| Tag | Content |
|---|
EnhancerAtlas ID | HS148-10694 |
Organism | Homo sapiens |
Tissue/cell | NHLF |
Coordinate | chr2:225733990-225735500 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| MEF2C | MA0497.1 | chr2:225734163-225734178 | AGTTTAAAAATAGAT | + | 6 | | PHOX2A | MA0713.1 | chr2:225734796-225734807 | TAATTGAATTA | - | 6.14 | | Phox2b | MA0681.1 | chr2:225734796-225734807 | TAATTGAATTA | - | 6.14 | | Sox6 | MA0515.1 | chr2:225734224-225734234 | AAAACAATGG | - | 6.02 |
|
| | 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 |
| GH02I224868 | chr2 | 225733693 | 225736342 |
|
Enhancer Sequence | TTCAATTTAC TGACTAAAAA ATTACATGCT GTCAAACATT GTTTTCTCAT CATGAGGATG 60
TTATTTCAGG GAGTCTTCAG AATCTCATTC ATTAAATGCA GTAGTTGGCT CCTAAGCAGC 120
TTGGAGAAAT ATTTCAATTA ATTTAAAACA TGCTCATTGA ATTAAGAACA ATGAGTTTAA 180
AAATAGATTC ATTAATGAAA GAGTGTCAGT GAATAAATAA ACACTGATTT TTAAAAAACA 240
ATGGTATTAA ATAACAAACT GCTGTGAAGG TGAGGCTGAC ATTATTTTTT GTGTTATTGC 300
TTATAGGCAC AATGAAATTA TTTTTCTAAA GTAATTTCCT AGTTTTTCAA CATATGTATC 360
AACTGTAAAA TGAAAAACAA CACTGACGTA CAAAACACTC CAAATCAACT TAACCCTTTG 420
GCCTGACAGA TACCAAAGGA CACACTAACT TGGTTCTCTG TACTTGGCTG TGTTCTCTTG 480
CCTGGGGAGA TTGGCCCAAA TACAAACATT TGGCTTCTGA ATATGGGTCT TAGTACAAAG 540
AAAGGAATTC ACGTGGAAGG AGTCATATGC CCCTGGCAGT AGAAAGAAAA GCCCACTATC 600
TTTGATTTTC AGTTTCTAAA TTGCATTTTA AATTACATTT AAATATGTTC TGGGTCAAAA 660
AAAGCATCTA TTTTTATTTA ACAAGGTGAC TAAGTGACAT TACCATTTGA GGTAATGATA 720
TGATTTGGCT GTGTCACCAC CCAAATCTCA TCTTAAATTG TAGTTCTCAT AATCCTCACA 780
TGTCATAGGA GGGACCCAGT GGGAAGTAAT TGAATTATGG GGGCAGTTAC CCTCATGCTG 840
TTCTCATGAT AGTGAGTGAG TTCTCATAAT ATCTGATGGT TTTATAAGGG GCTTTTCCCC 900
CTTTTGCTTG GCATTTCCCT TTGCTGCCGC CATGTGAAGA AGGACATGTT TGATTCCCCT 960
TCCATGATGA TTGTAAGTTT CTTGAGGCCT CACCAGTCAT GCTGAACTGT GAGTCAATTA 1020
AACCTCCTTC CTTTATAAAT TACAGTCTTG GGTATGTCTT TCTTAGCAGC ATGAGAACAG 1080
ACTAATACAG GTATTTCCAA ATGGTTTCAA GGACTAAGTT TCTAGATTTT TGTTTTGTTT 1140
TTATTTTAAA ATCCTGCCTG AAAGCATGAT CAGATTACTC CTAACACTTT GCATTCCATG 1200
GGAGCTGCTC TTGCCATAGT CATCAACATC CTCCACTTTG CCATGTCTAC CAGATGGACT 1260
CCTCTTTCAC TTCATGTTCC TCAGCTTCTT GGCACCAATC CCATAGCTAC CCATTTGCTC 1320
TTGGTTTCAT GATACAGTAT TCCTTGGTTT ATCTTTATCC CAACAGCCAT CCCTGTTTAG 1380
TCTTCTTTGG TCACTTCTCT ATTCATTCTT CAGATATTTT ATTTGGTTCC TGGCCCCTTC 1440
TCTATGGTCA TAGATATTTT TAGATCCCGC CCCTCTCCCC CCAACCAACA TCATTGTCTG 1500
AACTAGACTT 1510
|
