| Tag | Content |
|---|
EnhancerAtlas ID | HS044-06436 |
Organism | Homo sapiens |
Tissue/cell | Fetal_kidney |
Coordinate | chr19:6065630-6068280 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| KLF16 | MA0741.1 | chr19:6066005-6066016 | GGGGGCGGGGC | - | 6.02 | | KLF5 | MA0599.1 | chr19:6066006-6066016 | GGGGCGGGGC | - | 6.02 | | SP2 | MA0516.2 | chr19:6066003-6066020 | CTGGGGGCGGGGCTGGG | - | 6.03 | | ZNF263 | MA0528.1 | chr19:6066122-6066143 | GGAGGAGGTGGGGGAGTGAGG | + | 6.81 |
|
| | Number of super-enhancer constituents: 25 | ID | Coordinate | Tissue/cell |
| SE_00353 | chr19:6065551-6068885 | Adipose_Nuclei | | SE_01604 | chr19:6065279-6066959 | Aorta | | SE_01604 | chr19:6067055-6071713 | Aorta | | SE_09597 | chr19:6059621-6068905 | CD14 | | SE_12907 | chr19:6064951-6068518 | CD34_Primary_RO01480 | | SE_13400 | chr19:6064969-6068546 | CD34_Primary_RO01536 | | SE_14082 | chr19:6064531-6068692 | CD34_Primary_RO01549 | | SE_23458 | chr19:6065493-6068455 | Colon_Crypt_1 | | SE_24248 | chr19:6065543-6067898 | Colon_Crypt_2 | | SE_25797 | chr19:6054521-6073197 | Duodenum_Smooth_Muscle | | SE_26679 | chr19:6065483-6069956 | Esophagus | | SE_29788 | chr19:6065358-6069204 | Fetal_Muscle | | SE_35921 | chr19:6065744-6068092 | HMEC | | SE_37314 | chr19:6064942-6068309 | HSMMtube | | SE_38048 | chr19:6055954-6068597 | HUVEC | | SE_42288 | chr19:6065246-6069812 | Lung | | SE_44165 | chr19:6064089-6069731 | NHDF-Ad | | SE_44879 | chr19:6065469-6065995 | NHLF | | SE_44879 | chr19:6066023-6067990 | NHLF | | SE_49210 | chr19:6065256-6068547 | Right_Atrium | | SE_52794 | chr19:6065478-6069502 | Small_Intestine | | SE_54507 | chr19:6054642-6073245 | Stomach_Smooth_Muscle | | SE_64265 | chr19:6064909-6067966 | NHEK | | SE_65533 | chr19:6059953-6066138 | Pancreatic_islets | | SE_65533 | chr19:6066252-6068284 | Pancreatic_islets |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr19 | 6066698 | 6067208 | | chr19 | 6067299 | 6067617 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH19I006055 | chr19 | 6055612 | 6069370 |
|
Enhancer Sequence | AAACACAAAT GACATTCCAT TATAAGTTTC TGCTGCAAAA GAAAGTTGGG AAATTTGTTT 60
AGATACTTTA AATAGTCCTA AGATTAGCTG AAATGCCGGT AACAAACGTG CAATGAACAT 120
TTTCTTGGGG GCATTCAGCA ACAAAGTGAA TCGTCCTTAA AAAAAATCCA TACAACTAAA 180
GCGAGTCTCA CCACGGGAAC CACAGGAGCT GTTTTAGTGA GGGGCTGGAG TGTCTGTTAC 240
AGGCGGCACT TTTGCGGCTG TTGCTGCATT AGTCAGATTG CACTCGAGAT GAATGAGGAA 300
GAATAAAGTC TTCACCAAAA ACCTGTCTTG GCTAACAGTT CTGAATTTAT AGCCCTGGCA 360
GTGGGGGCGG GGGCTGGGGG CGGGGCTGGG AGGAGGGGAA GAAATGTGTC ACCCGCTCTG 420
AATGAAGTTC AGGGGTGGTG TTTACCTAAG CAACAAACCC TTGTCAACAA TCGCTATCTC 480
TGGCTTGCCA GCGGAGGAGG TGGGGGAGTG AGGCTGTTTT GATCAAAATC CAACCTGTGG 540
CTGCAAAGTG CCCATCAACA GGGCACTTTG TTAGTGGGAA CGTGCGACCT CTCTTAATAA 600
ACATAACATA CACATCCCAC TGAGGGCCAC GGGTGGACCC AACTTCTTAA CAGGAACATT 660
GAGCACATGA AACCAGAAGG TGCTGGGTCC AATTTCCACC CTCAGCCAAC CCTATCTGTG 720
AATGTCTCTA CATGTGAGCC AGCCAGGGCT CAACTCTTTG CTCTTCTGAA ATTCTTAGGC 780
AGCAGAAATG AAGGCATCGT GCTGAAAAGC GCTCCAGAAA TTGCGGATTT ATCAGTGATG 840
TACGGTAGTA GGTTGGACAA GTAATGATTT TCTGAACACC AGGAATTAGA TCAAAAAAGA 900
AATTCCACTT AAGACTAAAA TAAGTCTCCA GTTGAGAGCA GTCTAGGACA TATTCGAATG 960
GCCAGAAGTT TGTTTCAATG GGGCCTCTGC GTTTGTGCAG CCTGGGAGTC AACATTACAA 1020
TATTGGTTCT TTCAAGCAGA TCCCGAGTGG ATCCATGTCT GCCTGTTGTG GCAAATCAAA 1080
CTCAAATTTA ATCAGAGAAA AATATATGCA GATGTTCAAT TAAAACCTGG AGTCCGCAGT 1140
CTTGGCACTG TTTGCCCGGC CCTCATTGTT TGCTAAGTAA CAACGGTTGC CAGGGGCAAC 1200
GCAGTCCACT CCCGTTTCCA AGAGCCTGTT GCTGGGCAAC CGGGAGAATA CTTCCCAAAC 1260
CAAACAATGT CATCCCGGAG CAACCCCCTC TATCTCACAT TAACCAGATC TAAAAAAAAC 1320
CCTCTCAAAT ATGTAATCTA TTATTTTCAG AAGCCCTAAG AGAAAGGCAA ATAATCTCTT 1380
CTCTATAGTA ACTGAGGGGA AAACAGTTTA CCATATTTGT TCTGAAATAA CAAAACCCAA 1440
GGAGGAACAA CTCTCTCTGA GGTAAGAGGG CATCACAGGA GGGATTTCAA TCCTTCCTAG 1500
TACTGGGAGG AGAAAGTGCC CTTTTCTCCA AGAGGAAAGA ATCTATTTAT CATCAAACAA 1560
ACAATGTGGG AGAGTTCATA GCTGCACAAG TGTTTTCTGG GCGAAGTAAA ATGAATCATG 1620
GATTAAGCTA TTTGGAAAAA AGTGTGAAAA CAGAGGAGTT GATACCAAAT TAAAACGACT 1680
TTTGGAAATA TCATGTACGT ATGGAACAAG TGCAAAGGGA ACCACTGACT CAGCGTCAGA 1740
AATGCCTTGT GGGGCTTTGC CGGGAGGGAC TTACAGTATA TCTTTGACAT CACTGCGCCG 1800
GCTCTTCCCT CCCTACCCGG AGAGAGGAAG ACTTTTCTAA GAGGAAGCCA GGCCACATCA 1860
GATGCCCCCA GATGGCAGGA CACACAAGGG ACACATATCT CCGGAAAGAG GAGGCACATG 1920
GTTGGGCAAT CTCGACCCAT GAAGGGGGAA AAGAAAAGGG CTAAACTGAA GCTAGTGCAG 1980
CTTTTGTTCT GCCTGGAGCA GTTCAGGCTG AGCATGGCTT CTCTGAGGCT TTGGGACCAG 2040
GAGAGGGTGA AGTGGCACCA CCACCTTTCA AGGGGAACAC AGAGCTCTAA GCAGTGCTCT 2100
TGTTTTTGGT GGGCCCAGCC AAGGATCTTA AAACATTTTG ATAGAATGAG CAACATGTAG 2160
CTGCAGCCTC GATGGGTCAA CATTTTGGAT GATAAAAGCA CACAATGCTG ATAGATTTGT 2220
GCATGACCAA GCATACCTTT CAAGGAGCTC TCAGCGGAGG TTTGCCCTTT GAGACAGACA 2280
CAGTCAGTGC ACAGAAACTG TTTTTTTAAG ATATCATCCA GGAGTCATTC CTAGAATAGG 2340
AATGGAATAG ACATGCCTCC CTGAGAAGAA AGGAAGACAG ATTCTATACT GTTAGAATTT 2400
GAATCTGTGT TGCAGGGAGA TGAGGAATTT GAAGCCAGAC TCTTGGGCTG TTAATGTATG 2460
GCTAAGTGGT GATGTGGTGA CAACCTTGAA TGCTAGTCCT GGAGGTCAAA TCACCAGCAG 2520
CTGGTGCCAT GGGAGGCTTT GCTTAGGGGA CACGGCTGGG TTCTGCCTGG ATGCTGCATC 2580
CCAAGGGAGG CATTGAGGTG CGGCTGTGAG GACTCCAAAC CCCATGTCCA GAAGGATGAG 2640
TAACAGAGAT 2650
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