EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS099-14846 
Organism
Homo sapiens 
Tissue/cell
HSMMtube 
Coordinate
chr22:41797670-41798720 
TF binding sites/motifs
Number: 6             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
HNF4GMA0484.1chr22:41798536-41798551ACGGGGCAAAGGTCA+6.06
NR2C2MA0504.1chr22:41798536-41798551ACGGGGCAAAGGTCA+6.58
Nr2f6MA0677.1chr22:41798537-41798551CGGGGCAAAGGTCA+6.27
RxraMA0512.2chr22:41798537-41798551CGGGGCAAAGGTCA+6.2
ZNF263MA0528.1chr22:41798028-41798049TTCTCCTTCCCCTCCACCCCA-6.01
ZNF263MA0528.1chr22:41798025-41798046CCCTTCTCCTTCCCCTCCACC-7.53
Number of super-enhancer constituents: 25             
IDCoordinateTissue/cell
SE_01372chr22:41797587-41798792Adrenal_Gland
SE_03173chr22:41797596-41798927Brain_Angular_Gyrus
SE_03911chr22:41796878-41800879Brain_Anterior_Caudate
SE_05807chr22:41796662-41801176Brain_Hippocampus_Middle
SE_06715chr22:41796766-41801019Brain_Hippocampus_Middle_150
SE_07758chr22:41796906-41801025Brain_Inferior_Temporal_Lobe
SE_08854chr22:41797812-41798107Brain_Mid_Frontal_Lobe
SE_08854chr22:41798201-41798804Brain_Mid_Frontal_Lobe
SE_23356chr22:41797656-41798859Colon_Crypt_1
SE_24194chr22:41797716-41798820Colon_Crypt_2
SE_26920chr22:41797675-41798779Esophagus
SE_31944chr22:41797585-41798926Gastric
SE_40631chr22:41797035-41799308Left_Ventricle
SE_41678chr22:41797746-41798755LNCaP
SE_42253chr22:41797639-41799027Lung
SE_46916chr22:41797713-41798745Ovary
SE_47751chr22:41797625-41798846Pancreas
SE_48064chr22:41797599-41799426Psoas_Muscle
SE_48843chr22:41797611-41798932Right_Atrium
SE_49547chr22:41797699-41798891Right_Ventricle
SE_50431chr22:41797601-41798953Sigmoid_Colon
SE_51256chr22:41797373-41799190Skeletal_Muscle
SE_52989chr22:41797572-41798943Small_Intestine
SE_54774chr22:41797122-41800845Stomach_Smooth_Muscle
SE_65292chr22:41796915-41800558Pancreatic_islets
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr224179811641798195
Number: 1             
IDChromosomeStartEnd
GH22I041401chr224179749141799127
Enhancer Sequence
AGCTTGGGCA ACAAGGCGAA ACTCCATCTC AAAAAAAAAA AAACAAAAGC AAAAACGAAC 60
ACCAGCTTCA TAAGACAGTT GTCCCACGAA GACACCTGGA GCAGGGCAAA CACCACTCAG 120
CAGCTGCCAT TATGGTGACA GAGAGGAAGG TACGGACCTA CATGGAGACC ATCACCTCCA 180
GTCCCAGCAG CTGCTGCCCA TCGCGGGTTG TCTACCAGCT GGTGTGGGAT GCAGCCAGGG 240
TCAGACCAGC TGTGTGGTCT TGGACAACTT ATCCATTTCC CTGAGCTGTT TCTCTCTCTG 300
TCCAACAAGG ATGCGCTACA CAGGTCACAT GTGCGTGCCT GACAGCACAT CTCGACCCTT 360
CTCCTTCCCC TCCACCCCAG CTCCTTCAAG GACAAATTCC GAAGCTGGAC ACATGCCCCC 420
TTCCTTTACT GCACCCTATT ACCAGACAGC CCTTCACACA CTGCCCCGTG GCTGTGCCAG 480
GCTGGCCCAG CTGGCAGCTC CTGACGTCAG CAGCTAATCC GGGAAAGCTG CCAGCCAGAG 540
ATAGGGGTGA GCAGCAAAGG AAATCAGAAA CAGGTTTTAA GATGGGTGCC CCAACCCCCC 600
AGCCAGCCCT CAGGGAGCTT TCATCAGCCT CTCACTTAAG CAAATCCTCG CAACCATGCG 660
TCCTGATGCC CGGTCCCCTC AGGATTAAGT AAGTGCTGAG CAGGAGGCTT TTATTTTAAG 720
CTGCAGCTCT GTCATCAGGA GCTAGGCACA CAGCAAGCCA CTGCCTAGCT GTCCCATAGG 780
TTTCTCCAAA CAGAGTAGTG GGCGTCCACT CAGGTCTGGA TTTCAGGCTG ACTCCAGGAA 840
GTCCAGACTA CAGGGAGGTA GAGGGGACGG GGCAAAGGTC AAGGATCAGA GGTAGAGGGG 900
ACAGGACAAG GGCCTCAGTG TGTTGCCTCC AGCTGGCCCT CCCTCTTAAG GCACAAGGCC 960
CGGTGCACCA TTCCTCACTG TTCTTATGTC TTCCCAGCGT ACAGCACGCA GGACGGTGCT 1020
ATGGTTTGAA TGTCTCCCCA GAATATATGG 1050