 | chr1:202008249-202008263 | TGACCTTTGACCTC | - | 8.12 | TFAP4 | MA0691.1 | chr1:202007262-202007272 | ATCAGCTGTT | - | 6.02 | ZNF263 | MA0528.1 | chr1:202007393-202007414 | TTTTCCACCTCCTCTTTCTCC | - | 6.23 |
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| Number of super-enhancer constituents: 7 | ID | Coordinate | Tissue/cell |
SE_26730 | chr1:202006703-202007577 | Esophagus | SE_27624 | chr1:202002753-202007729 | Fetal_Intestine | SE_28545 | chr1:202005512-202007741 | Fetal_Intestine_Large | SE_31432 | chr1:202006127-202007611 | Gastric | SE_33417 | chr1:202002752-202008344 | H2171 | SE_52354 | chr1:202005643-202007598 | Small_Intestine | SE_67013 | chr1:202002752-202008344 | H2171 |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I202033 | chr1 | 202002815 | 202007566 |
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Enhancer Sequence | GATCCACAAC AGTACGAGGT CCCTTGGATG GCTTTGTTTG GGCACATTCC AAGCCTGCTG 60 GTGCCATTTT CCCACACCAG TCAGATAAGT GTGAGAAAAT GGCACCAGCA GGCTTCTAAT 120 GCAGCCCACA GATGGGCCAC CTATCAGCTG TTTGTCAGGT GTGTACAGAG CAGATGGCTA 180 GCCCTGTGTC AAAGGCCTGG GAGCACTAAG GCTCCCAGGA GAGCTCAGTG GCACCTGCTT 240 GGTTCTTTGG ATGGGGAGCT TGCATTTGAC CCCTTTTCCA CCTCCTCTTT CTCCTGTTCC 300 CAACGTGTGT CCTGAATTTC ACAGATTAGC AGATCTAGTT ATCCCCACAG ACAGAGATGA 360 GGGAGAAGTC CTCTGTTCTC ACAGCCTGTT GAATTTCCAT CTTTAGTCAC CCTGTACCAT 420 TGCCACATCT GCAGACATCC TAAATTCTAA TATATTTTAA TGTTTTCTAT TTATTTATTT 480 GTATTTTTTT GAGATGGAGT CTTGCTCTGT TGCCCAGGCT GGAGTGCAGT GGCACAATCT 540 TGGCTCACTG CAAACTCCTC CTCCTGGGTT CAAGTGATTC TCCTGTCTCA GCCTCCCAAG 600 TAGCTGGGAT TACAGGTGTG CGCCACCACA CTTAGCTAGT TTTTGTATTT TAAATAGAGA 660 CAGGGTTTTG CCATGTTGGC CAGGCTGGTC TTGAACTCCT GACCTCAAGT GATCCACCCA 720 CTTTGGCCTC CCAAAGTGTT GGGATTACAG GCATGAGCCA CTGCACCTAG CCTGATGTTT 780 TCTCTTTAAA TAGACTCCCC TTTACATCAT AAGTGAAACA AGTCAGACAT GAAAGAACAA 840 TTATTCTATG TGATACCTAG AATAGGCAAA TTTACAGAGA CAGAAAGTAG AATGGTGGTT 900 GGTAGGAGCT GTTAGGAGGG GATGTGGCGA GGCAAGAATG GGGAGCTAGT GTTTAATGGG 960 TACAGAGTTG CAGTTAGGGA AGATGAAAAT GTTCTGAAGA TGGGTGGTGG AAATGGCTGA 1020 ACCACAATGT GGCTATCCTT TTTTTATTAT TATTATTAAG ATGCAGTGTC TTGACCAGGC 1080 TGGAGTGCAG TGGTATGGCT CACCCCACCC TCAATCTCCT GGGCTCAAGT GACCTTTGAC 1140 CTCAGCCTCC CAAGTAGTTG GGACTACAGG CATGCACCAC CACACCCAGA TAATTTTTAG 1200 CTTTTGTATA GTGATGAGAT CTCCCTTTGT TGCCCAGGCT GGTCTCAAAC TCCTGGGTTC 1260 AAGTGATTCT CAGCCCTGCA AAGTGCTGGG ATTACAGGTG TGAGTCACCG TGCTCAGCCT 1320 CCACAATGTG AATATACTTT AATGCCACAG AACTGTTTTT TTAAAATGGG ACCTACAGCC 1380 AGGCGTGGTG GCTCACGCCT GTAATCCCAG CACTTTGGGA GGCCGAGGCA GGCAGATCAC 1440 GAGGTCAGGA GATCGACACC ATCCTGACTA ACATGGTGAA ACCTTGTCTT TACTAAAAAT 1500 ACAAAAAATT AGCTGGGCAT GGTGGCGGGT GCCTGTAGTC CCAGCTACAT TGGAGGCTGA 1560 GGCAGAAGAA TGGCGTGAAC CCTGGAGGTG GAGCTTGAAG TGAGCCAAGA CCGCACCACT 1620 GCACTCCAGC CTGGGTGACA GAGCGAGACT CTGTCTCAAA ATAAATAAAT AAATAAATAA 1680 ATAAAATGGG ATCTTCCAGA CAGCTGAATA CATGGAGGTT CCCAGAGGGT 1730
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