| Tag | Content |
|---|
EnhancerAtlas ID | HS098-19816 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr15:67466830-67469690 |
SNPs | | Number: 5 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HES2 | MA0616.2 | chr15:67469246-67469256 | GGCACGTGCC | + | 6.02 | | HES2 | MA0616.2 | chr15:67469246-67469256 | GGCACGTGCC | - | 6.02 | | RELA | MA0107.1 | chr15:67467407-67467417 | GGGAATTTCC | + | 6.02 | | TBX21 | MA0690.1 | chr15:67467969-67467979 | AAGGTGTGAA | + | 6.02 | | TBX2 | MA0688.1 | chr15:67467969-67467980 | AAGGTGTGAAT | + | 6.02 | | ZNF263 | MA0528.1 | chr15:67467455-67467476 | GAAGGAGGAGGCAGGTGGAGA | + | 6.44 | | ZNF263 | MA0528.1 | chr15:67467458-67467479 | GGAGGAGGCAGGTGGAGAGAG | + | 6.66 |
|
| | Number of super-enhancer constituents: 20 | ID | Coordinate | Tissue/cell |
| SE_09181 | chr15:67466836-67470715 | CD14 | | SE_10875 | chr15:67463174-67471168 | CD20 | | SE_18371 | chr15:67463340-67469893 | CD4p_CD25-_Il17-_PMAstim_Th | | SE_23212 | chr15:67466304-67468217 | Colon_Crypt_1 | | SE_26536 | chr15:67466309-67469672 | Esophagus | | SE_31411 | chr15:67466416-67469347 | Gastric | | SE_37787 | chr15:67466568-67472740 | HSMMtube | | SE_37941 | chr15:67465373-67472958 | HUVEC | | SE_38928 | chr15:67462159-67469899 | IMR90 | | SE_42172 | chr15:67467092-67469654 | Lung | | SE_44471 | chr15:67467419-67472425 | NHDF-Ad | | SE_44749 | chr15:67466055-67469674 | NHLF | | SE_45534 | chr15:67453126-67473814 | Osteoblasts | | SE_47100 | chr15:67357928-67475420 | Panc1 | | SE_48052 | chr15:67464183-67473310 | Psoas_Muscle | | SE_50064 | chr15:67466721-67469446 | Sigmoid_Colon | | SE_51081 | chr15:67466500-67469701 | Skeletal_Muscle | | SE_51874 | chr15:67467444-67469444 | Skeletal_Muscle_Myoblast | | SE_52344 | chr15:67466124-67469783 | Small_Intestine | | SE_63662 | chr15:67467303-67469755 | HSMM |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr15 | 67466980 | 67467913 | | chr15 | 67468171 | 67468380 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH15I067171 | chr15 | 67463621 | 67474069 |
|
Enhancer Sequence | GAGATGCAAA ATGAGATTTA AGAAGAGGCC TTGGATTTGG CATCAGGGTT TCAAGGGGGA 60
GCTTTTAGGG AGCAGTGTGT AGGAGGGGAG GGGCTGCAGT CAGTCAGCAG TGCACTGAAG 120
GGCAAGTACC AGGTGGGGAG GTGGAGGCAC CCAGCAGCGC AGCCTTTGTG CTGACTCACA 180
GTCAGTGCGT CCCAAACCCT AGGATGGAGG CAAGCACACA GGGAGCTCTT CCTAGGAAAA 240
AATGGGGACA TCTCAGGACA TCTGATTATT TCCTTTAAAG AGATTATTAT GAAATTACTG 300
TACAAAAAGA AAGAAAGCAG AGGACATCTG GTTTCTCCTT TCATTTCCTC CCCACTCCAG 360
GTGTTAGCCC CAGGGCTCAG GTCTGGGGAA GGTTGAGCCT CCTTGCCCCA GCAAAGCCAC 420
TTCTGGTAAG GGGCAGGGAC TCCTGGTTGA GACCTGGCTC AGCATCCTGC CCCAGGCAGG 480
CTCTCGGAGA CCCTGGGACC TGGGACCGTT GTTTGCAGGG CAGGAGATAT GAGCAGGTGA 540
TGTTCCTGTT ATTACACAGC GTGCTGGGTG AGTCACCGGG AATTTCCTAG GCATTTAAGG 600
CGGAAGGATT GGGGTAAATG GAGGGGAAGG AGGAGGCAGG TGGAGAGAGG AAAAAGGTAG 660
TGAGCTGGCT TCTGCCTGGT GAGTAAGTTG TTCCCTGCTT TAAAGTGAGA TGATTAGGGC 720
GGAGCCATGA CTGAGGAAAA TAATGTACCA GGGAGAGCCC TGAGGGAGCA GTTGAGCTGG 780
AGTTAAAGGA GGTGATGGCT TCCAGAGTGC CAGTGGCAGG AGTGAGAGGC AGGGATGGGG 840
CAGCTTGGAG TGAGAGGGAT AGGGCAGCTT GGAGGTGGCT GATGCCGGAT GCAGTGCTTC 900
AGACTGAAAG GTGGTCGTTT GCTGTGAATT GCCCTCTAGA TTGTGTAGAC TAGGATGATG 960
GGATGTTTCT TGAGCTTGGA CCCAAGGCAG CATCTCCTGT TGACATAGTT CTCCCTCCCT 1020
ACTGACGCTT CCTCAGGCAC CTTGCCTGAG AGTTGAGAAT TCTTAGGTTA TTTCTTCCAA 1080
AGGGAGGACC CTCCCCCCAG GGTGCCACTT TGCACTGGCC TAGTTGCACC TCTGCTGGGA 1140
AGGTGTGAAT CGGGGGCAAG TTGCCCCGTG AGTCAGGGTT AGGATTCTGG GTGAGACTCC 1200
ACGCTGACAG GCCCGGCTTC CCCTCTGCTT CATGAGCCCC TGTGCCCATG TGTGAGCACA 1260
GGTGTGGTGG CAGGGCGGCC CGAAGACCAC CAGCCCTGAG TGTGGACGGC GGCCCAGGGC 1320
AGAGGCCCAA CCCAGTTCCA GGCATCTTCA TGCTGCTGCC CAAGGCTCTT TTACAATGCA 1380
GCCTCTGGCT CCGGTCTTCC CCACACTTGT GAAATCACAG GCAGGGTCTT CCCCACACTT 1440
GTGAAATCAC AGGCAGGCAA CATAATGACA GGAAGTCAGC TGTCGGCTCT GTCTTCATAC 1500
TCCTGAGGGC CCGGTTTTTA GACTTTGCCA CTGTTCCTGG TTGCAGTATG CTGGTCATAA 1560
GCTAAAAGGG CATGGGGGTC TCTGTGCAGC TTGGTTTGGT ATTTTAGTCC GCAGATACAT 1620
AGGTTGGAAT TAGTACCCTG GGTGCTGGGA CACAGCTGGC GTGGGCTCAC AGAGACCTCA 1680
TCCTCTAGCA TAGGAGACTC AGGTACACAG TTTCTGGGAC ACAAGGTTAA TTCTGCACTG 1740
AGGCAGTGAG GGAGTGTTTC ACAGCCGTGT GAGCTGGGCC TTAAAGATCG AGTCCCTGCA 1800
GAGGAGGGGG ATGGGCAGTC CAGGCAGAGG ACCCAGGCAG GACTGAGAAG TGGTGGATGA 1860
GGAACATGGG AACTGGAGTG TGGAATCTCC TAGATTGAGG AAGAGCTGCC TTCCGCAGGT 1920
GAGGTGGGCC CAGCAGAAAC CAGCCCATTT CTGTTTTGAC CTTTCGTCTT GCAGCAGCAG 1980
TGCTCCTGGC CTTTGCCCGT TCCTTGCTTT CGATTTATAG GAGAAAGTTA ATTTCCCCCC 2040
TTGCCTCCCC ACCTCTTCCT TTACGGGATT TGAATCTCTT GCACATGTTT TTAATAGGCA 2100
TCCCTTAATC CAAGTGTTGC CTTCTGGGTT TTATTCTGTT TTCTTTTTCT TAAACATAAT 2160
GGAACGTCTG TGCCAGCTTG GAACAGGACT GAAAACTGAG GCCAGCCAAT GCGTTAGGCT 2220
GGCAGGGGGC CAGCCATGGA TTAAGTGCCC TATGGCACTT GAGAAGTCTG GCCGACACCA 2280
CACTGGTGGG GGAGGGGGAT CCACAAAGGC TGGAGCTGGA GGTTCCTGCG TCTCCAACAC 2340
CTCTGCACTG GGAGGAGAGA TTAGCACAGA CTCAGAAATC TGGCCAGGAG CAGGGCTGTT 2400
TGAAGGGAAG GCCGTGGGCA CGTGCCATCG TCTACCACCC CAGCTGTGCA AAATGCTCAG 2460
CCTAGAGGTG AAACTGCTCT TCAATGGGGT GTGTCACCTT ACCCCCCGTA GTCATTCTCC 2520
TAGAGGAGCC TTCTATAGAA CTGCTTCTGC ATTTGTTGGT AAATCCTTGA AACCAGATCT 2580
TAATTTGCTT GCTTGCTTGA TCAGTTGATT GATTGGTCAG GGGAGGGGTT GCCACCTCCC 2640
CCTGAGAGAT TTCTTTTAAG ATTTAATGCC AGGACAAACT TTGTTTTCCC TGAGGAACTA 2700
GTAAGCATTG CCCATCCACC AACCAGAGCC ATAGACCATG TCATGTTCCC TTTTTGTCTT 2760
GTCTACTAGG AAGCTCAGAG CCAAACTGGA TGCTTTTGCA GTAACTATAA CCTCATGGTT 2820
ATCCCATTTA TAGCCGCCTT CTTTCCAGAG TCCTTTTTGT 2860
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