| Tag | Content |
|---|
EnhancerAtlas ID | HS136-16569 |
Organism | Homo sapiens |
Tissue/cell | Monocyte |
Coordinate | chr6:12241060-12243230 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF1 | MA0050.2 | chr6:12241389-12241410 | TCTTTCTTTCTTTTTTTTTTT | + | 6.25 | | Mecom | MA0029.1 | chr6:12241087-12241101 | CTTTATCTTGTCTC | - | 6.11 | | Nr2f6(var.2) | MA0728.1 | chr6:12241622-12241637 | TGAACTCCTGACCTC | - | 6.22 | | POU2F2 | MA0507.1 | chr6:12242781-12242794 | ACATGCAAATGTG | - | 6 |
|
| | Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
| SE_27736 | chr6:12240386-12243434 | Fetal_Intestine | | SE_28655 | chr6:12240476-12243477 | Fetal_Intestine_Large | | SE_34057 | chr6:12241746-12243025 | HCC1954 |
|
| | 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 |
| GH06I012241 | chr6 | 12241517 | 12243184 |
|
Enhancer Sequence | AATTGTCTTT AATGGGAGAT CATGTGGCTT TATCTTGTCT CTTTTTTGCA TCCTGCTGCC 60
TGGAACACAG ATGTGATGGC TGGTGTTGAT CCTGCTGTGT GCTGAGGGAG ATGGAACATC 120
AAGGTAGAAA GCACTGGACC TTCTAAGCAT GGTGGAGCCA TTATGCCAGC CCTGGATCAT 180
TTACATTCAG ATGAGTGTGC AAATTTTTAT TCCCTTAAAG CCACTTAGAT TTTGAATTTT 240
CAGTCACTCT CAGCTGAACC CAATCCTTAC TGCTCTTGGA AGACATTTAC ACTGTGGGAA 300
CCTTAGGATG CACTTTTTTT TCTTTTCTTT CTTTCTTTCT TTTTTTTTTT TTTATTGAGA 360
TGGAGTCTCA CTCTGTCACT CAGGCTGGAG TACAGTGGTG TGATCTTGGC TCACCGCAAC 420
CTCTGCCTCC TGGGTTCAAG CGATTCTCCT GCCTCAGCCT CCTGAGTAGC TGTTATTACA 480
GGTGTGCACC CCACACCCGG CTAATTTTTG TATTTTTAGT AGAGACCGGG TTTTGGTTTC 540
TCCATGTTGG CCAGGCTGGT CTTGAACTCC TGACCTCAGG TGATCTGCCC GCCTCAGCCT 600
CCCAAAGTGC TGGGAAGGAC ACACTTTTAT AAGCAGGCAT CTTTGGAGAT CTTGGTGGGA 660
GAGATGGCTC AAGGAGAGGA AAAGAGGGAG GTATTAGTAC AACTGGGTTT TTATAGGCCC 720
AGCACTAGCT TCATAAAAGT TATTTGCAAA AAAAGTACGG GTCTGTGTTT TTGTCTGATG 780
AGGTGGCCCA TTGCTCTATG GTAAGTGGAA TACATAATTG CTCACCTTTG CTTTTGGAAA 840
TTAAATGTAT TTAGAATTGA AACCAGCTTA TGGTTTTCTT CTCTTACTCA TGTTCATAGA 900
AGATGATCCT ATGAGTAACA CTTTTTTTGG AGACTCAATC ATTGTTTCCA GTCTCTTGCA 960
TTCTCTAGTA GGTGGTTTAT CTTCAGTAAC TTTTGCAAAT TGCATCAACA TACTTGCCTC 1020
CTACAAATTT AAACTCAATA AACCAAGGAG AACAAGGGTG TGATGGTGGG AATTTCTTTT 1080
GAAAGAGTCA AGCCCATGCT GTGCAGGCTG CACCCATCTT TACTGCATTC CCATAAAAGG 1140
CTTGGGGGAA GGAAGTTAAA CCATAACCCC GTTAGGTAAT AGGCTATGCA TTAATGCAAT 1200
TTATCTGGAA TGAGGAAGGA AGAGATTCAG CTTTGAAAGA ATTTCCTCAA CAGCATATTC 1260
CTCTTTGCTG CAAAGCTGTT TCACTTCAGG TGAGACCCAG GAAGCAGCCT GGGAATTCCT 1320
TGACCATCGA TACCAAAGGC TTTCTGGAGG TGTGCAGTCT CTAGGGATTT GAGGGTGTCG 1380
CCCAACAGTC AGTGTGATTT TACAACCAGT TCTCTCTAGG CTAATTTCTA ACGCAGGGAA 1440
TGAGAATGGT CATGCTGAAA AGTGGTAGAG AGATTTGACT CGCCTGATTG CAAGGACCAG 1500
GTCTACCACC CAGTAATTGT GTGGACTAGA AGGTGGTGGA GTGAGTAGTG ACCTCTGAAG 1560
AGTGTGACCT CTCAAGCCAA CTGCTTGAGC TCCAATTCTG CCTCTGCTAC TTTGTGACTG 1620
TGTAGCCCTG GGAAAGTTAT TTTACCTCTC TGTGCCTCAG TCATTTCCTC TATAAAATAG 1680
GTCTCTATAT GGACCTACCT TATAAGGTTG CTGTGAGTGG CACATGCAAA TGTGTTTATA 1740
AAGTATATCC CATGGTATGT GGCGTAATTT ATTTTTTGAG GGGAGATAGT GAGGTGCTAG 1800
TTACACACTG GGATGAGGTA GATCCTTGTT TGGATCTCAG CCTTGCTGCT CCCTGGGTAG 1860
GTGGCTTTGG ATCGCTGCTC ACCTTGCCAG GTCCCTCTGG CTCCTCCTTG GCTGAACATG 1920
CTTTGACTAC ACTGACCTTT CTGTTTCTCC AGCCCTCCTC ATGGCCTGTA TATAATATTT 1980
CTTCCAGTTG GAATGCTCTC TATTAACCAT TATGATTCTC ATGAAGGCTG TTTCTGTTCT 2040
CCAGGCTGGG TTCAGGTCTC TGTGATATCA CTCAAGGAGT TTTGTACCTA CCCTCCTGAG 2100
CACTTAGAAT TATGCTAGAG TATTCATTTG TATAATTACA GTTGACTCTT AGGCAGCTCC 2160
AGGGATGGGG 2170
|
