Tag | Content |
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EnhancerAtlas ID | HS193-00175 |
Organism | Homo sapiens |
Tissue/cell | U87 |
Coordinate | chr1:9359920-9361110 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOSL2 | MA0478.1 | chr1:9360370-9360381 | CTGAGTCACCC | - | 6.02 | JUNB | MA0490.1 | chr1:9360370-9360381 | CTGAGTCACCC | - | 6.02 | Myog | MA0500.1 | chr1:9361025-9361036 | GACAGCTGCAG | + | 6.62 | NFE2L1 | MA0089.2 | chr1:9360366-9360381 | TTTGCTGAGTCACCC | - | 6.88 | Nfe2l2 | MA0150.2 | chr1:9360368-9360383 | TGCTGAGTCACCCTA | - | 6.76 | Tcf12 | MA0521.1 | chr1:9361025-9361036 | GACAGCTGCAG | + | 6.14 | ZNF263 | MA0528.1 | chr1:9361064-9361085 | GAAGGATGGGGGTGAAGGGAA | + | 6.44 |
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| Number of super-enhancer constituents: 10 | ID | Coordinate | Tissue/cell |
SE_01570 | chr1:9359845-9363523 | Aorta | SE_23490 | chr1:9359796-9361335 | Colon_Crypt_1 | SE_23818 | chr1:9359897-9361251 | Colon_Crypt_2 | SE_24876 | chr1:9359985-9361543 | Colon_Crypt_3 | SE_26458 | chr1:9359877-9361291 | Duodenum_Smooth_Muscle | SE_26667 | chr1:9359663-9361407 | Esophagus | SE_32227 | chr1:9359984-9361097 | Gastric | SE_45049 | chr1:9359811-9361082 | NHLF | SE_50208 | chr1:9359830-9361115 | Sigmoid_Colon | SE_52461 | chr1:9359718-9361526 | Small_Intestine |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I009298 | chr1 | 9358616 | 9364232 |
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Enhancer Sequence | CTGAGGTGGG AGGATCGCTT GAGCCTAGGA GGTCAAGACT TGCAGTGAGC AGTGATTGTG 60 TTACTTTACT CCAACCTGGG CAACAGAGTA AGACCCTGTC TCAAAAAAAA AAAAAAAAAA 120 AGGGTCTCAT GCTGGTCCAT TACATTGATG TCATCATGCT TCATTGGACC TAGTGAGCAA 180 GAAGTCGCAA CCACTGTAGC CTTATTGGTA GGACATTTAC ATGTCAAGCG ATGGGAAATA 240 AATTCTACTG AAATTCGGGG ACCTTCTCCC TTAGTGAAAT TTCTCGGGGT CCAGTAGTGT 300 CAGGCCTGTG AAGGTATCCC CTCTAAGGTG AAGAATAAGT TGTTACAGCT TTCCTCCTGC 360 AACCAAGAAA GAGGCACAAT GCCTCGTGGG CCTGTTTGGA CTTTGGAGGC AACACATTCC 420 TCATTTGGGT GTGTTACTCC AGCCCATTTG CTGAGTCACC CTAACGCTTC TAGTTTTGAG 480 TGGGGCCCGT AGCAGAAGAC TGCAACAGGT CCAGGTTGCT GTGCAACCTG CTTTGCCACT 540 TGGGCCACCA GCAGATCCAG TGGTGGTTGA GGTCAGCGGC AGACAGGGAG GCTGCTTAAA 600 GCCTTTGGCA GGCCCCTGTA GATGAATCGC AGTACAGGCC TTGGGATTTT GGAGCAAGGC 660 CCTGCCATCA TCCACAAATA ACTTCATTCC TTTTGAGAGA CAGCTCTTGG CCTAATACTG 720 GACCCTAGTA GAGACTTAAT GTTTGACCAT CAGCCACGAA GTTGCCATGT GACCTGAGCT 780 GCCCATCATG AAGTGGGTGT TATCTATGAT CTGACCGACC AAACCAGACA TTGGGCATGT 840 GTGGCAGAAC GCTGCCATCG AGAGGAAGTG GTATATATGG GATCAGGTCT GAGCAGGTCC 900 TGAAGGCACA AGTAAGTGAC ATGAGGAAGT GGTCCAAAGG CCCATGGTTC TTACTTTGCC 960 CACTGCCTTC TCTCTCCAGC CTGTATCTAT GGTCTCCTGG GGAGTTCCCT CTGATCGATT 1020 GACAGTGGAA GAGAAGACTT AGTCAGCCTG GTTTGCAGAT GGCTACAGAT GGCTCTGCAC 1080 TATATGAAGG CACAACCCGA AAGTGGACAG CTGCAGCACT ATAGCCCCTT GCTGGGACAC 1140 CTCTGAAGGA TGGGGGTGAA GGGAAATCCT CCCTGGCAGA GCTTCGGGCA 1190
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