| Tag | Content |
|---|
EnhancerAtlas ID | HS050-65047 | Organism | Homo sapiens | Tissue/cell | Fetal_stomach | Coordinate | chr8:18775810-18777240 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| KLF5 | MA0599.1 | chr8:18777085-18777095 | GGGGCGGGGC | - | 6.02 |
| | | 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 |
| GH08I018917 | chr8 | 18775355 | 18777243 |
| Enhancer Sequence | AAAAACTCTG CTCAGATCTC AGATGTCACC TCTTCCAAGA AGCCTTCTCT CCATCCTGAC 60
TGAGGTACAA ATTCACAGCC TCCCAAAGCC TCTGTTCTTA CCTCTACTGT AGCAGGTATC 120
ATCCTGTGTC AGAATCATGT TATTACTTGC CTGTTTCTCC AACCAGACTT CACAGTCAGG 180
CTGTAGGCTT CATATTTCTA CCTCTAGCCC AGCAACTACA GGTATTCACT GAATGCGTGT 240
TGAAAAAGTA AATACTTCCA GGAATGTACT GAAGGAAGTT TTTAGCATCT GGTACTTGAC 300
ATACTAATAA ACAAAAAACT AGGCCTCTTG ATTCTTTGCC CAGGCCTGTT CCCAGTACAT 360
CAGCATTTCT CCAACTGTGT TCCAATAACA TCCATTCAGA AAATGTGAAT AATGTGTGGG 420
TTTCCAGCTA TGCAACACAG CTTCCAGTTC CACCAACCTG TCAAACTTCC ACCACCCTCA 480
AAGCCTCTCA CCCCACCTTT TTGGTCTTCT ACGTGGAGGG AGGGCACTGT ACCTGTACCG 540
TGCCCCTTTC CCTGGTTCCC ACCATTCAGT CGTCATTCAT AAGTGCCAGT TCAGACCCGG 600
GGAAGACTAT CTGGTCTTGC AATATTTTTA ATAATCCTCT AAAGCTTGGC TAAAGACCGC 660
CCTGAAACTC ACCAGGCTCT ACAATTTCCT TAATTCTCCT TTCTACAGAT TAAGGTTTTG 720
CCTCTTGGAT TCTTTTTTTT AAGCACTAGT CCCTATCTTC ATGATTTTCA AAGAATATCT 780
AGAGTGGATA TATAATTTAC CTGCAAATAT GCTCAGTTTC TTAGGATATT ATGCCTCAGA 840
GTTTAAATTC ATACAAAAGG AGCCAGGTGA TCTCTTCCGG GGCTTCAGCT TCTTCTAGCA 900
GTGTTTGTTC TACCCTTTCA AACAAGCTGA CTGTACTCCT TGATAGAGAA ACGCCAGCCA 960
GGAAGGAGTT TCGTATCTCT GCTTTATCTC AGAAATCTCT TAGCATTACC TCACACACCC 1020
TTAGAAAGGA GCCCCACCTT TCCTTTTTCT CTTTCTTTTT CACACACCAC ACAGTTATTG 1080
CCCCTGACCC GTGAGAACAG GATTGCTCAA GCAGCCATCC AAGGACTACC TGAATCGGGA 1140
TCATCCGAGA GCTCATTCAA TACTAGATTT CTGAGTCAAA CAGAATCAGA ATTACTGGAG 1200
TGAGGTTCAA GAATCTGAAT TTTTAACAAG CATGGAAAGC ATCCAAGGTG GAAACAGATC 1260
GTTGGCTTGC AAGGTGGGGC GGGGCAGGAC TGGGGCGGCC AGGATCCCCA GAAACTGTCA 1320
CCTGCAGCCC AAGACCACTG CTTTCCTTCA CTTCCCTGCG CAATACAAAG AGTGTAATTT 1380
TCTATGTGCG CCATTTGTAG GGACATGGAT GAAATTGGAA ATCATCATTC 1430
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