| Tag | Content |
|---|
EnhancerAtlas ID | HS048-03667 |
Organism | Homo sapiens |
Tissue/cell | Fetal_small_intestine |
Coordinate | chr1:230842780-230845470 |
SNPs | | Number: 2 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZNF263 | MA0528.1 | chr1:230843972-230843993 | TATTCTTCCTCCTCTTCCTCC | - | 6.98 |
|
| | 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 |
| GH01I230707 | chr1 | 230843691 | 230845900 |
|
Enhancer Sequence | TACTGGGGAG ACTCACACAA CCTCGTTGTG ATGAATGGAT TTGCACACTG GGCCTTGGGG 60
GCAGGGGTGA GCCCTCTGTT TCCCCTCCTG CTCACAGGGC CGTGCAGATG ACAGAGAACT 120
CGGGAGAGCC CGTTGTGGGA GAAGGACACA AATTTGTGTG TGACGCAGTT ACCTGGGGTC 180
TTTCCATGAC AGCAGCCCAC CCTCTGCCTC GACCTTACAC TAGCACATCC CTGCCCTCGG 240
CTGTCCTCCC ACTCATCCTG AAAGGCCTAT TCTGCGGTTG TTCTTAGGAG AATAGGGTGA 300
AGTTGTGTAT AAGTTTGTCA CAGAACAGTC CCCTGGGCAC GTGGCACTTG GGAGTCTGAG 360
TAGAGATGGT TCAGAAACAG TGAGGTCTCC CTTTGTACTG AATTGGAGGT CCCAGCATGA 420
AAGTAGGGCA GCTGGGAGGA CAGAACTGGC AGGCAGGAGC TGGGCATGGC TGTGCCTCCC 480
CTGGGTCCGG GTCTCGTAAG AAGGCAGTGG CAGACCTGGC ATATTTCTCG TCCTCAGTCC 540
TCGGAGCACT CAGTCTCGGA AGGGCATGTG AGCGGGAAAC TGCAGGGTTC CCCTTGCACG 600
TTCCCTGCAG GGACCTCGGT GCTGCCCACC TGGGCTGGCA AGGCTTTTAG TTTAGAGGGG 660
GGAAAGGGAC AATTCTTTTC TTCCAACAAA CTAAACTAAA AAAGGGAAGC TGCCTCCCAA 720
AAGACGCTGG GATTTGACAT GAGAGTGGCT GCCGTCTTCC CTCTGCTCGT CTGACATGCA 780
CAGCTCACCA TTCTCATCCG GAGGCTAGGT AAATCTGTCG AGGTCAAGTC AGGACCTGGT 840
GTCATGGAAA CCACCAGGGC CAGCGCCCCA TGCTCAGGAG CACAGCAAGC ACTGGGCAGA 900
CGGTACCCTG GAGCCCATCA GGCCCCAGAT CCTCAGGTCC TCTCTAGTGG GACACATCTA 960
GCTGCCTGCT GAGGTCATGT AAATAGAACA TCATTGCTAA AGGGAAACCT AGAGGTCCCG 1020
AGACAGCCCC CGATCTCCTC ACTGGACAGA CCATGTGGGC AGGAAGTGGC TGCCTCCTTT 1080
GACGGAAACT GAGGCCAGCA AAGTTAGGAA GTGGGGCAGG GTCAGGGCAG CATGCGGTGG 1140
AGGCCGGCGA GGATCCTGGG CTTCCTTTGA GTCCCGATGT GGTTGGCTTT TTTATTCTTC 1200
CTCCTCTTCC TCCTGGCCTG GCTCTGCGGT CTGGGTCAGG TGGATGTGCT CTCTTTCGAA 1260
GGGAGACCCA TTTCAGATGC CACTGGCTTT CTTGCCTTTG CCTTCTGCAG GACCCTCCTT 1320
CTCAGTGAGC GCTCCTCCCA GCACTTCTCC TAGGGACAGC AGGCTAAGTC CATGTGTCCC 1380
TGCTCTGCCC TGCACAGTGT GCTGCCACCC TCAACCGGGC AACCCTCGGG CTGGCCTCTG 1440
CCCCTGTGAC CAGTCAGTGC CAGGGCTGAG CAATCCCCCC ATCTATCACC TCTCCCTGAA 1500
CCCGAAGGGA AAGACCTCAA GGAGGTTGTT GTGGTAAGAA AAATCACTAT GCGCCACTGA 1560
ACCTCTTTCT CCACAGTCTT GTCTTTCACC TCCCGCCTGG CTCTCTGTCC CTCACGAGGT 1620
TAACATCTTG ACAGAGCCTC CTCAGTGTCT CTTAGACACA CCCCTCAGCC CCACCCCACC 1680
CATGGATTTG CCGAGCTGCT CCCTGAGCAC GTGTTCCCGT GACTGTGTGC CTGGACTCTT 1740
GCGTAACCTT CAAACAATCC TCCCTGCCTC CAGTCTGCAC ACGGCAGGCT TCCGGGATGA 1800
CCTCTGAACA GAACGCGTCC CCATTCCCAC ACCTACCAAG CATGGCGTTC AAAGTGTCTC 1860
CAGCTCTGCC CTCCCCAGGC CCATTTTCTG GTTCAACACT CATGCCAAGC CAACCGCCCC 1920
ATCCTCGTTC CTTGCCCCAA ACTCTGCAGG CTGGGCTCAT CATGCTTGCT CCTAGCTTCA 1980
CCAGCCCTGT TGCCCTCACT GCCAGGCAAG GCCTGCTCTC CGCTCCCCAG TGACCTCTGT 2040
CCTCTGAGAG CCCCGAGGCT TCCCTGAGTT ACCTTGTGGA GCACGTTTCC CTGCAGCTCC 2100
AAATCCTAGG CATTTGCCCA TTGACCTTTA AAAGCCTGGA GGCAGGGCCT ATACAGCCCT 2160
CCTCTGGCCT CCTCTGAGAT GCCAGGCTTA AAGTCTTACA AGTAGCAAAT CCTCAACAAG 2220
TATTTGTTAA ATGAATGCTT TAAGCAATCT GTGGCTGGGT GCAGTGGCTC ACACCTTTAA 2280
TCCCAACACT TTGGAAGGCA GAGGTGGGAG GATCGCTTGA GGCCAGGAGT TCAAGGCTAC 2340
AGTGAGCAAT GATGGCACCA CTACACTGCA GCCTGGGTGA CAGAACAAGA CCCTGTCTCA 2400
ATAAAAAAAA AAAAAAAAAT CAACAATCTT TGTAGTAGAG GGTTTTCAGT AATGCCCCTC 2460
CTAACATGAA AGGGATTTAA GCAAGCCAAT TGCTTATTTC TGCATGGGCC AGGGACCCCA 2520
GTTCCTGACC TTCTCAAGAG ATATGAACCT GACCCTTCTG AGTGTAGAAC TGGGCTGTGG 2580
GGCCAGGAGA TGTGGGTTTC AATCCCAGGA CCCCCACTGG TGGCTGTGCC ATCTTGAGCA 2640
AGGCACTTTG TTTCTCCGAG TCTCTATTTC TTCACTGGTA AACAAAGGCA 2690
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