| Tag | Content |
|---|
EnhancerAtlas ID | HS180-37038 |
Organism | Homo sapiens |
Tissue/cell | Small_intestine |
Coordinate | chr4:100072600-100073960 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| GFI1 | MA0038.2 | chr4:100073715-100073727 | TGCTGTGATTTG | - | 6.52 | | Gfi1b | MA0483.1 | chr4:100073715-100073726 | TGCTGTGATTT | - | 6.62 | | MNX1 | MA0707.1 | chr4:100073056-100073066 | TTTAATTACC | - | 6.02 | | POU6F1 | MA0628.1 | chr4:100073322-100073332 | ATTAATTAAT | + | 6.02 | | POU6F1 | MA0628.1 | chr4:100073322-100073332 | ATTAATTAAT | - | 6.02 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 2 | ID | Chromosome | Start | End |
| GH04I099151 | chr4 | 100072805 | 100072890 | | GH04I099152 | chr4 | 100073341 | 100073490 |
|
Enhancer Sequence | TCTTCCAGTT CTAACTGTTG TTGTGGCCTA ATGCTAAAAT GTTTTATGTT GCAAGTTTAG 60
AGAAGCAATT CTTTCCTCCA GTATAATTTG ATTTTGTACT CTTGGCTTTT CTTGATATGT 120
CTAAATTTTC AATGTAATCA GAAAACTCAT GCTCTTCCCA AGAGTCACAT ATTCCCCCGC 180
TCTACTGATA ACCTTGAACA CACCTGTGTC TTGTTAAATT CAAGCACTTT TTTTCCCATC 240
AAGTTTGACT TCCAGACTAT CTAAGTGAGC TTCTCACAAG GAGAAGCAGT CATATTGCAG 300
AAGTTCTTTT TCGACTTTTT GGTAACTGAC TTAAGAAACA GGATTTCGTA TTCCTATGTC 360
TTTATTAGGT TTTCAACTGC TTTTAAAAAA CTTGGGATTT AAAAGGGCTA AAGTTTTTAC 420
ATCCATATGA CCTTCTGTAG GTTCTCTTTA AAGTCTTTTA ATTACCAATT TGGTTAAATG 480
AGTAACTATT ATTTTACAGT GACCTGTGCT TCTGTTTTTA TCAAATGTTT TAAGCCTTCA 540
TCATTTTTAA CAAACATCCT CACAATTAAA CCCTAAATGA AGTCTGACTA ATTGCTGGGG 600
ATTATTAAAG CTATCAAAAC TAATCAAACA AAGTTATAAA ATCTTTTTAC AGCTTCCAGT 660
CGGGTCATGG ACTTCATTAT CACCATCTCT AGCTCCCTTG TAAAAGGTTC TTATCAGGTA 720
CTATTAATTA ATACTGTGCT ATTAAGTTAC AGGGCTTTGA CTCCTTAGTA CACATATGTT 780
AGCTAAAGAA GGCACTGACT CATGCAAGTA TCTGACATCA AACTCAAGTT AACCAAAGCC 840
TTGTCTCTGG ACCTGGGCAA AGGCAACAGA GTAAACAGCT TTCATGAAAC ACAGGGACAG 900
GCCTGTATTA ATAACCATTA AGATTTATTT AATAATTTTG CCTTTACCTG AAATCATCCT 960
TATGTTTTGT TTTACCCCCA GAATTTGAAA CTATGAAATC CTGCCAGGCC CAGAGACTAT 1020
CACATGAGAT TGTAAAGGCT GGTTTTGAGG AGTAAAATTA ATTCAGACCC TCCAAATCAA 1080
GGATGGTACA CAGATTCCTA AATAGCTGAA CAAAATGCTG TGATTTGTAT AACTAATTGC 1140
TAAAAGCCCA GATTGCAGTA GGTTGATGCA TAGAATTTAT AGATAAGTCA ATTTCGTAAC 1200
TTTGCTTTTT GGCTTTTGGT TTTGGGATTT ATTTTGCTTA AAAGAGGTGT TAAGGTTAAT 1260
GAATGTCTAC TCACTTCCAT TCCCATCTGG CCTAGTGCAT TAGTTGGCTG TAAGTCTTTT 1320
GACTCTAAGT CCCCTAGCCA TAGAGTTTCC AGCAAGGGCC 1360
|
