| Tag | Content |
|---|
EnhancerAtlas ID | HS095-28597 |
Organism | Homo sapiens |
Tissue/cell | HMEC |
Coordinate | chr7:127850960-127852420 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| STAT3 | MA0144.2 | chr7:127851889-127851900 | CTTCCCAGAAG | - | 6.14 | | ZNF263 | MA0528.1 | chr7:127851188-127851209 | GAGGGAGGGAGGAGATGAAGA | + | 7.06 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr7 | 127852317 | 127852400 | | chr7 | 127851810 | 127852021 |
|
Enhancer Sequence | GCTGGATGCT AATCTCAGGT CCCACCTGCA CTAGCTGTGT GGTCTCGGGA GAGTCTTACG 60
GGTGGGAAGG ACCAGGGCCT TGTGGGCTGA GAGGCTTGGG GAAGCCAGGG GGAGCCAGGT 120
CCCCTCACTG CTCTCGAAGA ACCGGCAGTG GTGTTGGAAC TCCCAGAGCT GGAGAGGCTC 180
AGGCCGGGAA GGGCTGTCCT GACCTGCGGG CCATCATGGC CTTTCGGGGA GGGAGGGAGG 240
AGATGAAGAG GTGGCACAGA ATTGACAAAG GAAAGGCAGG AATGAAAAGG AAGGTGGGGG 300
AATGTGGAAG GCAAAATGAG AAGTCTCTCC GGGTGGCTGA TGTCACCCTT TCTGATTGCT 360
CGAGGTGCCA GCAGGGGCAC CTTGGCAAGG TGTCCCCTCT CCCAGGAGGC TGAGACCAGG 420
ATCTGATCCA AGCTGGGCCA CCTGGAGAGA GTGGCCTGAA CTAGTCTCCA TCATGCTCTG 480
GGCCTGGGTT TCTGCATTTG TAAAATGAGA GGAATGTGCT GGATCAGATA CAATCTCCTC 540
TCCCACCAGG CCCACCCCAC ACTCGGCAGG AAAGCAAGGA CTGGGGCCCC AACAGCTGTC 600
CTTGAGAGTG GGAGCCGCTG AGGGCACAGG AAGGAGTTTT GGGGGCGGCA GGCAGGGAAG 660
CAAGCAGGAT GGGAACGCCA GGCTCTCAGG GGAAGGAACC AGATAAATCA TCAGCAAGGA 720
AAACCTATAG GTTTCCCCAA AGTACAATTT GAATAGAAAT GTCAAATGCA CCTGGAGTTA 780
TTACACCCTG TAATCCTAAT GACATATAAT CCTATACACC AACAGGATAA TATCACGAGT 840
GTGTGTGGCA ACACTGCCGC ATGTTAATCC TGCCTGCCTC CTGGGATGAT CTTTCTCATC 900
CCAGCAGAGC CTACAGAGCC TCCTTTGTTC TTCCCAGAAG TGGCCTCATC GGGCTGGACC 960
TGGGGGAGGT GACCAAGGAA GTGAAAATCA AAGAGCCCAA GGAATGAAGC TGGCATGGCG 1020
CTAGTCAGGG GATGGACAGG TGTGGTTTGG TGCTTTCATT TTTTGCCTAA TCTGGATGCA 1080
TCCTAAGTCC CCTGGAAGTT GCCAGCCCCA CATCAGCATC TGTGTTGAGG ACCCTCTTCT 1140
CTCCCCGCCT ACCCCCGCCC CTAACCCTTT CCTTCTCTCT CATTCTTCCT TTCCTGTATC 1200
CTTCCCTTTC TTCCCCAGCA TCTATGCTCT GTTCTGCCAG GAGCACTCTC GGAGATATGG 1260
TTCGTCCTCT TGAGAGGGAA AGCCTCCTGG GACTCGCGTG CACCCGTCCT GTCCAGCTGC 1320
GCTCCTTAGT TGCGGGCCCT GGAGCCAGGG AAGGTGGGAG TGGACTTTCG CCTGAGGCAG 1380
CAGCTGCGTG GTTAGTGGTC TGTGGCCAGG GGGGCATTTC AAGGTAGGGC ACAGAACTTC 1440
CAGGCCAGTG CACCAGCCCA 1460
|
