| Tag | Content |
|---|
EnhancerAtlas ID | HS180-34595 |
Organism | Homo sapiens |
Tissue/cell | Small_intestine |
Coordinate | chr3:142320300-142322840 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nr2f6(var.2) | MA0728.1 | chr3:142322404-142322419 | GAGCTCAAGAGTTCA | + | 6.19 |
|
| | 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 |
| GH03I142601 | chr3 | 142320427 | 142322853 |
|
Enhancer Sequence | AATACAAGTA ATATATCATT TCATCTTTAT AAACCATCCT GTGAGATAGG TGCAACAATT 60
ACTCATTTAT TTTTAATTTT TATTTTTTAA AAACAGGGTT TCAGTCTGTC ACCCAATCTG 120
GAGTGGAATG GCACAGTCAT AACTCACTGT AACCTTGAAC TCCTGGGCTC AAGCAGTCCT 180
CCCGCCTCAG CCTCCCAGGT GTGGACCAAC GTGCCCGGCT TATTAAAAAA AATTTTTTTA 240
TAGTGATAAG GTCTTGCTAT GTTGTCTAGG CTGATCTCAA ACTTTTAGCC TCAAGCAATC 300
CTCCCACCTC AGCTTCCCGA AGCCCTGAGA TTACAGGCAT GAACCACTGC ACCTGACCTA 360
CCCTCATTTT CTAGATGAGA AAATTGAGGC TTAGAGAGAT AGATAAAAGC ATTTATCTGA 420
GGTCATATAG TTTACAAGTG GCTGAGCTGA GATTTGACCC CAGGCCTATC TGACTTTATA 480
CACTGAGCGC TCAAATAACT TAATCAAATA TCTTAACAAA AATGCAAAGC TCTTTCTGAG 540
GTAACTCTAA CAGATGCTTA GAATAGCCAC AGGTTTCAGC TGGTGGAACC ACCAACATTC 600
TTTGAGCCAC ATTTAAAAAA ACCAAAACAA CAGTGGTAAA TCGTTCCGGT TTTTTTTTTT 660
TTTCATTCCA CTTAGTCTTT ATCTCCTTTT CTCTTGAAGC ATTCCTAGAG AAAGGGACAG 720
CAGCTTTTTC TCTGGGTACA CCATTAAAGC CACTTCTGAT CTGCTCCCAC CCTCTTTTGG 780
GGTGGAGCTG TGATTGGGGA GTGAGTTGGT GGTCATCCAG GGCGTGTCTG TGGAGTTGGC 840
AATGGGAAAC TGGGAAGCTC ACCTTGTGTA GGAGCCTAAG AACTCTGGAG TGACCAGGTA 900
TAAGGATTTC TTTCCCTGGG GTGTCAGGAT CCACTGCTGG AAGCTCCTGG AATATCTATG 960
GATCATGACT CTAATCTTAG GCCTTTGAAC TATGGCCATA AACCCCCAGG AAGAATCCAG 1020
GTGTGAACAC ATTCTCCCCC AATTTTTAAG ATTGGGGAGT TGTGAAGTCC CTGTGGACTA 1080
ATTGGAGGTG GGTGTGGATA CCTCAGGAAA GGCCCCAGGT CAAAGACAAA TAATTTAAAG 1140
GCCCCCCCCA CCCCATAGGC CCCAGCTTTG ACCTGTGAGA AAATGTGCTC CTCTCCCTCC 1200
TCTTGATGAA CCTAATTACA TAGAGAACTT ACTCTCCTGG GAGTCTCAAA ATGGAACTCA 1260
GCTGAGAGCG TGCTTCCCTC CCTTGCTGCC TGAGCTCTCT TTCCATTTCC TGGTTCTGCT 1320
TTACCTTCCC CTGAGTGGTT CTGTGTTCCC AGGATATGAA AGGCAGGGCC GCAGCTTCTG 1380
GCTTCACCGG GCTAATTTTT GTATTTTTAG TAGAGTCGGG GTTTCACCAT GTTGGCCAGG 1440
CTGGTCGCCA ACTCCTGACC TCAAGTGACT CGCCCGCCTC AGCCTCCCAA AGTGTTGAGG 1500
CTGAGGCCAC CTCTGGCCCT CATTCTCTCA ACATTCAAAA GCTTGTCACT TCATCCAGTT 1560
CCGAATTAAC ATTTTACTCT GGCTGATGAT GAACGTCGGG GAGAAAGAGA CATTTGTGCT 1620
GCATACGGGT TTATTGGTTA TAAAATGGTT ATACAATTTT GATTGCTGGA AACTTTGCTG 1680
ACATGTAAGG TCACATGAGA TGTGAGGCTG TTCAACTTTG ATCATCTGAT TTCTTTTTAG 1740
CACTGTGTCT GAAAGTGCCT ATGTGCCGTT TTTGGTGAGA CATATGTAGC ATGGCTTCTG 1800
TAAAGGCACG TTGCTTTTTA TTATAGTAAT ATTGTGGGCA CAGAAAGGGT GAGGAGTTAG 1860
ATGATTGGGA GAGTTTTTTC TTACTTAAAA CACTTGTTTC ATCAGAAAAT ATTTCCTAGC 1920
AGAGTTAGAC ATAGCTTTGT TCATAAAGTC CAGTGGTGAA GGGACTTCAG ACTTTACGAT 1980
AAACTAAATT TTATGATTGA CTTTTGTGAG CAATTCACAG CTATAAAACT ACGAGACTGG 2040
CTGGGCATGG TGGCTCACGC CTATAATCCC AGCACTTTGG GAGGCTGAGG CAGGTGGATC 2100
GCTTGAGCTC AAGAGTTCAA CACCAGCCTG GGCAACATGG CAAAACATCG TCTCTACAAA 2160
AAAATTATCT GGGCATGGTG GCGCGTGCCT GTAGTCCCAG TTACTTAGGC TGAGGTGGGA 2220
GGATCATTTT GAGCCCAGGA GATTGAGGCT GCAGTGACCT GAGATTGTGC CACTGCACTT 2280
TAGCCTGGGT GACAAAGTGA AACCCTGCCT CAAAAAAAAA AAAAAATACC TACAAGAACA 2340
TCTGGGTGAT AACTCACTGC ACACAGACAT GCCTCCTTCA AAAGATCCAA GCTGACCACA 2400
AAAAAAAAGG AGAAACTGTC TTTTCTTGAT AGTAAATTGG ATGGAGACAT TAGTAAGGTA 2460
GAAGGTGTCT GAGGGGCTTC TTCATGATAA AAAGCAAAAG GTTTTGGGGT GTCACTGACC 2520
CAAAATATTA GCAGAAATCA 2540
|
