| Tag | Content |
|---|
EnhancerAtlas ID | HS103-21096 |
Organism | Homo sapiens |
Tissue/cell | HUES64 |
Coordinate | chr6:39170520-39175120 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Klf1 | MA0493.1 | chr6:39171722-39171733 | AGGGTGTGGCT | - | 6.02 | | MAFF | MA0495.3 | chr6:39174270-39174285 | CTGCTGACTCATCAC | + | 6.22 | | MAFF | MA0495.3 | chr6:39174270-39174285 | CTGCTGACTCATCAC | - | 6.3 | | MAFG | MA0659.1 | chr6:39174267-39174288 | GAACTGCTGACTCATCACCTT | + | 6.56 | | MAFG | MA0659.1 | chr6:39174267-39174288 | GAACTGCTGACTCATCACCTT | - | 6.77 | | MAFK | MA0496.2 | chr6:39174268-39174287 | AACTGCTGACTCATCACCT | + | 6.68 | | MAFK | MA0496.2 | chr6:39174268-39174287 | AACTGCTGACTCATCACCT | - | 6.96 | | NFE2L1 | MA0089.2 | chr6:39174269-39174284 | ACTGCTGACTCATCA | - | 6.13 | | Nkx2-5(var.2) | MA0503.1 | chr6:39174211-39174222 | AGCCACTCAAG | + | 6.62 |
|
| | Number of super-enhancer constituents: 15 | ID | Coordinate | Tissue/cell |
| SE_23358 | chr6:39170147-39174537 | Colon_Crypt_1 | | SE_24296 | chr6:39170718-39171777 | Colon_Crypt_2 | | SE_24296 | chr6:39171815-39173834 | Colon_Crypt_2 | | SE_27719 | chr6:39168097-39179615 | Fetal_Intestine | | SE_28608 | chr6:39162941-39181506 | Fetal_Intestine_Large | | SE_31742 | chr6:39169517-39179450 | Gastric | | SE_40245 | chr6:39173560-39174995 | K562 | | SE_47837 | chr6:39171062-39171586 | Pancreas | | SE_47837 | chr6:39171645-39173836 | Pancreas | | SE_47837 | chr6:39173992-39175117 | Pancreas | | SE_50547 | chr6:39170538-39174766 | Sigmoid_Colon | | SE_52394 | chr6:39169209-39178848 | Small_Intestine | | SE_57304 | chr6:39169967-39171748 | VACO_400 | | SE_57304 | chr6:39171766-39174177 | VACO_400 | | SE_57620 | chr6:39170631-39173217 | VACO_503 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 3 | Chromosome | Start | End |
| chr6 | 39172491 | 39173096 | | chr6 | 39174410 | 39174631 | | chr6 | 39174931 | 39174988 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH06I039195 | chr6 | 39163284 | 39179611 |
|
Enhancer Sequence | TTGGCAGCAG GGCCTCTGCA GCTCAGGTTT AGCTCTATCT AGGAAGCCAC AGGGCCATCT 60
TCCAAATGCA GACCTGTGCT CATGGAAAAG GTGGAACCAA CCTGGATTTG AATCAGAGGG 120
GTCTCTCGAT GGCTGGCAGC AAGCCTCTGG GTAAATAACT CAGCCTCTCA GCCTTACTTT 180
CTCTGTCTGT AAAATAACAC CTACTCTGCA CACATGAAAA GAACCTAGGA CTCAGTAAGC 240
ACTGGATAAA TGTATCTGCA ATCAATATTG TGATTCACAC GTGTGTCCGT CAGGAACAAG 300
ACCCTGCAGA GATCTGAGAC CCAGGAGCAA AGCTGCTCAC CCCCAAAGCT GAAGCAGATG 360
GGCTGGCATG TCCTGGACAA GCAGTAGAGA AGGACTAGGG ATTTCAAGCC CTGTGCCTGG 420
AAGACAGGAA AGGGTGAGAA CACTGTCCCT AACCTTCTTC ACAACTGCCA ACTCTTCCCA 480
TTTCCCCATT TTAACAGAGA AAACTGTCGA TTTTCAGCCT GATCCATCAG CTCCCTCAGG 540
CCACATGGAG GAAGGGACTG TGGTTCCAGA GATGTTCCCT GGCCACCTGA TGGCTGGGAG 600
TCAGGGGCAG AGGGAAACGG GCAAGCCCAA GATGCCTCAC CCCATCCCTC AGAGGCCCCA 660
TCTCTCCTGG CCTCTGCCCC TCAGAGGCTC ACAGCCACCC TGGCCAGTTT CTCGTCCAAC 720
CAAGCAAGTT GGGCAGGGCT GCTGAGGGAA AGAAATGCCA CCACTGGTCC CATCCTGTCT 780
TCACCACTTC CCCCCCATCA CCCCTGGCAG CCGCCAGTAC CTCCCCAGGT GAGGCTGAGG 840
CCAGGAGGTG TTAGATGGCA GCTTCTCTGA ACTCTAGTCC AACTCCCTCC CAGCCCCCAC 900
CCAGCGTGAA CATGAAGCAA GACAATGGGC AGTGGCTCTC GGTACAGGCT GCCCAGTAGA 960
TCCCCTTGGA GGTTAAATAA ATGCTATGCC TGGTCCCCAA CTGCAGATAT TCTGTTGACC 1020
TGGCACAACT TTTAAAAAGC TCCAGAAGTG ATTCTAATAT GCAGGGGCTG CCCTAGTGGA 1080
AGCTGACAGG GGGAGGGAGG CTCAGGCCTT CTCCATCTTC CTGTCTAAAA AGGAGTATGC 1140
AGGGCAGAGA GAAGGAATTC TTGGTATTTT CCTCACTGCC TCTCCCCCCG GGTCAGGTGA 1200
CCAGGGTGTG GCTCGGAGGG CAGCTGTAGT TTACGAGCAA GGTATTGGCA AGGGCCCAGT 1260
GGTGCCACCC TGATACCTGC ACCAGCAGCC AACCCAGCTC GCCTGAGCTT TGTCTCTCCC 1320
AGGGAAGGAG CAGATACTGG ACGAAAGGCA GCAGGGCCAC ACCCGTCTCC TCGAAGACCA 1380
GAGCTGGGCT GTTGCAAAGC GGACTTTGTT AACTTGTGGT TGCTTATCTC TTTTCTCAGA 1440
TTTGCTCTGA TATCTATCTG GAGTATGGAT CACATTTGAG AAGAAGGCAG GCAGGCCAAA 1500
TCAATGGCTG GAGGCTTTGG TGTGCTAGGA CGTCGGCGCA GGGCCTAAAA ACCCAGGCTC 1560
AGCTCAGCTC TGCCAGTACT GTCTTGAGAT CCTCGAAGAA TCTTTGATTG CTTTGCCTGC 1620
CTGCTTCTCT GTACAATGAG GAGGTTGGAC TATGACTACT GGAGTCCCCC TGCCTGGGCA 1680
GGTGATACCT CCCCTACCTC CTCTCCATAG CACATTCAAG AAAATGCATT TCTATCCTCA 1740
GGACTTAGCT CATCAGTCAC CATACTACTT CTTAACCTGG ACTACAAACT GAGATCATCT 1800
GAGAGAGCTT GGAAAAATAC TCCTGCCCGG GTCCTGCCCC TAGAGATGCC AAGAGAAATA 1860
GTCTGGGGCT TGAACTGCGA ACCAGGATGC TGCAAAGCTC CCCCAGGTGA TTCTAATCTT 1920
ATGTTCAGCC AAGTTTCAAA CGCACTGCCC TAGATCCAAT CCATTCTCCC TCATTAGGGA 1980
CTTGAGCGCA GCCCCACCCC TGACATTAGC ACGGGGCAGG CTGTGCATGC ACACAGGCAG 2040
AACTGTCCTC TTGTCCACCT TTGGGCTTCC CCCAGCCTGC CCTCCTGGGC CATCTCTCAG 2100
CAGTCTCTGC AGAGCCCAGA GGCACTGCTA GGTCTCACGC TCAGGAGGGC AAGCCCCTGC 2160
CAGATGGGAG CAGGTTTTCA GCAGAAACCC TGGGCTTCTG ACTTTCACAG GCCTGGGAGC 2220
CCTGTCCTCA CTGGGAGGAA CAAAGAAAAC AAGGCAGGTG ACCCTGCCCG CATTGTTCTC 2280
AGGCTGGGAC GGTAATCCCC CAGGGCAGGG GGGCAGCTGG GCATCCCTCC TGTGAGAACA 2340
AGCCCAGGGC AGAGCTGACC TGAGGTTGCA GGTTTGGCTA AGGCAAGCAG TGAAGGGCTG 2400
GTGGGGCCCA AGCTCAGGAT GGAATGTCAG CGTGAGCTCT CAGGCACCTG GAGGGCTGAG 2460
CTGATCAGTG ACTGACACTG GAAATCCCTG TGCGGGCAGA CACAGGGGAC CTCGAGGGCC 2520
CCTTCCTGGT CCCACAGCAC TGCTGTGTGC CTGAGAAGTG GGCCTGGGGA GCAGGAAAGA 2580
GCCCCCTCCC TCTCAAACAC ACATACCAGA TGACCCTCTG AGGCCATGCT CTCAAAATCT 2640
ACCCCTGCCT CATCTTCTCA GGGAAGGTGG GATGTGTCCA GGGAGGCTTA AATGACAAGA 2700
GGGACATCCT TCATTTACCT ATAGCTTCTC TACCCCAATT CACAACCACT GCCCTGCCCA 2760
GGGTGGCTAT GGCCCAGGTC CATGGTCCTG TGCTGGTGTC TCTGCCCTAT CTGGGACACT 2820
GAGGCCTGGA TTTGTGACTT TGTCCCCTTC TCTGCCCCCA GAGTTCAGAT CCCAGGGGTG 2880
TCTGACACCT CTCTGCCCTG AGCGATGCCA AGGGGTGTCT CCCAATTAGT GGGACAACAG 2940
TGTCAGTAGG GACAGGAAAC AGTTTTAGCT GGGATCCCTT GAGCCTGTCC AGCTGGGCAG 3000
AGCAGCCTCC TCCATTCCTC CATAAGGCTG TGGGTCACTA GGAAGAGGCC TTACTTCTAA 3060
GGTGGGGTTA GAGAGCTCTA GCCCAAGCCC CTGCACTTGG ATTGGGCCCC TGGCACATTG 3120
TCCTTTCCAG GGAAGCCAGC AGTGCTCTCA GGCCTGGCTC ATTCCTCCCC GACTTGGTTA 3180
ATAAGGGCCT GAGTTAGCAT TTCCCCACCA AAACCCCACA TTCATCAAGC ACCTCTCACA 3240
CCCATAACTC CTCTTCCACC GTCTAATCTG AGACCTAAGA CCCTGAAGGG AAACCAGACA 3300
AAATGGATAC ACTATTCCCA TTCTGTAGAT GAGGAATCTA TAGAGAGGCT AGAAAGATGG 3360
TGAAGCCAAA CAGAAAGATG GTGAAGCCAA ACAGCAAGCT GGTGACCCAG CAGAGCAGGT 3420
GAGGCCCTGT CCACAGAACA ACCAGCCCTC CACTTGCCAC CCGGAACTGG GCTGAGAAAC 3480
ACCAACCAAA GCACAGCAGG GAATGTGCAG GTAGACACTG GTGACATAGC AGAGATAAAG 3540
GGCTGTGCTG TGCGGTCATA CCCACGGATC TGACCTGACT ATATGAGTTA GGGTAAGCGC 3600
GTGCCTACGC TCCCTACCCC ATTCCCCTGC AGATGCCTCA GATTTACCTT GACCTTGGGG 3660
TGGGGTCAAG GATCAGCTAC AGGAAGCCAC CAGCCACTCA AGGTTTCTAA AAACAGTCCT 3720
TGGAGCAGGC CAGAAAGGTG GCTGTGGGAA CTGCTGACTC ATCACCTTCC CATCCCGGGC 3780
CAATGACCTG AGGGAGGTGC AGTTCCCGGG CCGCCCAGCT GCCCCTCGCG TGCTGGCCTG 3840
CTTCCTGTCC TCCCAAACCC AGCTCTGCAC TGGCACACAA GCTGGGCTGG CCAGTCTCTC 3900
CAACACAAAT ATCAAGTGTG GGGCCCTCTC TGAGCAGCAC AGGGGAGAGG GCAGAGGGGA 3960
AAGGCCACAT CTGGGTTCAA AATCCTGACT CCAGCATCCA CTAGCGGGTT ACCTGGGGCA 4020
TGTCTTATCA CCTCTCTGAG CTTAACACTC CGTATCTGGA AAACAAGAGT CATGGCTTCA 4080
CTGTGTTGGC GCGTCGATTA CAAAAAAATG ATGAACAGCT CAGTGCTGGG CACATGGGGC 4140
GTGTTCCAGA AACGAGCACT GGGAAGGAAA ATAAATGTGA CTATTATTGC TCTGTGAATA 4200
GAACAAGGGG CTTGGGGAGG ACACCTCCAT TCTGAGGGTC TGTGTCTGCT GCATGTGGCC 4260
TCCAGAGCTG GGGAGCTGGG CTAGGTGTTG ACAGCAATGC CCTCCTTCCA TTTACCACCT 4320
CCTGGGCATG GGCCAGTCCC TCCGGCTCAG CAGTTCACCC CCCTGTGCCT TTGCAGGTGC 4380
CTTCCTGCAG CTCACTCTTA CTTCAATCAG GTTTCACCTG AATGTCCCCT CCTGAAAGAG 4440
GCCATGCCAC CTGGAATATT AAGCCTCCGT CCCGCTCCCG CTCCTCACCT CACTGCACTC 4500
ATCACTACCT GACATTCTAC TAGGCATCTG TTTCTCTGGC TTCCTAGTTA TCTACCCTAA 4560
ATAGATCATG AGCCCTACAA GGAGAGACTC ATGGATCCCT 4600
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