EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS078-10910 
Organism
Homo sapiens 
Tissue/cell
H2171 
Coordinate
chr20:48982530-48984270 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs6067417chr2048983697hg19
TF binding sites/motifs
Number: 24             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EWSR1-FLI1MA0149.1chr20:48983073-48983091CCTTCCTTCCTTCCTTCC-10.83
EWSR1-FLI1MA0149.1chr20:48983077-48983095CCTTCCTTCCTTCCTTCC-10.83
EWSR1-FLI1MA0149.1chr20:48983081-48983099CCTTCCTTCCTTCCTTCC-10.83
EWSR1-FLI1MA0149.1chr20:48983061-48983079CCTCCCTCCCTCCCTTCC-7.08
EWSR1-FLI1MA0149.1chr20:48983043-48983061CCCTCCCTCCCTCCTTCC-7.12
EWSR1-FLI1MA0149.1chr20:48983085-48983103CCTTCCTTCCTTCCTTTT-7.95
EWSR1-FLI1MA0149.1chr20:48983065-48983083CCTCCCTCCCTTCCTTCC-8.13
EWSR1-FLI1MA0149.1chr20:48983069-48983087CCTCCCTTCCTTCCTTCC-9.42
IRF1MA0050.2chr20:48983319-48983340ACACAGTTTCATTTTCACCTT+6.64
MyogMA0500.1chr20:48984003-48984014GACAGCTGCTG+6.14
Stat6MA0520.1chr20:48983524-48983539GTTTTCCAGAGAAAA+6.07
Tcf12MA0521.1chr20:48984003-48984014GACAGCTGCTG+6.02
ZNF263MA0528.1chr20:48983056-48983077CTTCCCCTCCCTCCCTCCCTT-6.14
ZNF263MA0528.1chr20:48983081-48983102CCTTCCTTCCTTCCTTCCTTT-6.16
ZNF263MA0528.1chr20:48983043-48983064CCCTCCCTCCCTCCTTCCCCT-6.46
ZNF263MA0528.1chr20:48983042-48983063TCCCTCCCTCCCTCCTTCCCC-6.61
ZNF263MA0528.1chr20:48983069-48983090CCTCCCTTCCTTCCTTCCTTC-6.76
ZNF263MA0528.1chr20:48983073-48983094CCTTCCTTCCTTCCTTCCTTC-6.94
ZNF263MA0528.1chr20:48983077-48983098CCTTCCTTCCTTCCTTCCTTC-6.94
ZNF263MA0528.1chr20:48983039-48983060GTCTCCCTCCCTCCCTCCTTC-7.12
ZNF263MA0528.1chr20:48983065-48983086CCTCCCTCCCTTCCTTCCTTC-7.19
ZNF263MA0528.1chr20:48983061-48983082CCTCCCTCCCTCCCTTCCTTC-7.38
ZNF263MA0528.1chr20:48983052-48983073CCTCCTTCCCCTCCCTCCCTC-7.65
ZNF263MA0528.1chr20:48983048-48983069CCTCCCTCCTTCCCCTCCCTC-7.73
Number of super-enhancer constituents: 6             
IDCoordinateTissue/cell
SE_28491chr20:48982335-48987321Fetal_Intestine
SE_31629chr20:48983043-48983874Gastric
SE_33764chr20:48982789-48984100HCC1954
SE_52401chr20:48982681-48987083Small_Intestine
SE_53316chr20:48982599-48984069Spleen
SE_56118chr20:48982851-48984157u87
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr204898308348983800
Number: 1             
IDChromosomeStartEnd
GH20I050365chr204898243148987174
Enhancer Sequence
GAATCCCCAT TATCCCATAC TCTGCAACAC TGAGAGTTGC CAATCTTTTT TGTCTTTTCT 60
AATCTGATAG GCAGAAAATG ACATATCATT GTAGCTTATC ATTGATAACT GGTGGGGTGG 120
AACTTGTCTT CATACTTTTT TTTCTTTTTT TCTGAGGCAG TGTCTCCCTT TGTCTCCCAG 180
GCTGGAGTGC AGTGGCACCA TCTCAGCTCC TACATCAGCC TCCCAAGTAG CTGGGACTAC 240
AGGCATATGC CACCACACCT GTCTAATTTT CCTTATTTTT TGTAGAGATG AGATCTTTCT 300
GTGTTACCCA GGCTGGTCTT AAACTCCTGG GCTCAAGCAA TCCTTCCACC TCGGCCTCCC 360
AAAGTGCTGG GATTATAGGC ATGAGCTGCC TCGCCTGCCA GAATAGTGGG TTTTTAATAC 420
GGTGTTTACC TCTTCTTATT GTTTTGCAAG AACTCTTTGT ATATTAAGGA TAGTAATTCT 480
TTCTAAGAGT CTTATAATTG ACTATAAAAG TCTCCCTCCC TCCCTCCTTC CCCTCCCTCC 540
CTCCCTTCCT TCCTTCCTTC CTTCCTTCCT TTTGTTCCCT TCTGCTTTCT AAGGATATGC 600
CTGGTGTTTG GCAAGCATTG CATGAATTAC ATTAGGAAAT AACTTTTGTA ACAAACCCAT 660
TTAACAACCA TTCTTTGTTC CCCGCCTCCT GATAATGCTC AGAGCCACAG CAACAGCCTT 720
TGCCCAACTC CATGTCATTA ACCCTTGATC TTTTCCTGCT GAATAGCAGA TTGCTTTCCG 780
GGGCTGGCAA CACAGTTTCA TTTTCACCTT CCTGCTGATG GAACTGCCCT GGCTCTGTGC 840
CAGATGGCTG TTTACATAAG AAATGATTTG ATTATATTGC ACAGCCAATG GCAGCCTTTC 900
TCAGAATAAA GAAGCCAGAA ACATATAATC AAAGCCATTA ACTGTGTACA AAGAAACGCA 960
GCCCACTCTA AATTTCCCAC CAACCATAAT CACAGTTTTC CAGAGAAAAA TAAGAACAGG 1020
GTTATGGTTC CCTACTAAAA ACGTGTTAGG GGAAAGACTT TTAAAAGGAA ATTGTGGTAT 1080
AGCTCAGTTG CACTCTCAGA TCAACCCTTG AGCCTTGACT CCAATCCCAG CTCTGTAACT 1140
CACTGTCCTT GTGACCTTGG AAAAGTCGTT TACTGCCAAA AGCCTCCGTT TCTTTATTGT 1200
AAAATGGCTA TAATAGTAAT ATCAACCTCA GAGGTTTACG AGAGGATTAA GTGAGATAGT 1260
GCATAAGAAC ACTTTCTCAG TCAGAATGTT TTCAGCCGCA AGGAGCAGAA CACTTGACTA 1320
AAGGAGGGAA AAAAAAGCTA GAGGACTTAT AATTTTATTT AACAGGGTTG TTTCATTTGG 1380
AGGCATAAAG ATGTAACCAG TGATTCACAT TCTTTTCTTC TTCCTGCTAT GCCATTCTCA 1440
GCAATTTATG GACATGTCTC CTCATGGTTT CAAGACAGCT GCTGTGGCTC CAGGCATCAC 1500
ACTGGGACAT GATAAAATCA AGCAAAGAGG AGGAGGGCAT TTTTTCCCCT GTGTCTCCTT 1560
TCATGATGGA GAAAATTGTT CCCAAATTTC CCCCCTGCAG ATCTGCAGAC TTCTTATTGG 1620
CCAAGATGGC GTTACATCTA TAATTCCAAA CCAGTCACTG ATGGAGGAAT GAGAATGACT 1680
GCAGTTGGCT TGGACCTATA ACTCACTCTG AAGCCGGGGC GAGGAATAGC CACCGTCCCT 1740