| Tag | Content |
|---|
EnhancerAtlas ID | HS127-02702 |
Organism | Homo sapiens |
Tissue/cell | Macrophage |
Coordinate | chr1:206844730-206848360 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CDX2 | MA0465.1 | chr1:206847320-206847331 | TTTTATGGCTT | - | 6.62 | | IRF1 | MA0050.2 | chr1:206847243-206847264 | GCAAAGAAAGAGAAAGAAAGA | - | 6.1 | | IRF1 | MA0050.2 | chr1:206846377-206846398 | AAACAGGAAGTGAAACTGACT | - | 6.75 | | MEF2A | MA0052.3 | chr1:206846059-206846071 | TTTATTTTTAGA | - | 6.07 | | PHOX2A | MA0713.1 | chr1:206845362-206845373 | TAATTCAATTA | + | 6.14 | | Phox2b | MA0681.1 | chr1:206845362-206845373 | TAATTCAATTA | + | 6.14 | | RELA | MA0107.1 | chr1:206845879-206845889 | GGAAATTCCC | - | 6.02 |
|
| | Number of super-enhancer constituents: 20 | ID | Coordinate | Tissue/cell |
| SE_00569 | chr1:206845430-206847366 | Adipose_Nuclei | | SE_26063 | chr1:206845203-206849485 | Duodenum_Smooth_Muscle | | SE_27575 | chr1:206846160-206847114 | Esophagus | | SE_27575 | chr1:206847359-206849345 | Esophagus | | SE_28475 | chr1:206844512-206849593 | Fetal_Intestine | | SE_29888 | chr1:206844751-206846991 | Fetal_Muscle | | SE_29888 | chr1:206847969-206848969 | Fetal_Muscle | | SE_31968 | chr1:206847920-206849125 | Gastric | | SE_40319 | chr1:206844654-206848703 | K562 | | SE_40628 | chr1:206844652-206849539 | Left_Ventricle | | SE_42239 | chr1:206844942-206849550 | Lung | | SE_45992 | chr1:206845606-206849606 | Osteoblasts | | SE_48619 | chr1:206844750-206847180 | Right_Atrium | | SE_48619 | chr1:206847942-206848995 | Right_Atrium | | SE_50514 | chr1:206845185-206847147 | Sigmoid_Colon | | SE_50514 | chr1:206847793-206849468 | Sigmoid_Colon | | SE_51178 | chr1:206847613-206848993 | Skeletal_Muscle | | SE_52589 | chr1:206844796-206847319 | Small_Intestine | | SE_52589 | chr1:206847770-206849390 | Small_Intestine | | SE_54245 | chr1:206845387-206847187 | Spleen |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr1 | 206845391 | 206846936 | | chr1 | 206845419 | 206847733 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I206671 | chr1 | 206844732 | 206849398 |
|
Enhancer Sequence | CCAAAGTGCT GGGATTACAA GCATGAGCCA CCGCGCCCAG CCTGGAATTC TTAATAATTT 60
CTGAACAAGG TGCTATGCAT GTTTATTTTG CACTGGGTCC GGCAAAGGAG CTAACTGGCC 120
CTGAACAGAG GTAGGGAACT AAAGAAACTC GTCTTTTACA GGCTCGGAGA TGCCAAGACA 180
GCCAGGGTGG AAATGCATAT GAATGATAAT GTCCTAATAG TAGTAGTCTA TTTCACAGGG 240
TTGCTGCAAG TGTTGAATGA GAAAATATGT GGAAAGTGCT TAGAACAGTG TCTGGCACAT 300
AGGGAATGCT GTGGAAGTGT TTGATATCAT TACTGTTCCC TCCTTGTACT GGTTCAACAC 360
CTGACAGCCT GAGGTTGATT ATTCAAAGGG TCACAGTGGG CTTTTCTCAT TTTCCCATTT 420
CTAACCTGTC GCTCACCATC CAGCCCCAGG CTTATGATTG TCCTTTGGGG GAAAAAACTC 480
CAACAACAAT AATTATCACA ATAAATACAT AGGTGAGATC ACATCCTCTC TTGATCCTTA 540
GTGTAGCTAG CTGGTGCTTC AGGGTGTGTC TGTGTGCTCT GTGTGTCTTT GTTTGTGTCT 600
GAGAGGGAGG TTTTTTTTTT TTCATTTAAT TTTAATTCAA TTAATTAGAG GCTCTCTCTG 660
GTGGTTTCAT TTTGTTTTTC TTTACCTGCC TTTTTGGTTC ATATAGCGAG GACCCTGGAA 720
CCACCTGCTT CCTCCCTGCC ACCGCTTCTC CTCAGGTCCC CAGGGGAAGC CAGGATCTAA 780
AGGATGACTG TGTCACCATT GTCCTCAAGA TAATGGCTCC CTCCCCCGCT TCCCTCCACT 840
CCTATCTCAT TCTCTTGAGC CTGTGGAGTG TTCAACCTTT GTCCTTCGAG TATAACCCTT 900
TACTGGCGAT AAAAAATTAA AATACTGGCT CAACACCTCT ACTCCACGAA GCTGTTGTCT 960
TGACCAAAGT CTGAAAGCTG CCCCTCCTAC CCCTATTCTA ATCTTAGACA TTCCCAGCAC 1020
ATTCTTAGTA AGAGGGAACT CTCTCTCATT GTCCTAGGAT TTTAAGTCTG CAAGAACTAC 1080
GCATTTTTTT TTCCTTAGCA GAAGCAGTTG TACTTTTTCC TGACAACTTT GCAAGTTCCC 1140
CATAAAGTTG GAAATTCCCT TCCTCGTTAC AGCTCTTGAT AGATGCAGAA GAAGCCTAGT 1200
CTGGACCTGT CTTCTCTCCT GACCTGCTGT GTAACTCTTG GGAAGTTAGT TTAAATGTTT 1260
TTGGGCCTCA GATCACAGAG ATTAACTTGA CTGGGGACAG ACTGAAGGCT GAAAAGTGTT 1320
TGGGAATGAT TTATTTTTAG AGGACCTTGG GAGAAGGGTT TTACAAATGT CTCTAAGGTA 1380
AGAATAGCCA TTTGGGGAGT TACCAAGACA CTTAGATTCC CCCTCCTGAA AAAATGAGTT 1440
TAATAATTTC CATTGCTAAT TTCTATGTCC CCACCCTTTC CTCCAAGCCT GCCTCCACCC 1500
TCAGCTGTTG ATTGATGGAG TAGATGTGCT CTACTCCCCC TCCCACTGAT GCACACACTT 1560
CTGGGAGGCC CTATATAAAT AGAAGCCAGA GGCAAGGCTG CAGAATTATT ATTATCATTA 1620
TGATGATGAT TATGTTTTCA GCATGAGAAA CAGGAAGTGA AACTGACTAA AATGCCCAGT 1680
GATATGTGGC TGACCCTGTC TCCTCAGCTG GACCTAAAGG CAAAGGAGAA ACTGGCCAAA 1740
GAAAACTGTA GCCCTGCCAC AAGCTTTAAC AACTTCTGGT GGTGTGTGTG TGTGTGTGTG 1800
TGTGTGTGCG TGCGTGTGTG TGTGTTACAA GGAGTGTCTT TAAATAAGCA GCTTCTAGAA 1860
CTTGTGATCT TTCAACCTTA TTTTTATGCC CAAGCTTCCC TCTTCATGTG ATATCCTCAG 1920
AGTTCTTCCT TACTACTTCC TTCCCCATTT CCTAGAGAGA GCTTCTCACG GCTGTCAGAA 1980
GATGTTAAAG GAGAAGTCCA ATGATTAATT ACTTCCCACT ACACATGCCT TATCTGCCCA 2040
GGCCAGGTCT GAGCTGTGTG CCTTTCTTGA TCACCGGGTC TGTCTCCAGG GCAGACATAT 2100
TCCCTGGGCC CCCAAGGCCT TTCTTCCCTC TCCCTTCAGG GGGCCATGTT TTCTCTTCTG 2160
CCTCACTGCT TGAGGCTCCA TCTGCTTGGT TGATTATTCA TGTCCTTTGT CTTTTTCAGG 2220
AATCGATTAT GGATAAATGG TAGTTAGAAA ACAGGGCTTC AGGGCCGATG TAATTATCCC 2280
ACTTTGACAT TTCCATTTTC AGCACCATGG CCTCTGGAAA CACTGACACA GTGAAAATGA 2340
CCTGATTTTC ATACTACCTT GTTAGTTCAA CTTCCTAGGG AGAAAAAAGC AGGCAGCTAT 2400
GTGGAGAGTA AATGAACCAA GTTGGTGTTT CAGAAACGCC TCCTCATTTG GACAATATTC 2460
TGAAAAAAAA AATGCATAGG AAACAGAAGA GAAAAAGGCA TCTGCGGGGG ATAGCAAAGA 2520
AAGAGAAAGA AAGAGCATTT CAGCTGTGCA GGGCATTGGG CTCACATTCT GGTCCCTGGG 2580
CCCACACCTT TTTTATGGCT TTCATACCAA GATCTCGAGC TAGATTAATA GATTATTGGA 2640
ATTTTGGGTT GGGAAAAACA TAACTGTCTT ATTCTCGCTA TAATTTTTTC TGAGCCTAGA 2700
ATAGGGGGTC CAGCGAAGTC CACCCAGGAG CTGGGATGGA GGATGAGGAT CATAACAAGG 2760
TACTTGATTG AGGAAGAACA ACTCTAGTAT GGAGCTTTAT GCCCCAAATT GCAGCAGTTA 2820
TGAGTCTTAC TCCCTGCATA GGAGAACATG GTGGCTGAGA AGACAGGTGT TAGTTAGGTC 2880
CCGGCTTTCT GCATTCAAAT CCCCACTCCA GACCTTACTT TAAGTTGCTT AAATTCAATG 2940
GGCCTCAGTT TCCTCATCTG GGCCCCTGGA AGGATGTTAG TAACACCTAT CTTGCAGGGT 3000
TGTTATGGGG CATTGATTGA GTCAACACCT GGAATCACAG GCATTGTAGG AACATAATAG 3060
GTGCTCACTA AAAGAGAGCT ATTACCGTGA ACTTTTAAAT TTGTCTTTGT CTATGTGCCA 3120
TTCACTATCC TCCATTTCAT CCATCCAGCA AAAATACAAA TGCCATATTC TGTGACAGGC 3180
GCTGGGCAAG TCACCAGGGA TAGACACAAA GCAGAATATA AATCTTGTCA GAGGATTTAT 3240
CCTCCCCAGG TTTCTCTTAT TTCTTAATCC AGAGCAGAAC ACATAACAAG TTTGAACCCA 3300
ATTTTCACTG TTCCTTGGTC CTGTTCCTCA CCCATTCTCT CCATTTGCTT TTTCTGCTTC 3360
CTTGCTCTTT CTTTCCCAAC TCTGTAGGAA GATAGGCCCC AGGTATCTCT GCCAAGGAAG 3420
GTCCCTGGAA TCCTGCCAGG CTCTTCTAGG ACTTGTCTTG GTGAGGGAGC CCTGGGAGGG 3480
GCAGGTCCCC AGGGAAGCCT GTTGCTCCTC TCACTCAGCA ATCCCTCTTG GGCCAGGCTC 3540
CCCTTCCCAG GCCCTCAGCT CTCCCACAAG ATCTCTGGGG AAGCTGGAAG AGGGCCACTA 3600
GGCCCTGTAA TAACCACACT TCTTCATGGT 3630
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