Tag | Content |
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EnhancerAtlas ID | HS050-59165 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr6:84685860-84687230 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
PHOX2A | MA0713.1 | chr6:84686100-84686111 | TAATTAGATTA | - | 6.32 | PROP1 | MA0715.1 | chr6:84686100-84686111 | TAATTAGATTA | - | 6.14 | Phox2b | MA0681.1 | chr6:84686100-84686111 | TAATTAGATTA | - | 6.32 | RREB1 | MA0073.1 | chr6:84686790-84686810 | CGCCAAACCACTCACCCCCA | + | 6.22 | Stat4 | MA0518.1 | chr6:84686215-84686229 | CCATTTCCTGTAAA | - | 6.08 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr6 | 84685889 | 84686552 | chr6 | 84686626 | 84686930 |
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| Number: 1 | ID | Chromosome | Start | End |
GH06I083974 | chr6 | 84684027 | 84687734 |
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Enhancer Sequence | TGTTAACTAG GTAATTCTAA ATTTGCATCT CCAAAGATAT GAATCACGTG AAACAAGGTA 60 GAAAATGTAC AACTCAAAGG CACAGGATTA GATCTAAACA AAGACAAGTT TTGTTATGTA 120 AACTTTAAGC TATTGTCTTA CCCCTAGTTA AAGTTCCATT AGGAACTTTA GGTGCAGAGA 180 CAGATATGCC CTTACAAAAT GTAAATTTCC TTTAAAGGTG GTATTTTCAA CTTAGCTGCT 240 TAATTAGATT ACTGGCTTTA GGGTGGAGGC CTTTAAGGAA TGGGGCGAAG AAAGTATACA 300 GGATTTTCTT ATCTAAACAT TAAAAACAAA GAGTAGTCGT CCCCTATAGT AATGACCATT 360 TCCTGTAAAC TGCCCTCAAC CACCCCTAAC ATTGTAGCTC TCATGCAGCA TTACACACGC 420 CAAAGGCAAA TACTCTCACA GTACAAGGTG ATCTCTGGTA CTCCCAAAAG CCAAATAAAT 480 CAGGTAATGC GATACAAGAA AGCAGAGCTT TAGACCTGAG AAGAATCAGC ACATGACTGT 540 TGAAACTCCA CAGCAAATCA GAACAGCTCA AAAAGGGGTG AGTGGCACCT TAATTCTGAG 600 TTCTTTAAGG GGTCTGAGTC ATTAGAAGCC TTCTCTATTT TCTTTTCACT TGGTACTGAA 660 GATGGCAAAA GGAGAAGGAG ATGTTAGATA TGAGTTCTAA ATTTCTTTTC AAAGAATCAA 720 TATGTCAGTA TGTTCAATTC TTTGCCTTCT ACTTTTAAAC TTAACTTCCT CATAAAGCAA 780 TCTTTGTCGA TTACCTGCTC AACCCTGACT GATTTCAATC ACCTGTTCCA CCCCGACTCA 840 CTCCGTTTAC CTCCTCCACC CTGACTCATT CCGATGACCT GCTACCTGCT CCACCCTGAC 900 TCATTATCCA CCCTGCATAA CCATTTTTCC CGCCAAACCA CTCACCCCCA CCCCCTCACT 960 CTCTTTAAAT TAGCCAGTTG GAATTAGTTT ATCCTGTGCA GTCTAACCCT AGCCAATAGG 1020 GGAATGACAC AGCAGCAAGG GCCACGTGCG TCAGGGATAA GAACCCCTTC CCCTCCCTTG 1080 TCCAAGTGTG CGCTCACCAT TGCTCCACTC TTCTATAGAA GTACCTTGCC TCGCTGAGAA 1140 TTAAAAAGAA AATATTATAT TCAAGTGCTA TTTCTTTTGT GGCACCAAAA CTTTATAACA 1200 GACAAATAGA GTAGAAGAAA AGTAAATGAG AGGACAATTT TTAAAGAAAG GAAGTGAACA 1260 GAGAAACCAA ATGCGTGCCT TTTTTTTTTT TTTTTTTTTT TTTTTTTTGC AGCTGCATGG 1320 AATTTTAGTG AATCCAGAGG CCTTGTTCCC CGTAATTTGG AGTTCTCCTT 1370
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