| Tag | Content |
|---|
EnhancerAtlas ID | HS048-32435 |
Organism | Homo sapiens |
Tissue/cell | Fetal_small_intestine |
Coordinate | chr6:111496930-111498410 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HNF1A | MA0046.2 | chr6:111497494-111497509 | TTTTAATTATTAACC | - | 6.25 | | HNF1B | MA0153.2 | chr6:111497495-111497508 | TTTAATTATTAAC | - | 6.24 |
|
| | 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 |
| GH06I111175 | chr6 | 111497057 | 111499103 |
|
Enhancer Sequence | GTCTCACTAT TACTCAGGCC AGAATGCAGT GGTGTTATCA TAGCTGACTG CAGCCTGGAT 60
TCCTGGGTTC AAGCCGTCCT CCTGCCCCAG CTTCCTGAGT AGCTAGGACT ACAGGCATGT 120
GCCATCACAC CCAGCTAATT TCAGCTATTT TTTTTTTTTT TAAATAGAGA TGGGGTTTTG 180
CTATGTTGCC AGACTGGTCT CAAGCCATCC TCCTGCCTTG GCCACCCAAA GTGTTGGGAT 240
TACAGGTGTG AGCCACCACG TCTGGCCAAG GACCAGATTT TTAATATTCT TTTCCACAAT 300
GTATCTGGTA CACAGTAGTT GCTTAATATG TTGGCTAAAC AAAGAGTGGA GATTCAGTAA 360
AGGGTGATCA GAGTGAGGTG AGATTAATTT GGGAAAGCCT AGAAGTGATT CTTGAGCCTG 420
ATTTGAAGGT GGTGCTAGCT GTGGATTAGT AGAGGGAGAA GGGCATCTCA GAGAGAGGAT 480
TGCCAACATG CCTTAATTTT ATCAGATTCT AGAGTTCCTT ATGATTACCT CAGCATGTTG 540
CTAGACTAGC ATTATTATCC AAAATTTTAA TTATTAACCA ACTTTAATCT TACTTTCTAA 600
CAAATTGTTT GCTTTTACTA CTGATAGCCT TTTCAAAAAA CTTTAACTAG TTTTATTCCT 660
TACCATAATT GTTTCAAAGA ACATAATGAT ATGATCCTTT ATCTTCCTAA GAAATGTGCA 720
ATTATTTGGT TAAACTGTAA GATTATTTAA TCCATTATTC TTTTGACACA TGCATGGCCT 780
TACAGCTTAC AAACTGGGAT CACTAAAGGA ATACACTTAA TTTAAGTCTT TCTGTAGTCA 840
GAATATGATT TCTTGTTGTC TTGCACAATA CTGAGAACAG TGCAGTACAG GGCGAAGGTT 900
GGTCTACAGC CCTTAGGCCA GCAAAAACAG GCACAACTGC ACCTCTGTGC AAATGTTCCT 960
GACATAACCT TGGGGAAAAA ATATAAAATG CGGCCTTTTC TTTTACTACC TTGTTTGGTA 1020
AGTACCTGGA AAAACTCCAT GAAATAATTA GATTTCATAG TTAATTCTAA CTTTTTTAAA 1080
AAATGTTTCA TTGAGACTAG GTTTTTGGTT TGTTAATTGA ATCACTGTTG ATTTTACCCT 1140
TCCTGGCACC AACCTTTATT TCTGAGCTGT GGAGAGCACA GTTCTCACTC AGTGCTGTGT 1200
GCGTCACCTG AAATCCACAG AAAGAGGTGG CTGAACAAAA TCACTGATGA CCTTAATGGT 1260
TATTTTTCAC ATATTCAGAT TAAATTAAAA TACGTTTAGT GCTACATGCT TGACTTACTG 1320
AGTTTTTCCC TCTATTTTGG TTAATTTTTT TTTTTTTTGG TTAACTTTTA CTTGTAGAAA 1380
ATATGTTGAT GAACAAAAAC CCACTTATAC TATAAGATTT TATTCTACCA AGCACACAGT 1440
AACAATATTG AAAGCTGCTT TCCATCTTTT TCATCTTTAT 1480
|
