| Tag | Content |
|---|
EnhancerAtlas ID | HS048-02859 |
Organism | Homo sapiens |
Tissue/cell | Fetal_small_intestine |
Coordinate | chr1:180494610-180497140 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Gfi1b | MA0483.1 | chr1:180495398-180495409 | TGCTGAGATTT | - | 6.32 | | IRF1 | MA0050.2 | chr1:180496326-180496347 | AAAAAAAAAAAGAAAGAAAGG | - | 6.1 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr1 | 180496093 | 180496482 | | chr1 | 180496538 | 180496703 |
|
Enhancer Sequence | ACTAATTAGA ACGTGCTAGA GCTACTCCAG GTGAGTCACT TAACTTACTC AGTAAGGGAT 60
AAACTGCTGT TAGGCAAAGG ACCTGAGAAA GGCTTCTTAC CAACTTTCAG CTCTGGGTTG 120
ATTCGTTCAA CAACTAATGG TATTTCCTGA TTTCTTCTTC CTGTTTCAGT TACGAATGTA 180
ATTGTAACCT GGATGTTACC AAGTCCAGTT TGCTTCTGAG GCCTCCTGCC TTTGCTATTC 240
ATTGTGGAAA CACCGTTGCC CTTTAATGCA TCCATCATCT CTGGCTCTGG AATCCTGCTT 300
CCTGCTCAAT CCTTGCTGCT TGCTCTTTCC TCCCTCTCGA GGTAGCCAAA GCAGACACAG 360
CCTGTCTCCT CTCTGTTGCA GAGCACCACT AATACAGAGC AGTTGCATGA AACAGATTTT 420
TCTGAAGATG TCATAACTAA TGAGAACAGA CAGAGCTATT ATAGCCTGGG GTAGGAAATA 480
ATTTCAAATA CAACATCAGA GATGATTGTT TCTAGAAATG CATTGGCCAT TCCCTCCATG 540
AGGAATTTCT TTCTATCTGT GTCCCTCCTT GGCACCCCCA GGCACTCCAA TGCCAGAATT 600
GCCTAAAAAG AGATCAAGAA ATATCCTTCC GTATGGATGG AACTACCATG TATTACATGC 660
CAGGGACTGA CTGCACTAAC AGTCTGATTC TCTCACTTAA TCCTCTCAGC AGTGTTCTGT 720
GGTATACATT CCTATTTTAC AGATGAGGAA ACTGAGTCTC AGAGATGGTA ACCTGGCCAG 780
GAACCCACTG CTGAGATTTG CATCCAGTTC CTTCTACCCC ACACCCATGC TCCTCACTGC 840
AACACTTGCT GTCTCCCTGT GTAGTCCTAG TCTTCGCATA CCCTCAGGTC ATCAGAATTT 900
AAATCTATTA CTTTACCCCT TAACTCAGCA AAGCTTTCTG TAGAGTCAGG TAAAATTTTT 960
CCCTAACATT TTCTTCCATG CAATTGAATC CCTTCTCCAA GAGCTCCCTT GCAAAAACGG 1020
CCCTCCCTCT CCCGAGATAA GTTTCATATT CACTCTGATT TCCTTTGCGC TGAAGTGTTT 1080
CTCCTCACTT ACACTTCTAG ATAACTTTCT GCTGTCTCTG CTTCCCCCAC TGCCCTTTTC 1140
GCTGCTTTGT CAGCTCCTCT AAGGAAAGAG CCTCATTTAA TGCCAGGAAC TAGGATCCAT 1200
TTGCCTCCCT CCCCTCTTGA AGCAAGGGAA TCAATCCCCA TAGATAAGGC AACAGGACGG 1260
TGGACTCTGC ACTGAATTTC TCAGGTGCCT TTTTCAGTGG TGTGGGAGAG AAGGGGGACC 1320
CCTCCCAACC CGAAGCCATA TTTTCTTCCT GAGCTTGGCA CTCCATTAAG CCAGGACTTT 1380
CAGCCCACCT GAATCCTCAT AATTCTTAAC TATGTCCTTG CCCCTGGTTG GGATAACAGC 1440
CACAGATAAA AGGGAGCGGA CATTCAAATG GAGTTATAAA GTACACACCG TGGTTCTCCT 1500
CCCTGACCTT GCTCTATACA CTGTCACAAA ACAAATCCAC AGTCCCACAG AGACCTTAAC 1560
CCAGAGGATG GTGAGAAGCA ACCCAAACTA ATATATAGCC CTGTCTCTAA GTACCAAGAG 1620
ATGACAATGA CAGCAGTTGG TTACATGAAG GCATGAACCA ATCAATGGGT TTTTTGAGAA 1680
CCAATTTGGT AGGAGGCATG CTATCAGAGA CGTTAAAAAA AAAAAAAGAA AGAAAGGCTG 1740
AAAGATAAGC TGCACTGATG GAATTTACAG CCTGTTTCCA AAGATAGGAT AGAAAAGAAT 1800
AATTATCCGT TCCGGAGATG ATATGCCAAG TTATAAATGT GTTAGGTAGA CAGCAAGGGC 1860
TCCGGGAGTT CAGAGAGGGG AGGCAGCACT GACCTGGGAA AGGACAAGGA GACTTTCACT 1920
GAGAAGAGAT AAGGCTTGTG CATAGACTTC TTCAGTAGGC CAGAGGGGGA AGGACATACA 1980
GAGTCTGGTG TGGAGAATGG CATGAGCAAA GGTGCGGGGA CAGGAATGTG AATGGTGTAT 2040
TCAAGGGACA ATGACTCATT CACTTGGCTT TCTTTACAGC TGCCACATAA TAGTGGACAC 2100
ATAACTGATT ATTATTATTT TCTGTTTTTA AAGACCTCAA GAATAAAGCA AGAGACTCAG 2160
ACTCTCAATT TAGTGCTCAG TGACCCCAGT GCTCAGTGAC CCTGAGGAGG TCAAGGTGAA 2220
TCCGAGCCCT GTCAAAATTC TCACCCTCAT TTGCTGGAAA CTCCATTGAT TTAATGCTGT 2280
GGTTCAGGAG TCTAATCTTT GGAAAACCTA AAAAATAACC TGGTCAAATC TTAATTACTA 2340
AGCATAGCAT CATTTATGAT TTTGACTTTG TCAGAATTGG TCACTAACTT TCCCCGTTTT 2400
AAAACACTTC AGAGCTATTT GGAGCCAGGA AATATCTCTA CGAGGAGGCT AATCCTGTTA 2460
GGAAACACTG TTGTCCTCTT TTTTTTTTTT CTTGAGACGG ACTCTCACTT TGTTGTCTAG 2520
GCTGGAGTGC 2530
|
