Tag | Content |
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EnhancerAtlas ID | HS094-23433 |
Organism | Homo sapiens |
Tissue/cell | hMADS-3 |
Coordinate | chr2:228315600-228316960 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
MEF2A | MA0052.3 | chr2:228316769-228316781 | TCTATTTTTAGT | - | 6.27 | MEF2B | MA0660.1 | chr2:228316769-228316781 | TCTATTTTTAGT | - | 6.32 | MEF2C | MA0497.1 | chr2:228316768-228316783 | TTCTATTTTTAGTAG | - | 6.57 | Nr2f6(var.2) | MA0728.1 | chr2:228316817-228316832 | TGAACTCCTGACCTC | - | 6.22 |
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| Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
SE_28342 | chr2:228314003-228317657 | Fetal_Intestine | SE_29240 | chr2:228314008-228317822 | Fetal_Intestine_Large | SE_35773 | chr2:228314622-228317736 | HepG2 |
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| Number: 1 | ID | Chromosome | Start | End |
GH02I227449 | chr2 | 228314135 | 228317575 |
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Enhancer Sequence | AGACACCCTT CTGAGTGCTT TCTAAACCCC ATTAACAGAA ATTAGTGTTA AAAGTTAAAA 60 ACCAGTAATA ATCTGACCTT CAAGCATGCT ATACTATAAA CTGAACTCTC TATTTTCTGG 120 CTACTGCATT TTCCACTACC AGCCCTAGCC CAGGTTGCTT CCTCTGCCTG AGATGTTCTT 180 TCCTCCCAGC GCCATGTGCA CTCCAAATCC TGCCCATCTT AACTGCTACT TCCTCCAAGA 240 AGTCTCCCTT CCCTTATCCT TCAAGACTGA GGGACTCATG CCTTCCTGTG AACTGCCTTA 300 GTGAATTATC TCACCCCTCT TGTGACACTT CACTTTCTGT CTTGTTTTAA GATCTTTTGT 360 GTTTCCTTTT TTATTCCATT TTATTATATA AAAGTCCTTT GTGGAAAGGA CTTGCACCTG 420 GTTCCTTGTT CCATTCCCCA CACCACATGG CTCGGGACTT TGTACACTGT TTAGCAGATA 480 ACAATTTAAA TGAATGACCC ATTAGATATC ATGTTGGTGT CTGATATTTG TTCTACCCAG 540 AGTGAGTCCA TCTGGAGGGT GAGATAATGT CGTTCAGCTC CTTTCCAACC CCATCAGCAG 600 TCCTAGGTGA AGAAAGGCAA AGGCCTGTTA TAGATCAACT CCCTGGACTA ATGTTGCAAT 660 CATTCTCTTT GCAAACATGT GTCAGCGTTT CTGCTTCCAT ATCTTTCTAC ATATCCGCAG 720 TGAACAAACT CCCTAAGAAA CACTGGCTTA TTGAAATGGG GCATGTTACT AAATACACAG 780 CATTCTTTTT ATCTCCCTTC TCTGCTGTAT AACACACCAA CCTCCACTTG CACATTCAGA 840 AATATAAAAA TGATTACATT ATGTAAATCC AACCCCTTTG TAGGGATCAC TGCCAGAGAG 900 ATGTTAAAAT GACATTACAC CTGACCTTTC TGAAAAGGAT AATGCTCCAG AAGTAAATTC 960 TTACAAATGA GGATGGACAA CACTTGGAGT TCTTTTTTTT TTTCTTTTTT TTTTTTCTTT 1020 GGAGTCTCAC TCTGTCACCC AGGCTTGAGT GCAATGGTGT AATCTTGGCT CACTGCAACC 1080 TCTGCCTCCT GGGTTCAAGT GATTGTCCTG CCTCAGCCTC CTGAGTAGCT GGGATTACAG 1140 GCGCCTGCCA CCATGCCCAG ATAATTTTTT CTATTTTTAG TAGAAATGAG GTTTCACCAT 1200 GTTGGCCAGG CTGGTCTTGA ACTCCTGACC TCAGGTGACC CACCTGCCTT GGCCACCCAA 1260 AGTGCTGGGA TTACAGGCAT GAGCCACCAT GCCTGGCCAA CATTCAGAGG TTTTTTTTTT 1320 TTTTCTTTTT TTTTTAAAGA AACCCCTATT GGCTTGTTAT 1360
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