Tag | Content |
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EnhancerAtlas ID | HS042-27003 |
Organism | Homo sapiens |
Tissue/cell | Fetal_brain |
Coordinate | chr2:217400920-217402720 |
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) |
IRF1 | MA0050.2 | chr2:217402625-217402646 | CTTTTCTTTCTTTTTTTTTTT | + | 6.41 | IRF1 | MA0050.2 | chr2:217402610-217402631 | TTAGAGTTTCTCTTTCTTTTC | + | 6.61 |
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| Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
SE_01759 | chr2:217399552-217401178 | Aorta | SE_01759 | chr2:217401227-217402584 | Aorta | SE_49133 | chr2:217399482-217402661 | Right_Atrium |
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| Number: 1 | ID | Chromosome | Start | End |
GH02I216533 | chr2 | 217398291 | 217402415 |
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Enhancer Sequence | CCATGTTCTT TGCCCATCCA TCCACCAACA CATCAACTTT TAATTAATTC ATTTATTTAT 60 CTACACCTAG TCCCTGGAGC CAGACTGCCT GAGTTTGAAT CCTGGCTCTA CTAGCTCTGT 120 GACCATGGTT AAGTTACAGA ACCTCTCTGT GCCTTAGTTT CTTCTTCTGT AAGACAGGGA 180 TAACAGTAGA ATCTGCCTTA CAGGGTTGTG AGGATTAAAT TGGTTCATGT GTGCACACAC 240 ACACACATAA ATAAAATATC AAGTGCTTAA AACCACTCAT GGCATGTAGT AAGCATGATA 300 TAAGTGTGTA CTATTATTGT TATGTTTGAA GCATGTTTTA AGTAATAGTG TGTGCTGGAT 360 GCTCTGTTAG CATCTTTTTC TATGAAACAT AGCACTCTTC CCTACTGCCT TACAAGGTAG 420 GTGTTATGAG CCTGCTTTTC GTATGAAGAA ATGAAGGATT GAAGAGTTGA CATGCCTTTT 480 CTGAGATGTG CCATGGACTA GGCTGCAGAG GACAACCAGA CACATCAGCA GGGCCCAGGA 540 GGGAGAGGCT GGAAAGAGCG GGCAGATCAC TGCCTGCCCC TGTCACCTAA TAGCCAGCTC 600 ACATGGCTTC CCTGCTCTGC TATCTGGTTC TTGCTGCAAC CCAGACTCCT GCTGATGTCT 660 TGTCTTGAAC TGTGTAACCT GTCAACACAT GAGAATCATT TGCAGCGACT GGGGAGTGAC 720 GTGATTCAGG AGCAGGGGAG GGGAGCTCGT GGAGAACAGA AAACTGCTGC TCCATTTTGG 780 AGCTGCCTTT CAGCCTGGCC AAATGGGAAA CTTCCTGCTT AGAAACAGTC AGGACATTAA 840 TACTCAGATG AGTGAAGACA CACATGTCTC CACTAACATC CCAGGCGGAT CAGACTGATT 900 ATGCCGCACT GTAGTGCAAT TTCCTCTTGG TTTTTATTTC TTTGGCTCAA CATTGTGCAG 960 ATGGTAAGCT CTGCTCACTG AAAATATGGA AATGATAAAA TAGAAATATG AGACATTTGG 1020 ATATCACTTG AGCTGAAACT TGACACTGCA GGTCTGATTG AAAATCCAGC AGGCCTCTTT 1080 CAAGACCCTT TACTGTGGCT CCTCGTTTGC TTCAGGAGGC CCCTGACAAA CTTGCCCAGT 1140 TCTCCCTAAA TCCTGCTATT GTTAGCTCTG GCCTGGGCCA CCTGCTTTCT CCTCACCAGA 1200 GATATTCGGC CAGATGATCC TTACCATTAA AGTCCCAGGA TGTGTGTGCA TGAGCACACA 1260 CACACACACA CACACACCAC ATATGCACCA CACACATGCG TGCACATAAG TGCACACACC 1320 ACACATCACA TATGTGCACA CATACCACAC ACATGCACCA CACGTGTGCA CATATGCACA 1380 TGCCACACCT GTACATGCAC ACACTGCACG CACACACATG CATACACATA AGCATATACC 1440 ACATGCATAC CATACATCAC ACACCACACA CCATATACAT GCATGCACAT ACAAAATTAC 1500 ATGCATCACA CACCACACAC ATGCATGCAC ACATACCACA CATACATACA TCATACCTGC 1560 ATGTATGCAC ACACACACAC ACCACACATA CATCCCCACA CACAAACACA CATGCCTTTT 1620 AGGTGCTACC CAGGACTCCC CTTCTAGCTT TAAACTCTTC ATGGAGAACT TTCTGCTGTC 1680 CACTGAACCT TTAGAGTTTC TCTTTCTTTT CTTTCTTTTT TTTTTTTGAG ACTGAGTCTT 1740 GCTCTGCCAC CCAGGCTGGA GCACAGTGGT GTTATCTTGG CTCACTGCAA CCTCCGCCTC 1800
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