| Tag | Content |
|---|
EnhancerAtlas ID | HS098-31333 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr2:121346940-121348780 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CDX2 | MA0465.1 | chr2:121348744-121348755 | TTTTATGGCTT | - | 6.62 |
|
| | 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 |
| GH02I120588 | chr2 | 121346373 | 121348934 |
|
Enhancer Sequence | CAAACACGTA AATCTAAGTT ACCACCCTGG TTAAAACCTT CTATAATTAA CACAACAACA 60
CAACCTGATT AAAAAATGGG GCAAAGGACT TAGGCATTTC TCCAAAGAAG ATATACAAAT 120
GGCCAGCAAG CACGTGAAAA GACACCCATC ACCCATCTTT AGGGAAACGC AAATCAAAAC 180
CACAATGAGA TACCATTTCA CACCCATTAA GATGGCTATT GCACAAATAT GGTCCATTGC 240
ATAAATATAT CTCTTCTCCT GTTGATGAAC GTCTGGGCTC TTTCCAGTTT GGAGCTATTA 300
TGAATAAAGC TGCTGTATAT TGGGAGACAA TTCCCCATGA GTCTCTCGCA TTTCTACACA 360
TCTTATGAGT AAGGCACTGA TTGACCTATC TTTTCATGGG TGTTTGTATT GCAGACAGCT 420
TTGGAAGATC AAGCGTCTCC CTCTGGAGCA AAGGGCAAGC ACGCTTGCTT CCCATTGTAA 480
AAGATCCAGG TTCCCTAAGC TCAGGGTTCC TCTCCTGTAA TGCAATTCAC TGCAAGTACA 540
GGATCCATCT GGGCCCACTC ACATTGTTCT GTGGGACTTG GGGCAAAAGG AACTGACGCA 600
AATATGCTGA TACACATGCT GTTTGCTGTG CTGTGAGGAA TAACATCCTT TGTCTCTGAC 660
TCATGGTTCT GGCATCTTCT GCCAGCCTCT CAAGAGCCTA ACTCATTACC TTTCAAGTTG 720
AGTAAAATTT CAGACCCTTT ATAGTTCTTG ACATTAAGTG TTCTTATACA AGTGTTTCTG 780
GGAACATATA TTTTCCCACT TCTTCTTTGT CCTTCTCATC CTGCTGCCTG GAGTGCGGAC 840
CTGATGGCTA GAGCCCTGGT TACCATCTTG ACCCATGAGG ACCAGAGACG TAGTGGGTAG 900
AAGGAGCATG GGTGTCCAAG GCTTTTGCAG GTCAGAGTGA TCATATTGGC CCTGGAATTT 960
TACAGGAGGG AAAATGCCTT GCTTACACCA CTGTACCGTG GTGTTTTCCA ACCCTATCTA 1020
ATGCAACCCA TGTCGTGGCT CATCCTGTCT GGGATGTTTT CCCGCCCTCC CTTCCTTTGT 1080
TCACTAATGT ATATCATACT AACCTCAAGA ATGACTCTTC ATATTTCTAG TTCTTCCCAC 1140
AATGATTGCT TCCTGTATCC TAGGGCCTTG TACAGTGTCT GGCACAGTAG TAGGTGCTCA 1200
GGAGGTAGGA GTTGATGAGG TGAACAAATA CATAAAAGAA AAACGCAGGT TGGCAGAGAT 1260
GATGGGAAAG CGGCATTCTC ACTCAGAGGA ACAGGTAGAG CATTAGGTTG TCGGGGAGGG 1320
AGCCCGAGCT ATAGTCCTGT ACCGGATGAC ACCACCGCAG CTCTTTCCTC TCTGGGCTCA 1380
GTTCTCTGGC TCTGCAGTGT GGGCTTTGGC TAGGATGATG AATGCCCATG GTCCCCACTG 1440
ATTCTCAAGC CCTGTGCAAA CTCTGAAATT TGAATACTGC TTTCCTGGCA ATGCCTCCCT 1500
GCTTTTCTCT CCTGTAACTT ATATTTGACC AGTGGCATCA CTTGATGGCT GAGAAAGGTC 1560
CTACTCCTTG CTGGGCCCAG GACTGCTCTG CAACCCAAGC TTGGGGAGAC ATGGGTGCCT 1620
GGGCAGCTTA GCAGCTGGGG AGACTGACAG CTTTAGTGAG CCCAGCGGGT GGCATCAAGT 1680
TTCTGGGTGC CTGGTCACCA TGTTAATCTG CTCTTGGTGC CACTAATACC AATTTGTGAG 1740
CAGACAGCCA GGATCAGACA GGCCAGCTGT CAGGCAACTG TGGACAGCTC AGTGTGTGGT 1800
TTGATTTTAT GGCTTAGGGC TGGAATTATA AATTAATTAG 1840
|
