| Tag | Content |
|---|
EnhancerAtlas ID | HS050-11511 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr11:19824340-19825810 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NFKB1 | MA0105.4 | chr11:19825229-19825242 | GGGGGATTCCCCC | + | 6.17 | | NFKB1 | MA0105.4 | chr11:19825229-19825242 | GGGGGATTCCCCC | - | 6.2 | | TFAP2C | MA0524.2 | chr11:19825177-19825189 | TGCCCTGGGGCA | + | 6.44 | | TFAP2C | MA0524.2 | chr11:19825177-19825189 | TGCCCTGGGGCA | - | 7.22 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH11I019802 | chr11 | 19824428 | 19828061 |
|
Enhancer Sequence | GCAATTTGCA GGACCTCTGC TCTCCCACAC AAATCAGCCT TCTAGGAAAG CCTCAGATGC 60
ACAAATTTAG AATGTATTTT CTTTCCTAAG AAGCCATTAA CCCTAACTAG GAAAAACAGA 120
CAGAGGGGAG CAGCTGCTTC CTCTCTGTTA TAAACAGCCA TTTTGATCAC AGAGGCCTCC 180
TTTCCATTCC TTTCCAGGTT TGTCATGTTC TTGCACAGAG ACGGTTGTGT GTTCCAGGCT 240
GGGGTTTATT TTTACCAGCA ATACAGATGT TTCTGCTCTT GTGCAAAATT TCATTAAAGT 300
TCAACCAGTG GTTTGCTGTG GGAGGAGGCT GCCAAGGTTA ATATTTCTGC GATGTATTCC 360
CTTCTGTTCA TTCTTGGCAC CAAAATATTC CCAGGTGGGC AGGTTGTGCT GGTGCTGTAT 420
ATCAAAACTA AACAACAGAA TCACCAGTTT ATCTGTTGAA CTCAGGTGGA GTCTCTGATC 480
ACACAGAGCG CATCAGCTTT GTCTTGAAAA TGCAGGCAGG GAGATACTCC CTCTGGTGAG 540
TATCTGCTCA CCCTTTAATG CCCTTTAGCA GAGAACGCCT CACACTGCAG AGGTTACCTT 600
GGGGGCCAAG AAAGCATTTG GCAGCATGAA ATGCTACATC CTTCCACTTT CCCACTGAAA 660
TGGTGGGAGC AGAGCTTCAG ATATGTGTTC AAATCCTGTC TGTGGCTTAG GCAAGTTACT 720
TACCTCTGTA GAGTGTCAGT GTCTTCATCT GCAAAATGGA ATTAGTCATC CCTGCCTCAA 780
AGGATATTGT GAGGCTTCAT TGAGATGCTG CATATAATTA ATTGAGATAG AGCAGAATGC 840
CCTGGGGCAG GGAAGATGCT TGTGAGAGGA AACTGTTAAA TGAGCACTTG GGGGATTCCC 900
CCAATGGTAG AGGATAATGT ATAGTCCAGG GAAGCCCCTC ATTCTTCTCC CTGCTTTTGC 960
AATGGAAAAA TTCTGCATGC AGCAGAACCA GTTCTTCTAC CTGAGAGCTT GAAAAAGGCA 1020
AGTTAAAAGT AATAGCAATC TGACTTGTTT GACGTGTGTT TCCTCTGCCT CGCCCCATCT 1080
GTGGCTTATC GAATTGGAAA GTGGTCAAAC AAACATGGCC CTTGTCTAGG AACAATTGGC 1140
AAGGGTAGGG TAGAGCTTGA AAGGGGTGTG GCTAGGATTA AAGGTGAGAC AAAAGTGATA 1200
TGGTATAAGG TGATCTGTGG CCAATTTGCT TAATGACTTT TACTACTTAC TTTCTGAATC 1260
CAGGTCTACT CATTAGGTCA GTGAGAAGAG CCAGACCTCA TGCACTAAAG AGAGCAGGTG 1320
TGTGTGTATG TGTGTGTGTC CTTCAGGTCT CTGCAGATTT GTAGGGTCAT CTGGTTAAAA 1380
ATAGATAATG TTCATACTCG TTTTATAAGT CTCCATTGAA GAAGGGAATA TGGACAAAAT 1440
TATTCATTTT CAATTACAAC GTCACCAAAC 1470
|
