| Tag | Content |
|---|
EnhancerAtlas ID | HS170-00754 |
Organism | Homo sapiens |
Tissue/cell | RS4-11 |
Coordinate | chr12:11901720-11904640 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ALX3 | MA0634.1 | chr12:11902169-11902179 | TTTAATTAGA | - | 6.02 | | PHOX2A | MA0713.1 | chr12:11902166-11902177 | TAATTTAATTA | + | 6.62 | | PROP1 | MA0715.1 | chr12:11902166-11902177 | TAATTTAATTA | - | 6.32 | | PROP1 | MA0715.1 | chr12:11902166-11902177 | TAATTTAATTA | + | 6.62 | | Phox2b | MA0681.1 | chr12:11902166-11902177 | TAATTTAATTA | + | 6.62 | | RREB1 | MA0073.1 | chr12:11902215-11902235 | CCCCCATACACACACACACA | + | 6.01 | | RUNX1 | MA0002.2 | chr12:11904362-11904373 | AAACCACAGAC | - | 6.62 | | Stat6 | MA0520.1 | chr12:11903257-11903272 | GAGTTCCTAAGAAAT | + | 6.08 |
|
| | Number of super-enhancer constituents: 20 | ID | Coordinate | Tissue/cell |
| SE_09138 | chr12:11895682-11929433 | CD14 | | SE_12874 | chr12:11901895-11903319 | CD34_Primary_RO01480 | | SE_13315 | chr12:11894774-11907169 | CD34_Primary_RO01536 | | SE_14048 | chr12:11894835-11905878 | CD34_Primary_RO01549 | | SE_25772 | chr12:11901458-11913877 | Duodenum_Smooth_Muscle | | SE_30380 | chr12:11902402-11903491 | Fetal_Muscle | | SE_30906 | chr12:11895997-11913332 | Fetal_Thymus | | SE_32458 | chr12:11895992-11906916 | GM12878 | | SE_39367 | chr12:11903203-11903675 | Jurkat | | SE_43859 | chr12:11901535-11908049 | MM1S | | SE_49833 | chr12:11903268-11909634 | RPMI-8402 | | SE_51622 | chr12:11902392-11904302 | Skeletal_Muscle | | SE_54656 | chr12:11902989-11904309 | Stomach_Smooth_Muscle | | SE_58379 | chr12:11878906-11990784 | Ly1 | | SE_58837 | chr12:11874923-11935776 | Ly3 | | SE_59849 | chr12:11874575-11943335 | Ly4 | | SE_61023 | chr12:11869475-11929777 | HBL1 | | SE_61926 | chr12:11879670-11927640 | Toledo | | SE_62748 | chr12:11877030-11934459 | Tonsil | | SE_66238 | chr12:11903203-11903675 | Jurkat |
|
| | 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 |
| GH12I011743 | chr12 | 11895936 | 11914068 |
|
Enhancer Sequence | ATTGGCCCTT CATGGCTAGG GGAGAAATGG GAGAGGGAAC GCAGCTCATT TTGGCTTCAG 60
TCCTTACGCT TTCAAGAGAC AACCCTACTC CATACTTCAT TATTTTTTTT AAAGCTTTCT 120
ATAATGGTTG GTGAAATTTA CATTTCAACT CTTGCCTACA ACAGTTTTCT GCCTTATTTT 180
CTCTTCCCAG CGCTTTGTGC CGCCTCCTTG ACAACCTGCT CATAGGTATT ACAATTGGCC 240
TCAGAAATTG CAGTGCTTCC CTTTTGTTCA GCTGGTTGGC TTGATAGGTT GTATCTGCAA 300
ATTTGAGAGC AGCGTGTTTT ATTTTTTACA GCATCTAAAC AATAATGTAA CCACATCACG 360
GCATTCTGAG TCACATCATT GACCTCCACC AGCAGTTTAT CCCCCTACAA CACTTGAATA 420
CATTAATATC ACTGTCTGTA GCATTTTAAT TTAATTAGAG CAGCGGTTAT AATCCTCTTG 480
GGAAAATCGT TATCCCCCCC ATACACACAC ACACACACAC ACACACACAC ACACACACAC 540
ACACACACAC ACACACACAC ACACCCCTAC TCCCCATAAT GTTAAAAGAA AGAAAGCAGC 600
TCTGGTTTTC ATCTGTCTGA CAATTTGCTT TAGAGGTGGG ACTCTCACCA CCACCCCCTC 660
CTTTGTTGGG GTCGCACCAG AGAAGCAGTT GTGAGAGTAA AGAGGTTCCC TTTATTTGGG 720
AAATTAGACG TTAGTGTCCT TAAACTTCTC TGTCTAGATG TCTCCATCTG AGATAGTGGT 780
ATTTGGTTAA TTTTTCCAAT TGCTGATAGT CTGCTGATGT GCCAGGGTAG ATGTTAAGTG 840
CGAGGTTATT GCAATAGAGT GAAAAATGAG CACTGTGAGA GTCAACCTAG AGATTCACAA 900
AAAGAGAGAC AAAAGGAGTC TCTGTAGTGT GGGATTCCCA AGAGTGTGTT TTGTTCTCCT 960
TGGAACAGAG CCCACTCACT GTACAGCATC CTTTTGGGGT CCCCAAGTGC TCTGCAGCCA 1020
CCAAGCCCAG AGTTACCTTA GGTGTGCCAT GGCTACTAGA AGAGTGCTCG GGGCCCTAGA 1080
AGCACATTGT GCATTTGTCC GTCTTGGTCA AGGTAACCTC TCTTGTTGCT GACAAGTCTC 1140
TTCATTGAGC CTTTGAAAAA GAGCTTATGG TGTGGAAAAC TGTCCTCCAG CTGAGTAGAA 1200
ACCATCATCA GGAATGTGAG GAGATCAGTG GGCCACAGTC TCTTCATCTC TGGCCTTCCT 1260
TTTATAAGTT TTCATCATGA AATAGCAGTT GTCTCCATCT AAAATTGTTT GGACGGGGTT 1320
TGCGGGGGAT GGCGTCAGAT CCCAGAGCAG GTGCAGAAGT GTGGTGTTTC ACCGTAAGGT 1380
CAGGGAACCA TGTAGAAGTG AAAGCACACC AAGGGGTTAC TTTTAAAGAG AGCACAGTTG 1440
AAAGGAAGGT CCAAAGCAAT GATAATTTAG TAAATTACAG TATATACACT TTCAGGGTAA 1500
TAGCTAGCCA GACTCTTTTG TCAGCTGGCT GGGGATGGAG TTCCTAAGAA ATGAAGTCCA 1560
GTCAGCATGG AGGGCCGGGT TTCTCCCAGC TTGCCTTGGT GGAGTTGGGG CAGGCGGGGA 1620
TGAGGCGGCC TCACTCTCAT GGACTAGCCA GAGTGTCTTG TGAGTTTCTC TTTGCTTCAA 1680
GGGAAAGAAG AGTCATTGAA TTTCGAAATG CTGTCTTGTT TTTTTCTTGC ACTCATGAAG 1740
CACCATTTGA AGACCCTTTG GCTGCCCGAT GTTTTCTTCA CCAAGTTTCA CTTCTGCAAA 1800
AACCCTAACA AAACAGAAAG CTATTTCCGA GAATAAAGTT AACGGTAGAT ATCTAGACAT 1860
ATAGTGGGAT TTGGGGGGTG TCAGACAAGA GTTGAAGAGT ATGGAGAATT TGTTAAATTC 1920
TAAAAACAGA CTGTTTGAAA TGCTCAGAAG CCCACCTCAC CTTTAAAAAC CTCTGAACAG 1980
ATTTTATGTT TCCTATATGT GTGGGCTTTT TTTTTTTTTT TTTTTTTTTT TGCTTTTTTC 2040
ATCCCAAACC AAACACCAAA AAGTATAACC CATCCTTCAA GTTAAAGTTT CTCAAAATAC 2100
ATGTGATGCC TGCTAAAGTT CAAGAAAAGT GCAGTTGAAA GTTTTGCCTC TGGGTGACTT 2160
TTTACAGGAC ATCTTAATTG ACCCAGAAAT GAAACCTGGG ATATATGTGC CTGCCCTTCA 2220
TTAAGAAATT CACCAAGAAA CCTCAGGATG TATGTTTAAA CAGAAATATT CCAACTGCCC 2280
TACTTGCTTC TGGTGGGTGC CTTAGGGAAG GTATAGCAAT TCCATTCGGA AATTATAACA 2340
ATATGTATAT ATTCATTTAA AATCAAAACT TCCTACCACA ACTGCCAGAC TTTCTAGGCT 2400
ATGAGCAGAG GAGAAGCTTT AATTTGGTTA TAGGCCGAGG ACTCCGCCGC TTCCCTTTGC 2460
ACATTTGATG AGATGTAAAA TGTTAAAGAA CTATCTTTCC AAAACGTAAA CACTGCCTTC 2520
CCTTTACTTA AATGTACGAT TTTCTTTTGC TCTTGAGTTT TATTTTCATA GTGGCATCTT 2580
ACTGGTCTTT CCTTTCCACC ATATTTTTGG ATGTTGTGTG TTCCATTTTA CATTGCCCAG 2640
TTAAACCACA GACACTCCTG AAGTCATGTT TACATGTGGA CTGCAAGTCA ACCTAGTTGG 2700
CATGTTGATC TAAGCTACAA ATTGCACTGC TGTTTTGCCG AACCCAACAG TCGGTTTCTT 2760
GCCATTATTT GCGGTATTTT AACTTAAAAC TCACGGTAAT CCTTCTCACC CCATCTAGTT 2820
TGTTTTAATT GATCTAACAA ACACTGCTTG TTTGAATTCA AATGGAGGAT CCATGGAAGC 2880
TCTCCCACCC CACCCTTTGA TACTTGATAA GGGGTCAAAC 2920
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