Tag | Content |
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EnhancerAtlas ID | HS173-00115 |
Organism | Homo sapiens |
Tissue/cell | SH-SY5Y |
Coordinate | chr1:17923360-17924490 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CDX2 | MA0465.1 | chr1:17923769-17923780 | TTTTATGGCTC | - | 6.14 | TCF3 | MA0522.2 | chr1:17924083-17924093 | AACACCTGCT | + | 6.02 | ZNF263 | MA0528.1 | chr1:17923586-17923607 | CTTTCCTCTCTTCCCTGCTTC | - | 6.5 |
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| Number of super-enhancer constituents: 13 | ID | Coordinate | Tissue/cell |
SE_01537 | chr1:17921744-17927542 | Aorta | SE_23081 | chr1:17921201-17925643 | Colon_Crypt_1 | SE_23747 | chr1:17921758-17924697 | Colon_Crypt_2 | SE_24767 | chr1:17921216-17924712 | Colon_Crypt_3 | SE_26139 | chr1:17921977-17924812 | Duodenum_Smooth_Muscle | SE_26573 | chr1:17921957-17923982 | Esophagus | SE_28131 | chr1:17921123-17925727 | Fetal_Intestine | SE_29073 | chr1:17920969-17925491 | Fetal_Intestine_Large | SE_50079 | chr1:17921723-17925480 | Sigmoid_Colon | SE_52601 | chr1:17921731-17924732 | Small_Intestine | SE_57000 | chr1:17921741-17924705 | VACO_400 | SE_65277 | chr1:17921749-17924817 | Pancreatic_islets | SE_68684 | chr1:17922816-17924643 | H9 |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I017593 | chr1 | 17920434 | 17925458 |
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Enhancer Sequence | ACATGATGAA ACCCTGTCTC AACTAAAAAT ACAAAAAAAA GTAGATGGGC GTGGTGGCAC 60 ACGGGGACCT ACCCCTCCCT GCCCTGCTGC TCTTTGGAGA GAGAAGAGGT GGGGCACAAA 120 GGTGCTTGGA GCTCTGTGGA CCAGAAACGC ACCAGGTGGC CTTCTGGTGC ACTTGAACTC 180 CTCTGCCGGC AATGTAGGTT GCTGCTTGGG GGTGCTGGGA GGGGTCCTTT CCTCTCTTCC 240 CTGCTTCTGC ATCTGCTTCT GCCTTTTCCT CCCCATCTCC TGCCCCTCAC CATGGATTCA 300 GCTTCTTTCC TTTGCATTCA GGTTGCTGGC CTTACTCTCA TTTGCAAGCT GAGAGGCATT 360 AGGAGAGCAG GAAGCTCAGA TAAGGGTGAG ATAATTGCCT CTTACTGGTT TTTATGGCTC 420 TTTTATGACC CGGAGGCCCC TGAAGGAGTG TTTGTTCACA GGGAGAATTA GACACGGCAG 480 CCCTGCGTGG CTTCCATGGA CAGCGGCTGG GAGAGGCTGC TCCGGGTGGG TACAGGGTGG 540 GTCCAGGGCC TTGGCAGGCA TCAGGGAGGG TCACGGGTAC AGGAGGGGCC CCCAGCCTCA 600 TTTCTTGCCG TGCCCTCTTT GCATGCGTGT CTTGAGCTGG AACGTTGCTC GTGTCCCTGC 660 TCCCCCAACT TTATTCCTCT TCCCCTGCCT GGGAAGCCCT TTCCCCATCT CATCGGCCCG 720 AGGAACACCT GCTCCAGTCT AGGGAGGCAG CGGAGGTGGT CCTGAGAGCA AGGCTTTGCA 780 GATAGATCAC CGGGGTTCAA ACTGCCGCTG TGCCACTTGC TGGTCAGGTG ACTTGGGTAG 840 TGGGGGTGGG CAGGAAGTGA CCTCTCTATG CTGTGGGGAC CCCCATTCCC CAGCCCAGTA 900 CACCAGAGCC AGTACCTGGG CTGGTCGCTC ACTGGGTTTT GATAAGGTGC AGCGAGGAGG 960 AGCCTCCCCC TGCCTATGAG TCGGCTCATC AGGTGTTTCC AAATCCCTCC TGAAGTTGCC 1020 TGACCTCACC CAGTGATGCC TCTGCCCACC TCCACGTCAC CTTTACAGTT TACATGGGGC 1080 TTTCTCTGGT GTTCTCTTGG TTAAACTGCA TTCTTTCGGT TAAAGCGTGC 1130
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