| Tag | Content |
|---|
EnhancerAtlas ID | HS180-21678 |
Organism | Homo sapiens |
Tissue/cell | Small_intestine |
Coordinate | chr17:73603080-73604140 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HNF1A | MA0046.2 | chr17:73603500-73603515 | GGTTAATAATTAATT | + | 6.01 | | HNF1A | MA0046.2 | chr17:73603500-73603515 | GGTTAATAATTAATT | - | 7.28 | | HNF1B | MA0153.2 | chr17:73603501-73603514 | GTTAATAATTAAT | + | 6.98 | | Lhx3 | MA0135.1 | chr17:73603506-73603519 | TAATTAATTATTA | + | 6.18 | | Lhx3 | MA0135.1 | chr17:73603503-73603516 | TAATAATTAATTA | - | 6.18 |
|
| | Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
| SE_23082 | chr17:73602792-73603500 | Colon_Crypt_1 | | SE_24179 | chr17:73602895-73603360 | Colon_Crypt_2 | | SE_27754 | chr17:73602695-73603710 | Fetal_Intestine | | SE_52698 | chr17:73602596-73603512 | Small_Intestine |
|
| | 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 |
| GH17I075606 | chr17 | 73602736 | 73603990 |
|
Enhancer Sequence | GCTGGTGACA GAGCTGGGGA TGCCAGAGAC GGGGCCTCCC AGGCTGGTTG GGAAGTCAGA 60
TTCAGATGGT AGAGCAGCCA GTGATCTTCC CAGAGAGTAA CTCGAGGGCT GAGAATGAAG 120
TGAAGACAGT GCAGAACATC GGGGGAGCCA GGCATCTCCA CTATCTATTT CCAACACGTT 180
TTCATCCCGC AAACAGAAAC TCTGGACCCA TTAAGCAGTA ACTATTGCCC CCAAGACCCC 240
CAGCCCCTGG TAACTTTCAG TCTACTTGAG TCTCTATGAA GTTGCCCATT CTAGATACTT 300
CCTGTAAGTT GACTCATACA ATATTTCCTT TTACGACTGG CTTCTTTCAC TTAACATAAT 360
GTTTCAAAGT TCATCCATGT TGTAGCATGT GTCAGAAATT CATTCAGTTC CAGGCTTGAG 420
GGTTAATAAT TAATTATTAT TATTATTATT ATTATTATTA TTATTATTTG AGATGGAGTC 480
TTGCTCTGTT GCCCAGGCTG GAATGCAGTG GCTCGATCTC GGCTCACTGC AACCTCTGCC 540
TGCCAGGTTC AAGCAATTCT CCTGCCTCAG TCTCCTGAGT AACTGGGATT ACAGGCACCC 600
ACCACCCGCC ACCACGCCCG GCTAATTTTT CATATTTTCA GTAGAGACGG GGTTTCACCA 660
TGTTGGCCAG GCTGGTCTTG AACTCCTGTC TTCTGAGTCG ATCCACCCGC CTCAGCCTCT 720
CAAAGTGCTG GGATTACAGG CGTGAGCCAC TGCACCCGGC CTGTTCTAGT CTGTTTACAA 780
ATCTTTGGGG TATAGGCCAA GGAGTGAAAG TGCTGGTAAT TCTATCATAT GGTAATTCTA 840
TGTTTAACTT TCTGAGGAGC TGCCAAATTG CTTTCCATAG TGGCTGCATC ATTTTATGTT 900
TCTACCAGCA ATGTACAAGG GTTCCAGTTT CTCTACATCC TTGCCAGTAC TTATTCTTTT 960
CCATTTTTAA AATCATAGCC CTGCTAGTGG GTGTGAAGTG GCATCTCATT ATGGCTTTGA 1020
TGTGCATTTC TCTAGGACTA ATGACGTTGA GCATCTCAGA 1060
|
