| Tag | Content |
|---|
EnhancerAtlas ID | HS176-16007 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH |
Coordinate | chr17:17733170-17736070 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NR2C2 | MA0504.1 | chr17:17734081-17734096 | TGACCTCTCACCCCT | - | 7.11 | | RARA(var.2) | MA0730.1 | chr17:17735322-17735339 | TGACCCCTCTGTGACCC | - | 6.56 | | STAT3 | MA0144.2 | chr17:17734756-17734767 | TTTCTGGGAAG | + | 6.02 | | Zfx | MA0146.2 | chr17:17735994-17736008 | GAGGCCGAGGCGGG | - | 6.01 |
|
| | Number of super-enhancer constituents: 23 | ID | Coordinate | Tissue/cell |
| SE_00881 | chr17:17733709-17736055 | Adrenal_Gland | | SE_03206 | chr17:17734153-17735363 | Brain_Angular_Gyrus | | SE_23173 | chr17:17733254-17735884 | Colon_Crypt_1 | | SE_23799 | chr17:17733760-17734475 | Colon_Crypt_2 | | SE_23799 | chr17:17734505-17734839 | Colon_Crypt_2 | | SE_24725 | chr17:17733591-17735526 | Colon_Crypt_3 | | SE_26625 | chr17:17734078-17735937 | Esophagus | | SE_27885 | chr17:17733606-17735670 | Fetal_Intestine | | SE_28899 | chr17:17733505-17735994 | Fetal_Intestine_Large | | SE_31441 | chr17:17732630-17735538 | Gastric | | SE_31441 | chr17:17735560-17736033 | Gastric | | SE_34262 | chr17:17732622-17736139 | HCT-116 | | SE_42125 | chr17:17733834-17736003 | Lung | | SE_48150 | chr17:17733490-17736067 | Psoas_Muscle | | SE_50203 | chr17:17733573-17735794 | Sigmoid_Colon | | SE_51164 | chr17:17733014-17735923 | Skeletal_Muscle | | SE_52449 | chr17:17733481-17735613 | Small_Intestine | | SE_54926 | chr17:17733681-17736164 | Stomach_Smooth_Muscle | | SE_57042 | chr17:17733954-17734505 | VACO_400 | | SE_60863 | chr17:17723038-17753684 | DHL6 | | SE_61850 | chr17:17725940-17761172 | Toledo | | SE_62888 | chr17:17723024-17755643 | Tonsil | | SE_63332 | chr17:17727040-17744985 | NCI-H82 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 3 | Chromosome | Start | End |
| chr17 | 17734497 | 17735559 | | chr17 | 17733798 | 17733893 | | chr17 | 17733800 | 17734600 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH17I017829 | chr17 | 17732748 | 17735882 |
|
Enhancer Sequence | CTTGAACTCC CAGACTCAAG CGATCCCCCT GCCTCAGCCT CCCAAAGTGC TGGGATTACA 60
GGCGTGAGCC ACTGTGCCCA GCATCAATTA TCTTCCATGG AAGCCAAGGA TAGGGTGCTT 120
GTTCCCCATG GCGGGGGGTG CTCCCCACTG GCCTAGTCAG CCCCATCCTG TCTCTCACCA 180
ACTCCAGACC ACCACATGGT AGATGCTCAG AACTTGGAAC CATAGCCTGG TACATCCTAG 240
AAACTTCCAG CACAGGCTCC TTGGGTAATT GCTGCTAACA TTTGTTGAGC TAAACCTATC 300
GCGTGCCAGG TACTGGTTAG GTGCTCTAAA TGGTGATTTG TTTGTTTTCT CTAAAACAAA 360
CAGGGCCTTG CTATGTTGCC CAGGCTGGTC TTGAACTCCT GGTCTCAAGC AATCCTCCAA 420
CCTCAGCCTC TAAAGTCAAT AAGATTATAG GCGTGAGCCA CTGCATCTGG CTAAATGGTG 480
ATAATAATAA CACTAACTGG CATTGGTTCA GGGCCTACTA TGTGCCATGC ACTGCTTAAG 540
CCTTCACTCA TCGGATCCCC ACAATTCCAA GAAGCTGCTT TTAGTACTGC TCCCTTTACA 600
TTGTTAAGAA CCTGAAGGTT CTTGGACTTG TCCAAGGTCA TACAGTAGGG CTGCTTGTTA 660
AGACCCCTGA TCCCAGCCTT CTAGCTGCAG GGAGCACAGG GACCCCAGAG CCTGGCAGGG 720
GCAGCATGCA GAGGCAAGGC CTGCTGGGAG ACAGGTGCAG GGACGGGGAG TCAGTTAGGA 780
AAGGAGCTCA AACAGGGTTC GGGGTAGGCC ACAAATTCCC CCTAGGGGGA TGGACCCCCA 840
GCCCCGTCCC ACCTCCCACA AGCCCCAACC CAGCAGGGGA CCCACACCTG GAGCCAGTCT 900
CAATGGCTCC CTGACCTCTC ACCCCTGAGC CAGTTAAGGC TTTCCCCACC TCACCCCCGA 960
CACACACAGC CGCCCCTGTG GAGCACATGG TGCAGGCTGT CACACACTGT CAGTGCCCAG 1020
GGTCAAAAGG CATGTCCACA TGGCCCGTGG CTGCTAGGAG ACAAGGTCAG AGGCACTTCC 1080
TCTGGCCGGC CTGGGCTCCA CCTGTCAGCA GGCAAAGTCC AGATCCCAGG CCTCTGCTGG 1140
CAGTGACTCC TGCCTGGAGC TGACCGGGTC ACTCAGGATG TTTGTGTCCA GCTAGGTGAA 1200
TGTTGGGCAG AAGGTAACTC CCAACCCGGC TGAGACAAGG GAACTTTATC TTGGAGCACT 1260
AGGGAGCCAT GAATGGTTGG AGACCAGGGG AGTTCTGTGC TGTAAGCTAG GGCAGTAACT 1320
AGTCTAGAGC TGTGTTTTCT AAGGAGTGCC AGTGCTTGGT GGAACTAGGG AGAGAACTGG 1380
GGCATGAGAT ATCCTGGGGA GAGGTATGGG GTGGCAGAGC GGGCCCCCAT TGTGCCCTAC 1440
CAGGGCTGGC CTGGACCCAG CAAACAGCCA GACACATGAC TAGAAGCAAG GCCCTGTTGT 1500
GGCTGGGCTG GGCATGCTGG GAGGGACATC AGGGCGGGAG AACTCTGAGA ACGCACTGCT 1560
CGGGGCAAGG TGACACCCAG AAGGGCTTTC TGGGAAGCAG CCTCTGACGG GGCTTGGCAG 1620
ACATCTGGGG TCCGACAGAC AAAGAGCAGA CATGACGGGG TCCAGGCATA GGAAAGAGAC 1680
CCCGAGGCCC TGTTCCAGGC TCTTGGCCAG AACTCTGTTT CCGTCTGCCT CTTCTGCACT 1740
CATAAGCTTG TGCAAAATTG GATAAATTAA TCCTCAGCAG GGAGGTGAAG ACTGCCACGG 1800
GCTTAACAAT AATCCCCAAC ACAGGTACAG GGCCATCTCC TGATCCATCC TCCCCCGACA 1860
GCTGCAAGGT ACTCTGAGGC CCAGAAGGAG ACAGGCTCAC CTGAGGTCTT GGTGCAGATG 1920
CAGGACTCAA ACCCAGGGAC ACTATAGCCA GGGCAGTGCC TTCACCCACA GATGCAAGGA 1980
CTCATGGAGG CAGCTCCATC CCCAAATCCA TTCACATGAC AAGAGTTTGG CTGTGGCAGG 2040
CAGCAGGACC GGATGGGGCC CAAGGCCCTT GGCTGGCTCA CCAGGGCTGG TTCCCAGTCT 2100
AATGACTCAA ACACTGCTCT GGACTGGGAT GGGGAGGTAG CCACATAGCC TCTGACCCCT 2160
CTGTGACCCA CTTCCAGGCC CCCAGAGTAG CCCCTGTGGA GGAGCCTCCC TCAACCCCTC 2220
ATCCCCATTC TTAGGAGCCC AGTGCTTAAG AGCTTAAGAG CTAGGCTCTG GAGCCCACAG 2280
CCTGGGTTTG AATTCTGGCT TTGCCATCAT CTGGCTGTGT GATCTCAGGC AAATCACTTA 2340
ACCTCTCTGG TCCTCAAGGC CGTCATCTTC ATCATATGTC TACCTACTTG GGGTTGTCAG 2400
GGGATTAAGT GGGATTATCA ACACACTGTC TGAAACACAG TAAGTACTCA ATTAGTGTTT 2460
TCTGTTCACA TTACGATCCT CCATCCAAGC AGCCAGAGGG AACTGAAGCT CGGTGTGCCC 2520
CTGCTCTGAC CCCCGACTGT CCTCACATCT AGCCCAGCTC TGCACTCTGG CACTCAAGGC 2580
CAGCCTGGCC CCCTCTTATC CCTCATGTCT CTCAAGGGAC CTGGCATTTC CACCCCCAAA 2640
TCTTCAGACC TTATCAAACC TGCTCAGCTC CACTCCTGGT AGAAGAAGCT TCAAAAGCAG 2700
GCTCGACCTC TGACCAGCAA TTCCCCTCCC AGAACCTCAT CCTAGGAACA CAGTGAGGAT 2760
CCGGGCAAAG ACTGGCCTCA GTGGCCAGGC ACAGTGGCTC ACGCCTGTAA TCCCAGCACT 2820
TTGGGAGGCC GAGGCGGGCA GATCATGAGG TCAGGAGATC GAGACCATCC TGGCTAACAC 2880
GGTGAAACCC CGTCTCTACT 2900
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