| Tag | Content |
|---|
EnhancerAtlas ID | HS044-06892 |
Organism | Homo sapiens |
Tissue/cell | Fetal_kidney |
Coordinate | chr2:28303150-28304590 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| BCL6B | MA0731.1 | chr2:28304296-28304313 | TGCTTTCTGTGAATCAA | + | 6 |
|
| | 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 |
| GH02I028080 | chr2 | 28302898 | 28304815 |
|
Enhancer Sequence | ATACTCATTT AAAAATAACT GTACCATCCA GCATTTCAGA AAAAGCATTA AGGACATGTG 60
TTTCATTTCC TTAAATGAAA ACAGATTATA ATGTATGTAA TCAGAGCATT GAAAAGAGAA 120
GGAGAGAGAG GTGATTTCAG TACCAAAATT TGTCTATAGG ATAGACTACC TGGATGAGGC 180
AAAAGGATCT ATAGACTACC TGCCTCAAAA ATCTCTAGAT ATAATGAGAG AGATGGTAGG 240
TACTCCTTGA GATGAGATAC TAGTCTGATG ATGGCTTTTT TTGGTGATGG CTGTTGAACA 300
ACATGTAAAT AAAAGCAGTA ATCATGTTAG AAGAGACCAA TCTGTGCCTG TGTTCTGTAG 360
ACTACATTGT TAAGAGCATG GTTCAAATAT TTGAAAGAGA AAAGAAAACT GCTTTTAAAA 420
CCACTTACAA TTACCTTGGC ATTCTCATTT TAAGTAGCCA TCTGCAAGCA TATTAATTTT 480
ATTATTTCAG TGAACTCCCT ATTTGATTAA TCCGTGACCT GATTTAGTAA ACATTTGTCA 540
GGATATATCT TCCCTGGAGA TACATTAAGC TTGGAGCATG TAAGGCATCT TTTTTCCTAT 600
TCAAACAGTG AAGTTAGGAA AGTGTTGTGG TAATAATGTG AGCACAATTG TCTAAGAACA 660
TTAAGAACCT TCGTCTGGAT CTTTTGTTAC CATAAAAGGC AATGTATCAT GCTTTCCTGT 720
TTTGCATGGA TGAGAAGGGA GTAAAAAACA CCAAAAGAAT TTTTATTGCA TAGAAATATT 780
TCCTTCCTAG CAGTTGGTGA AGCAATAATG AGCCTACAAA ACAATCTTCC TATAGCTGGG 840
GAGAGGAGGG CAGGAAAACG TAGTGCAGCC AGCCACATAG ATTCGCAGAC TGGCAGGCTG 900
GTCACAGAGC GCCTGCTTCC ATCCAGAGTC CCTTCTACAT GTAACTCTCC CCAGGGCAAA 960
GCGCCTGCAT GTGCTTCTTC TCACAGCCCT TTAAGATATA CAGGGCAAGT AGGAGCTGCT 1020
TCTTTTCTAG AAGAAGAACT TATCCAAGCC TGTGGTGCAG ACGATTGTTG TAGGCAGGCT 1080
AGAGCCACAC TTACCTGATT CCCAATTTGT ACGTAAGACC AGGCAAGGTC CACTGTGTTG 1140
AGAAGATGCT TTCTGTGAAT CAAATTACTT GGTACAGAAA ATGTTGCTTT CAGTGTATCT 1200
TGTGGCAACT TTAACATTGT AGACATCACC ACTGAATAAG ATGAATGCGT GGGAATTGTG 1260
GATTTGAAAA CACTAAAAGT GGTTATCAGG CTTTAGCACA TCTTAAGAGT CTGCATTTCC 1320
ACTAGCCTAA TTCACACTGG GCCCTTCTCA GCGTTTCTTA ATGCTACGCT ACTCCCACTT 1380
CCTTTCCTCT GTTTCCCTCA CTTCAGCCCT AAATGAATTT AGGTTGTTGA ACAGAAATGA 1440
|
