| Tag | Content |
|---|
EnhancerAtlas ID | HS187-08534 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr15:67466580-67469460 |
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 | CTTCTGTCTT ACCGCCCCAT TACCCATCCA TAGATCTGAC TCTGGAAACA CCGATGAAGT 60
TTGGCTGAAG TCATGCCAGT GGATGGATTT AGTGGAGAGG CCGACCCAGC TCAAGATGGA 120
AAGACAGCCA GAGATGCGCT CGGGTGGTGG GGGTTCCTTG GAGAAGGCTG AGGTCAGGGG 180
GATGATGGGG TCACAGCAGC TCAGAGGGGA GGCAAGCCCT GAAGGACAGT GGCTACAAGC 240
GGGCCCTGCA GAGATGCAAA ATGAGATTTA AGAAGAGGCC TTGGATTTGG CATCAGGGTT 300
TCAAGGGGGA GCTTTTAGGG AGCAGTGTGT AGGAGGGGAG GGGCTGCAGT CAGTCAGCAG 360
TGCACTGAAG GGCAAGTACC AGGTGGGGAG GTGGAGGCAC CCAGCAGCGC AGCCTTTGTG 420
CTGACTCACA GTCAGTGCGT CCCAAACCCT AGGATGGAGG CAAGCACACA GGGAGCTCTT 480
CCTAGGAAAA AATGGGGACA TCTCAGGACA TCTGATTATT TCCTTTAAAG AGATTATTAT 540
GAAATTACTG TACAAAAAGA AAGAAAGCAG AGGACATCTG GTTTCTCCTT TCATTTCCTC 600
CCCACTCCAG GTGTTAGCCC CAGGGCTCAG GTCTGGGGAA GGTTGAGCCT CCTTGCCCCA 660
GCAAAGCCAC TTCTGGTAAG GGGCAGGGAC TCCTGGTTGA GACCTGGCTC AGCATCCTGC 720
CCCAGGCAGG CTCTCGGAGA CCCTGGGACC TGGGACCGTT GTTTGCAGGG CAGGAGATAT 780
GAGCAGGTGA TGTTCCTGTT ATTACACAGC GTGCTGGGTG AGTCACCGGG AATTTCCTAG 840
GCATTTAAGG CGGAAGGATT GGGGTAAATG GAGGGGAAGG AGGAGGCAGG TGGAGAGAGG 900
AAAAAGGTAG TGAGCTGGCT TCTGCCTGGT GAGTAAGTTG TTCCCTGCTT TAAAGTGAGA 960
TGATTAGGGC GGAGCCATGA CTGAGGAAAA TAATGTACCA GGGAGAGCCC TGAGGGAGCA 1020
GTTGAGCTGG AGTTAAAGGA GGTGATGGCT TCCAGAGTGC CAGTGGCAGG AGTGAGAGGC 1080
AGGGATGGGG CAGCTTGGAG TGAGAGGGAT AGGGCAGCTT GGAGGTGGCT GATGCCGGAT 1140
GCAGTGCTTC AGACTGAAAG GTGGTCGTTT GCTGTGAATT GCCCTCTAGA TTGTGTAGAC 1200
TAGGATGATG GGATGTTTCT TGAGCTTGGA CCCAAGGCAG CATCTCCTGT TGACATAGTT 1260
CTCCCTCCCT ACTGACGCTT CCTCAGGCAC CTTGCCTGAG AGTTGAGAAT TCTTAGGTTA 1320
TTTCTTCCAA AGGGAGGACC CTCCCCCCAG GGTGCCACTT TGCACTGGCC TAGTTGCACC 1380
TCTGCTGGGA AGGTGTGAAT CGGGGGCAAG TTGCCCCGTG AGTCAGGGTT AGGATTCTGG 1440
GTGAGACTCC ACGCTGACAG GCCCGGCTTC CCCTCTGCTT CATGAGCCCC TGTGCCCATG 1500
TGTGAGCACA GGTGTGGTGG CAGGGCGGCC CGAAGACCAC CAGCCCTGAG TGTGGACGGC 1560
GGCCCAGGGC AGAGGCCCAA CCCAGTTCCA GGCATCTTCA TGCTGCTGCC CAAGGCTCTT 1620
TTACAATGCA GCCTCTGGCT CCGGTCTTCC CCACACTTGT GAAATCACAG GCAGGGTCTT 1680
CCCCACACTT GTGAAATCAC AGGCAGGCAA CATAATGACA GGAAGTCAGC TGTCGGCTCT 1740
GTCTTCATAC TCCTGAGGGC CCGGTTTTTA GACTTTGCCA CTGTTCCTGG TTGCAGTATG 1800
CTGGTCATAA GCTAAAAGGG CATGGGGGTC TCTGTGCAGC TTGGTTTGGT ATTTTAGTCC 1860
GCAGATACAT AGGTTGGAAT TAGTACCCTG GGTGCTGGGA CACAGCTGGC GTGGGCTCAC 1920
AGAGACCTCA TCCTCTAGCA TAGGAGACTC AGGTACACAG TTTCTGGGAC ACAAGGTTAA 1980
TTCTGCACTG AGGCAGTGAG GGAGTGTTTC ACAGCCGTGT GAGCTGGGCC TTAAAGATCG 2040
AGTCCCTGCA GAGGAGGGGG ATGGGCAGTC CAGGCAGAGG ACCCAGGCAG GACTGAGAAG 2100
TGGTGGATGA GGAACATGGG AACTGGAGTG TGGAATCTCC TAGATTGAGG AAGAGCTGCC 2160
TTCCGCAGGT GAGGTGGGCC CAGCAGAAAC CAGCCCATTT CTGTTTTGAC CTTTCGTCTT 2220
GCAGCAGCAG TGCTCCTGGC CTTTGCCCGT TCCTTGCTTT CGATTTATAG GAGAAAGTTA 2280
ATTTCCCCCC TTGCCTCCCC ACCTCTTCCT TTACGGGATT TGAATCTCTT GCACATGTTT 2340
TTAATAGGCA TCCCTTAATC CAAGTGTTGC CTTCTGGGTT TTATTCTGTT TTCTTTTTCT 2400
TAAACATAAT GGAACGTCTG TGCCAGCTTG GAACAGGACT GAAAACTGAG GCCAGCCAAT 2460
GCGTTAGGCT GGCAGGGGGC CAGCCATGGA TTAAGTGCCC TATGGCACTT GAGAAGTCTG 2520
GCCGACACCA CACTGGTGGG GGAGGGGGAT CCACAAAGGC TGGAGCTGGA GGTTCCTGCG 2580
TCTCCAACAC CTCTGCACTG GGAGGAGAGA TTAGCACAGA CTCAGAAATC TGGCCAGGAG 2640
CAGGGCTGTT TGAAGGGAAG GCCGTGGGCA CGTGCCATCG TCTACCACCC CAGCTGTGCA 2700
AAATGCTCAG CCTAGAGGTG AAACTGCTCT TCAATGGGGT GTGTCACCTT ACCCCCCGTA 2760
GTCATTCTCC TAGAGGAGCC TTCTATAGAA CTGCTTCTGC ATTTGTTGGT AAATCCTTGA 2820
AACCAGATCT TAATTTGCTT GCTTGCTTGA TCAGTTGATT GATTGGTCAG GGGAGGGGTT 2880
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