| Tag | Content |
|---|
EnhancerAtlas ID | HS175-25250 |
Organism | Homo sapiens |
Tissue/cell | SK-N-MC |
Coordinate | chr6:6699590-6702660 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Myod1 | MA0499.1 | chr6:6702322-6702335 | AGGGACAGCTGCT | - | 7.52 | | Sox3 | MA0514.1 | chr6:6699844-6699854 | CCTTTGTTTT | + | 6.02 | | Stat6 | MA0520.1 | chr6:6700870-6700885 | CTTTTCCAGAGAAAG | + | 6.02 |
|
| | Number of super-enhancer constituents: 26 | ID | Coordinate | Tissue/cell |
| SE_00137 | chr6:6694642-6702215 | Adipose_Nuclei | | SE_09354 | chr6:6699478-6700975 | CD14 | | SE_23153 | chr6:6698576-6701666 | Colon_Crypt_1 | | SE_23153 | chr6:6701732-6702739 | Colon_Crypt_1 | | SE_23777 | chr6:6699709-6701601 | Colon_Crypt_2 | | SE_23777 | chr6:6701845-6702653 | Colon_Crypt_2 | | SE_25016 | chr6:6698463-6702747 | Colon_Crypt_3 | | SE_25558 | chr6:6696674-6706299 | DND41 | | SE_26283 | chr6:6699285-6702431 | Duodenum_Smooth_Muscle | | SE_26869 | chr6:6699304-6701163 | Esophagus | | SE_27854 | chr6:6699368-6701551 | Fetal_Intestine | | SE_28835 | chr6:6699315-6701543 | Fetal_Intestine_Large | | SE_29666 | chr6:6698454-6702811 | Fetal_Muscle | | SE_32005 | chr6:6699315-6701521 | Gastric | | SE_33501 | chr6:6699318-6702786 | H2171 | | SE_34700 | chr6:6693551-6702714 | HeLa | | SE_37281 | chr6:6698710-6703829 | HSMMtube | | SE_39822 | chr6:6699426-6702759 | Jurkat | | SE_42348 | chr6:6698980-6701149 | Lung | | SE_48756 | chr6:6699674-6701616 | Right_Atrium | | SE_49964 | chr6:6698514-6702743 | RPMI-8402 | | SE_50192 | chr6:6693889-6702773 | Sigmoid_Colon | | SE_52541 | chr6:6698506-6701509 | Small_Intestine | | SE_52541 | chr6:6701653-6702763 | Small_Intestine | | SE_65078 | chr6:6699349-6701477 | NHEK | | SE_65078 | chr6:6701690-6702757 | NHEK |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr6 | 6699682 | 6701552 | | chr6 | 6701696 | 6702600 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH06I006699 | chr6 | 6698701 | 6705486 |
|
Enhancer Sequence | CTTGGCCTCC CCAAAGTGCT GGGATTACAG GTATGAGCCA CTACACTTGG CATTTATTTT 60
AAATAAAATT TTTTAAAAAG AGACAAAAAG AAACCTATCT ATTGTTAAAA CTTGTCCTCA 120
ACTCCAGCTG ATGACTACAA AGAAATGGAA ACAAAATGAA GACTCAATAA AAGTGCCCAT 180
AATCTTCTAG TCTCCAGTCT GTAGAGACAC AGAAGGTGAG AACTGGAGAG GCCTTAGAGG 240
TCAGCTCACC AATGCCTTTG TTTTGTGGTT GAGGAAATCG AGACATGAGG TCACTGGGAG 300
GTAATGGCCT TGCTAGGATT AGAACTCACA TCTTCAAACC TGAGCCCAGT GCTCTACCTG 360
AAGACTTTCC ACATACAGGG CATGACTGTC AATGGGGCAT GTTGGACTCC TTCCTGCACA 420
CCAGCGCGTG AGAATGAGGC ATACTGAAGA GTTAGTCAAG GGAGAGAACA TGCACCCTCT 480
TATGGGAACA CCATGGCCTT TCACATAAAT GTTTCACTGA GGGCTGGTTC ACAGGAGGTT 540
GGTGGTACAT GACCAGTACT GCAACAGTTA ATTTACTCTG TCTCATGGGA ACAAGTCAAT 600
AGGTTGATCG TAGTCGCTGA GTCTAACATG CTCCCAGCTT GAGCTGCACC CACTCTGTAA 660
ACAGCCCCTA ATGGTAGCAG CTTTACCCAC AACAATAAAA CGGCTCCATC TTCAGGCAAG 720
TCCAACCTTT ACCTCTCCTC CCTGCCCCTC GCCTGCCTGA TTTTAGACAC TGTTCTCATT 780
CCCAGGGACC GGGTTGCTCC CAACTTGTTG CCATAGCCAC AGGCCTCACC CAAAGCATAC 840
CAACGCTGTA ATGCTCACAG ATCTTGGCAG ACATCCAGGC AGATGCAGAG CAGTTGGGGT 900
GAATAACGTT CTCCTCTGAA AGCTGGGCCA AGGCTGTTTG GTTGCACTCT CTCCGCTGTC 960
GGCTTGAGTC TTATAGAGCT GTCCATTTGG CTGCCTGGCT GTGAATGAGC CATGGTTGTT 1020
AATTTCTTTC CCCTGCATCA GCTTCTTGGG AGCCTCTAAC ACAAAACTTA AACAAAGAGC 1080
TAAATCAGGC TGTTCCCAGA GCTCCGGACC CTGGCTGTTT ACCAAACACT GAAAACGTTA 1140
CCAGTTGCCA CCAGTCCCAA ATCTCTAATC TCTTCTATCT AAAAGTCGTG AGGAATGTTG 1200
TCCCGAGAGG TCCAGGCCTG GCCCATCTGT GATGCTCTTG GGTGTCCGTT TCAACATCGC 1260
AGTCCTGTGA GTTGAAGTAT CTTTTCCAGA GAAAGAAATG AAAGACGGGG GTGGGGAGTG 1320
GGGTGAAGGA GCACATGGCA AAATAGAGAT GGAATCCCTT CAAAAACAAA GAGGAGCCGT 1380
CCATGTGCAG CGTGTTCACC CTTGGATGAT TTATATTGGC CCAGTGCTCC AGTTCATGGC 1440
AATTACAAAG AAGGAGGGAG TGTCAGAAGG AATCTTCCAT GAATACCAAC AGTACCAGCC 1500
AACATCTGTC CCTTGGGGTG GGCAATCTGC TCCAGCCTGT TCAGAATTCT ACTTAGAATT 1560
CTCAAATGGG ACAGTGAACA CAGAGGCACT CTGTAGGTTA GAAAACAGTG CATACTGGTA 1620
GAATGTTGTT TTCATCAGGC ATTCCCTTCG CTCCTCCATT GGCGCTCATG AAGTGAGTTA 1680
AGTCCCTCGG CCCCTGCCCC AGGGTATGTG CCCACATTGC CATAGAACCT GCCTGGTAGG 1740
GAGAGGGCTC ACAGACCTTC TCCCACATGA GAAGGGATTA GGATGGGGGT GGGCAGGGGC 1800
CACTTCTGCT GATGAGAACA CAGCAGTTCC AATCTCCCTG GAACTGGCCC CCAAGCCCCC 1860
TCTCCCCAGT TGCATTTCTG CATTGATTTC CTGCCCAGAG ATACTTCACC CGCAGTTGCC 1920
ACGTCTTTGG CTAAGGAGTT GCTTTAAAAG AGAATACAAG ATTTAGATTT AGCTGCCTGG 1980
AAGAGGAAGG TGTTTTATTC TTCTTTAAAG GTAGTCTGGA AAATTACCAC TTTAGTGGGG 2040
GGAAAATATA CTCTTCAATT AATAACATAA AAACGAAGCT GGGTGCAGTG GCTCACACCT 2100
GTAGTTCCAG CACTTTGGGA GGCTGAGGTG GGAAGACTGC TTGAGCCCAG GACAAGACCA 2160
GCCTGGGCAT CATAAGGAGA CCTCATCTCT ACAAAAAAAA CCTTGAATTT TTAAAATAAA 2220
ACCATCACTA CGACTAACTT TTAACAACAC ACTCTAAGAG CAGGGGAAAA AAAATCCTGG 2280
GTACTAATGC TGAAAATGCA TATATTCCAA GGAATGGTAG CCATCATATC CCCCGTATGA 2340
GACAGAACGA TTGAACCAGA TCCTACACAG CTTGCCTCAA ATCCCTGGGC AAGACTTGCC 2400
ACAAATCCTG AACTTCCCTT CATGTTGTCT TTCCATAATT CCTTCTCCTC CCAGCACCAA 2460
CATCAGTCTG ATTTCTAATA TTTAAACCAC CAGAAGCTGG GCAGAGCCCA CCCAGGAAGA 2520
ATTCTAAAAT GTCATTAACA AATACAGCCT GAAATGGCTT CAGAAGTTGC TGACACTCTG 2580
TTGAGACAGT GTCTTTTGAA AGACAAGGAC AGTTGAAAAC TTCTTGCACC ACTGAAGGCG 2640
GCGCCCTCCT GCACGTTAAC AGTTTCTCCC TCCACCACAC AGTTCGCTAT CTCTCCATCG 2700
CTGGCATTCA TACGGCCTCA CCCATCTCCC CGAGGGACAG CTGCTCCCAG AACCACCCTG 2760
CAGCTGAGCA GCAAGATGAG CAGAATTTTC CCTGTGAGCA GGAGACAAGG CTAAAGCTGC 2820
ATGTGTGTCA ATCGTGAAAG CCCAAATCAG GAGACAGATT AGGACTCTAA GGGAGCTCCA 2880
CTTACCGAAG ACCATCTCCC CAGGAGAACA GGCACTGAGG GCCGCCCACC CCCACCACGC 2940
TCTTTTCTGA ACAGATAAAG GGAAACTCAC ATTTTTTTTT TAAACTGAGT TTTGAGTCTT 3000
TGGGAAGCTC GTATGCAGTT GACACCCGCT GACTTCTGGA GACATTTAAA AAAAAATTAA 3060
AAGCATATTA 3070
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