Tag | Content |
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EnhancerAtlas ID | HS164-04006 |
Organism | Homo sapiens |
Tissue/cell | Raji |
Coordinate | chr14:92866800-92868180 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Foxq1 | MA0040.1 | chr14:92867675-92867686 | CATTGTTTATT | + | 6.02 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_09545 | chr14:92862428-92879109 | CD14 |
|
| Number: 1 | ID | Chromosome | Start | End |
GH14I092396 | chr14 | 92863156 | 92868179 |
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Enhancer Sequence | AAGAGTTGGG GGAAAAATAC ATACACACAG CCGGAGTGCA GTGAAATGAG GGAGAGAAGA 60 TCTATAAGGG ATTGACTAAG AAGCTCTGGA CACAGTCGCC TTCTTTGGGG CATGCAGGAC 120 TACGGTTCTT TTTACCCTTG ACTTTGAACC CCAGTTAGGC ATGCCCATCC CTCTCTGGGA 180 AAGTATTGAG TAATTATAAC TGAGAATGTA ATCCTCTTTC AGATGAGACC ATGTCGTAAT 240 TAGCTGCAAT GATAGGAAGT TAATTCATTT GGTTCCCTCT GACAGGTCTG AAACTAGCCT 300 AAGCACGTGG GTCCCCTGTT ATCTTTGCCT TTTCTTGTTT ATTTCTGTAA GCATTGGTGT 360 TTTGTGGGAG ATGCATACTT TGCATATGCA AGATAGAAAG AGCTTTTGTC AACACTGTTG 420 ATGCCTGGTG TAAACAAGCA TGTTTGAAGA GTTACTGACG AAAGGCAGAA GATAAATTTC 480 AACATGTGCT TTTGCTTGAG AGGAAAAATC AGGAAATGAG AGTGAAAGCT GAAGTGAAAG 540 AGATTCTTCT GAAAGTGTCT TCATTTCATG GAGAGGGGGG AATACACACA AGGCACCCAG 600 TATCTGGCAG TCCTTGCTTC TCCACCAGCA AGGCAGGAGG ACACAATAAA GAGAAAAGAC 660 TACAGCTCAT CCCCCTGTCT CATAAGGAAG AGTCTGAAAA CCCCTGCCTC TTAGAGTTGA 720 CTTAGCCAGC AACACTTGCA AATCAAGTCG ATAAGAATTT TTTGCGCCCC ATTGTGTGCC 780 TGCTGCTGTG CTGGTAGATA GGGGAGGGCA CCAAATGGAA AAACCGTGCA GGTTGTGCAC 840 TGCACAATCC TAGAAGGTGC TGTTCAAACC ATAGACATTG TTTATTTGTC TCTTTAGTAT 900 GATAATATTC CAGCAAATGG AAGCAAAATG TCTTGAGGAA GACTTTTTCT ATTTCTTGGC 960 ATCCTGTGGG CTAGTATGGC CTAAATGTGG AGATGAACAG AGAAACAACC ATAGTACATC 1020 ATGATAATGG CCAGAGTGCA TGTGTGTGCA AAGCACAGAA GGACTTAGAA GGAACCCTCC 1080 ATGTGCCTAA GAGTCATGCA GTGGTTCACA AAGGGCCCCT CTTTGGAAGA CTATTCCCCT 1140 GAGCAGAGAG AGGCAGTGTT GTGGAGTGGC AATGAGATTG TGTTTTACAC CCAGACTGCC 1200 TGGGTTCAAA TCGCTAATGT GCTCCTTCAC ATGTGACCTT GGGCGAGTTA TCTAACCTCT 1260 CTGTCCCCTA CATGAGTTGC TGCTGTTTCC GCAGTGCCCT GAGGTGTGTC TGCCCAGCCA 1320 GGCTGTAGTT TAGGAATGTA GTGTTGGGGG CAGGGAGGCA TCTCAGTCCT AATACACTCA 1380
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