| Tag | Content |
|---|
EnhancerAtlas ID | HS034-21627 |
Organism | Homo sapiens |
Tissue/cell | ECC-1 |
Coordinate | chr3:135995910-135997070 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZNF740 | MA0753.2 | chr3:135996446-135996459 | GTTGGGGGGGCGG | - | 6.27 |
|
| | 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 |
| GH03I136277 | chr3 | 135996476 | 135997168 |
|
Enhancer Sequence | AAGTCTCCCA GCAAGGGATA TACCAACACT AGTGCTGATG GGAGTGTCAG GTGAGTGAGG 60
TAGACTCTTT GAGGTTCCTT GGTTACAGAA AGCCTTAGTG TGCTGGCTTT CTCGAATGCT 120
GGTTATAATA GTAGTGAACT GGTCACGTGG ACAGATGCAG GACCTCCTGG TTAGCCAGGG 180
TTTTGCAGGC AATGATGATA GCTTAGGTCA TGCACTGGTT TTCTCCTTTC TGTTCACAGT 240
GTTATTCTAC CTAGAGATGC TGTAGTGGAC TGTGTTGGTT GGCATCCAGC CTGGAGGTAG 300
CGTTTACAAA AGGGCACCAG CTGCAGTAGT AGCAGTGGGA TTCGAGCTTG TCCTGTGTTG 360
CCCAGGAGGT ATTCTGGTTT CTCAGGTGAC AACGGGGTCC ATAAAGCTGC CAAAAGTTTC 420
TGTCCTTTGT ATTAAGTAAC CAGGGTGGGT GGAGGGGTAC AGCCAGGTGG GGGCTGGGTC 480
AGGTGGGTCT ACACTCTGTC TCTCCATGTG TGGGGAAAGC CGTGGCTCCT ATGAGGGTTG 540
GGGGGGCGGT TCTCAGGTCA TTAGGGTAAT GTTCCAGAGA GGAATATAAC TGCCTCTACT 600
GCACAGAAGA GATCGCACAG TGTGTGGGGA GTAACAGGTG GCACTAAGCC TCACCCAGAT 660
CCCACACGGT CGGAAAGGCA GATCTCACTC CCTCTGTGCT CTGCTAGCTG CACTGGGCTA 720
AGTTCCAGGC AGCCTAGGCT CAGAACTCAA ACCTGCCCCA GGCCATAAGC TTTCCCTGTG 780
GGAAAGCAGC TGTGGCTTTC AGGCCATGCT CCTCCCAGGC CACCTGCAGG GCCAGGCACC 840
TGGCTCCTGC ACTTGTGGCT GCAGTGCACT TCCCCCTGCC CCTGGGAGGT ATGGGTTCTG 900
GACAAAGGAG TTCATCCTCA CTCAGTGTTA TATCTTGAAA TGGGGAGATT CTTTCAACCT 960
GCGACCACTA CCTGAGCTTG TTGGCTGACT TCCCCAAGGT CCCCTGTGAG GTACAATAAA 1020
GAATGGCTTA CCTTGGTCTG CACTGGAGAC TGGGAATGCC TGCAAAGCAC TTCCCGCCAC 1080
TGTTTCTACT TTTATATTTC TTACTGCTCC CTAAATCAGT CCCAGCCCTG GGTAAGGTTA 1140
AGGCCTTCCC CCATGGCCTG 1160
|
