EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS176-12754 
Organism
Homo sapiens 
Tissue/cell
SK-N-SH 
Coordinate
chr14:69148930-69151080 
SNPs
Number: 2             
IDChromosomePositionGenome Version
rs4902632chr1469149428hg19
rs10144968chr1469150885hg19
TF binding sites/motifs
Number: 3             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
NEUROG2MA0669.1chr14:69149432-69149442GACATATGTT-6.02
Stat6MA0520.1chr14:69149123-69149138AGTTCTCTGGAAAGC-6.37
ZNF263MA0528.1chr14:69149384-69149405CCATCCTGCTCCCCTTCCCCC-6.03
Number of super-enhancer constituents: 32             
IDCoordinateTissue/cell
SE_03035chr14:69149829-69150429Bladder
SE_09837chr14:69145943-69153774CD14
SE_10804chr14:69147805-69153516CD19_Primary
SE_11797chr14:69147184-69154238CD20
SE_25846chr14:69147216-69151396Duodenum_Smooth_Muscle
SE_26618chr14:69147082-69150870Esophagus
SE_27779chr14:69147782-69150672Fetal_Intestine
SE_27779chr14:69150857-69154054Fetal_Intestine
SE_28733chr14:69142983-69154144Fetal_Intestine_Large
SE_29577chr14:69146058-69153767Fetal_Muscle
SE_31476chr14:69149177-69149668Gastric
SE_31476chr14:69149776-69150715Gastric
SE_36049chr14:69148571-69151003HMEC
SE_36916chr14:69146511-69158224HSMMtube
SE_40886chr14:69147194-69149654Left_Ventricle
SE_40886chr14:69149746-69152857Left_Ventricle
SE_42158chr14:69147179-69151806Lung
SE_44336chr14:69146331-69154085NHDF-Ad
SE_46756chr14:69149870-69150688Ovary
SE_48603chr14:69147190-69151762Right_Atrium
SE_50095chr14:69147189-69153363Sigmoid_Colon
SE_51137chr14:69146762-69151267Skeletal_Muscle
SE_51770chr14:69147182-69154099Skeletal_Muscle_Myoblast
SE_52662chr14:69147197-69153302Small_Intestine
SE_54587chr14:69148740-69150722Stomach_Smooth_Muscle
SE_55866chr14:69148008-69153685u87
SE_60240chr14:69134391-69156849Ly4
SE_62911chr14:69129549-69162790Tonsil
SE_63560chr14:69147182-69157806HSMM
SE_65119chr14:69148699-69149696NHEK
SE_65119chr14:69149700-69150601NHEK
SE_67722chr14:69148008-69153685u87
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr146914915569149350
Number: 1             
IDChromosomeStartEnd
GH14I068679chr146914590169157990
Enhancer Sequence
AAACCCATCG CCTGGCCACA AGTCTGGTGC CCTATCTACA CCAATCTGTC TCCGGTAAAC 60
CTAACTAGCT AGTCAACTTT TCCCATCCAT AGGCCAGACA CCTTTTGAAA TAACAAACCA 120
TCTGATCTCT AGAAAAACTG AAAGGCCAGT TCCAGTTGTC AGACACACCA AGCTCGAGAG 180
AGTCTCTCCC AAAAGTTCTC TGGAAAGCCC AGGGATTCCG AATTCCAAAG CCAGCCAAAT 240
TTGAATTTCC TCTATAAAGA GATAGTCCCT CCTGGTTTAG AACATAACCT TCCTCATTAG 300
GCTGGTTCCA TGTTTTGTAA TAACTTTTGC TTACACCACA AAATTGTCAT AGATTACGAA 360
AACACAAAGG CCTTGGAAAA AAGGCCCAGA GCCCCCTGGA AGTCATTATT TCTTCCTTTA 420
GCAATTGCTG AGTTAAGCAC CATAAATATG GTTCCCATCC TGCTCCCCTT CCCCCGCCCT 480
CCCCGCCCCC CACGATCAGC TGGACATATG TTAGGAAGAA AGCAGGGACG TGGGGGTGGA 540
AGAAGATTCG CATGTCGTGA ATCTTGAGCA CTGAAAAGAA AAAGTGGGGA GAGGGCGGGG 600
AGTTTGCAGC CCTGGAAATG GAATCTCTGA AGGATTTATT GCCTTTGAGT ATCTCACAAG 660
GCTTTTTTTT TTTTAATAAA AATCTGTAGC TTATGGCTTT TTTTTTTTTT TTTTTTTGTA 720
TAGGGCAGTA AACAAGAGCT CTGAAAGGGG AAGGAAGCCA GGAGAAAGCC AGCTCCATTA 780
GTCACGCAGC AGCATATCCT GTCACAAAGG ACCCCAGTTG AGTAATCGCC CAAAATATGC 840
CTGTTATTTT TTTCTGTCAG AAAAAAAATG GGGCCTGCCA AAACGTACTG TAAAAAAAAA 900
AAAAATCTGG TGTCTTAGGC CCAGAGAGGG AAAAGAAAAT AAAGAAGAAA GAGTCATAAT 960
TTCACAGTGC TCTTCAAACC CTCTCCCCAG CTTACCTGGA AAAGAAAAAG CCTTCAGACT 1020
CTTCACCACG ACAGAGCCTG CCAGGCTTGA AGAAAGCTAC AGCCTTGGGA TGGTCCAGTT 1080
CTCAGAGTCT TCATAGTTAC TTGGTGCCAA GAGCTTAAAA AGAGGAGGGG TGGTCGGGGA 1140
AAGTTGAAGG AGGACAGCAC GGGGGGAGAG AAAAAATGAA CAGAAAGGGA CCCAGGATAT 1200
TGAACAAGTC CTTTGACGAG CTTTAAATGG GTGAGGCATT GCTCATAGGG AACCCGCAGG 1260
AGCCCACACC AGTTCCATGA GTATTGCATG AGCCCAGCAG GGGCTAGTGA CTTCCAGCCA 1320
ATGGCCGAGC CTGCTTCGTA AGCTTTTCTG ATGGCCCCAG CAAAACCAGC ACTGTCTCAG 1380
GCCTCCACCA TGCCCTGTGG GTGTTTGGGC CACAGACTGG ACAACAAGGA CTTGTGCAGA 1440
AGGACATCGG ACTCTGGAGA GGTCTGAAAC AAGGGGTGGG GAGAGACAGG CTGGTCAGAG 1500
CTGCCTGCAA CCTCCCGTAT TCTCCTGGAT TGGCCTTCCA AAACCCGGGC TGACAGGCTC 1560
TTGGTAGGAA AACAGGCCCA GCAAACAAAG GTGTTCTCAA GCCCAGTTCA GTCACTGCCT 1620
CTGTCCCATG CTCTTAGTCT CATGGCTCTC AGGAGCAGGA CACAAGAGAC GGTTATGCCC 1680
AAGCACAGAA CACTCTTGGA AAGCCATCCT TTCCCTTCTG CTGACATTCT GACCCCCTCA 1740
AGGGTTGTCC ATGGGGAACA GGCTTTCTGC ACCCAATTGA CCAAAAAATA ACAGAAGCCT 1800
TCTCCTTAAG AAAGAGAGCA GGCCAGACAC AGTGGCTCAC GCCTATAATC CCAGTGCTTT 1860
GGGAGGCTGA GGTGGGAGAA TTGCTTGAGC CCAGGAGTTC AAGACCAGCC TGGGCAACAC 1920
AATGAGACCT CGTCTCTACA AAAAAACTTA AAAATTAGCC AGGCATGGTC TCAGCTACTC 1980
AGGAAGCTGA GGTGGGAGGA TTGCTTGAGC CCAGGAGGCT GAGGCTGCAG TGAGCCGTGA 2040
TCATGCCACT GCACTCCAAC CTGGACAATA AAGCAAAAGA TCCTGCCTCA AAAAAGAAGA 2100
AAGAGAACAG AGCCCTACAG AGAAGGAAGA AGGCAGGCAC ATTGTCACTT 2150