Tag | Content |
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EnhancerAtlas ID | HS180-35393 |
Organism | Homo sapiens |
Tissue/cell | Small_intestine |
Coordinate | chr3:188114290-188116360 |
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) |
NFIC | MA0161.2 | chr3:188114862-188114873 | TTCTTGGCAGA | + | 6.02 | Nr2f6(var.2) | MA0728.1 | chr3:188115620-188115635 | TGAACTCCTGACCTC | - | 6.22 |
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| Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
SE_10588 | chr3:188114016-188120045 | CD19_Primary | SE_10953 | chr3:188113668-188122274 | CD20 | SE_60963 | chr3:188056356-188170886 | HBL1 |
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| Number: 1 | ID | Chromosome | Start | End |
GH03I188396 | chr3 | 188114173 | 188116501 |
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Enhancer Sequence | TGCAGTTAAC TTGCAGACTT ACACAGTTAT TGGTAGGTTT AGAAATAGAA GATGCTAGAT 60 AACCGTTAAA GAGATTGCTA GGTCTCATTA GAGATCATAT TGGTGATTTT TCCTATCGTC 120 ACTTTTTCCT GGGTGAGGGG CAAAATCTTT ATGAATTAGG CACTTAGCGT CTCACCTTTA 180 CAAATCCAGA TTTCCACCTT TAGAAGCAGA TTTACTGAAC TCAAAGAGGT GCAGGCTATT 240 GTTGCCTGTT TTCTCTTGGC CTTGAACAGA AAAGCAGTCT ATAATAATCA AGGACTTAGA 300 AGAAACCTGC TAAGGAGCCC GTTTTTTTGC CAGCACTGCA CACTCCACAG ACTAGCCATA 360 ACATTGTGGA TCATAAGAAG TTGTGGGAGG AGATTTTGAA GGTCATCATT AGTTGCTTAT 420 TATTTTAAAT CTGCAGAAAC TGAGGTCCAG AGAGAATTCA CATTTTCTTG GTTACTTTGC 480 CACGTGGAAC AATTGTTATC AAATGTGACC TGGAATGCAA GGTTGGGGCC ATTTATCTTC 540 TGTGCTAATT TTCAGTGCCA TGGTTGCGAA CTTTCTTGGC AGAGAAATTG TTTACTTCTG 600 TGCCCTATTC CATTGCCTTT TACCTACCCC ATCTAGTTAT AATCTAGCAA TAGAGTTATA 660 AGCTTGTGTA ATCAAACTTT CCCACTGCAG ATGCTCTTTG GAGACAGAAT ATTTGGGTTT 720 AAACCCAGCC TCTGATATGT TCTAGCTGCT CTATTACATT GGATAAGTTT CTTTAGCTTC 780 TCTAAATCTC GGTATTTGAA TACTCAAATT AGAAGACGTA AATTATTTCC TAAGATTTCT 840 CCTAGCTGGG GTTCTCTATG ACCTTTTAGC TCTTAAGTAG TCTGTCCTGG CTATTGTCAA 900 CCATGTCTTT TTTTCCTTGA CTGATAGAAA CTGTGGCAAA CTAAAGGCCA CTTAGTCAGT 960 ATTTGTTCCG TCCTTAACCT TCTCTCCTGA GAGTCCTGAT CTTTCAGTGC TGTTGTTTCC 1020 CTGTCAGGGT TGATTGTTTC CTTTTCGAGT GCCGTTCTGA ATCTGAAGTG AAAGTGCAGC 1080 GTGGAGGCAT GTCACTGTTG TGTCTCACTT CTTTTTCTTT TTTTTTTTTG AGATGGAGTT 1140 TCACCCTGTC TCCCAGGCTG GAGTGCAGTG GCGCGATCTC GGCTCACTGC AACCTCTGCC 1200 TCCTGGGTTC AAGTGATTCT CCTGCCTTAG CCTCCCAAGT AGCTGGGACT ACAGGTGTGC 1260 ACCTCTGTGC TCGGCTAATT TTTGTATTTG TAGTTGAGAA GGGGTTTCAA CATGTTGGCC 1320 ATGCTGATCT TGAACTCCTG ACCTCAAACG ATCTGCCTTC CTCGGCCTCC CAAAGTGCTG 1380 GGATTACAGG TCTGAGCCAC TGGGCCCGGC CGTGTCTCAC TTCTTTATCT GAGACAATGT 1440 TTACTGGTCT AGACCTGATG CTTCTCTCCC TTGCTGCTTC GTAGTTTATT TGGATCCTGA 1500 AATGCCGCTG AGTTTTTCTT GTCACCTGCA GCATTGCCAA GAACAAGGAG TGCACCATTA 1560 GTGTTAATTT ATTTTTTCTG GTACTCTGTG CAAGGCAGAT GGGCATTTAA TGTGCTGATT 1620 CCAACCCTAC CTTCCCTCAT CTACACTCCC TGGTCTCATA GGAGTTAAAA CATAGTTTTG 1680 TAAGAAACCT TAGCTCCTTG AACTTGTGGA CTTGTGGGAG AATCATGGAA ACATGAGAGT 1740 TAGAGGGAAT GGTAGTGGAT ATCTAATCTT TAGTGTACAG ATAGGAAGGG TCACTGAGGT 1800 TCAAAGAGGT TAAGAACGAA AGTCATAGAC CCAATTAGTG ACTGAGCTAG ATAGAAAGTA 1860 CGCCCAAGTC CTCTGCATCT AAGTCTAGTG CCTTTTCCAG TTTTTCCAAA TGTCTCTCAG 1920 ATAGCCTATA TAAAGGTTTG GCATTTCTGT AGCGTTGTTC TCTCGTTACC TCTTCTGAGC 1980 AATGCCAGCT GTCCATGCAG AGAGTGGGGC ACTTAGCCAG TGCTGGGCCA AAGCTGTCTG 2040 TAAGAAGAAG TTGAGTGAAT ACATTGACAT 2070
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