EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS197-13989 
Organism
Homo sapiens 
Tissue/cell
ZR75-30 
Coordinate
chr22:41797410-41799080 
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: 3             
ChromosomeStartEnd
chr224179769641798856
chr224179771641798840
chr224179811641798195
Number: 2             
IDChromosomeStartEnd
GH22I041402chr224179718641797462
GH22I041401chr224179749141799127
Enhancer Sequence
GAATGGAACA CCAGCGGCCG GGCGGTGGCT TACGCCTGTA ATCCCAGCAC TTTGGGAGGC 60
CGAGGCAGGT GGATCATGAA GTCAGGAGTT CGAGACCAGC CTGACCAACA TGGAGAAACC 120
CTGTCTACTA AAAATACAAA ATTAGCCAGG CATGGTGGCA CATGCCTGTA ATCCCAGCTA 180
CTCAGGAGGC TGAGGCAGGA GAATCACTTG AACCCAGGAG GCAGAGGTTG CGGTGAGCCG 240
AGATAGTGCC ATTGCACTCC AGCTTGGGCA ACAAGGCGAA ACTCCATCTC AAAAAAAAAA 300
AAACAAAAGC AAAAACGAAC ACCAGCTTCA TAAGACAGTT GTCCCACGAA GACACCTGGA 360
GCAGGGCAAA CACCACTCAG CAGCTGCCAT TATGGTGACA GAGAGGAAGG TACGGACCTA 420
CATGGAGACC ATCACCTCCA GTCCCAGCAG CTGCTGCCCA TCGCGGGTTG TCTACCAGCT 480
GGTGTGGGAT GCAGCCAGGG TCAGACCAGC TGTGTGGTCT TGGACAACTT ATCCATTTCC 540
CTGAGCTGTT TCTCTCTCTG TCCAACAAGG ATGCGCTACA CAGGTCACAT GTGCGTGCCT 600
GACAGCACAT CTCGACCCTT CTCCTTCCCC TCCACCCCAG CTCCTTCAAG GACAAATTCC 660
GAAGCTGGAC ACATGCCCCC TTCCTTTACT GCACCCTATT ACCAGACAGC CCTTCACACA 720
CTGCCCCGTG GCTGTGCCAG GCTGGCCCAG CTGGCAGCTC CTGACGTCAG CAGCTAATCC 780
GGGAAAGCTG CCAGCCAGAG ATAGGGGTGA GCAGCAAAGG AAATCAGAAA CAGGTTTTAA 840
GATGGGTGCC CCAACCCCCC AGCCAGCCCT CAGGGAGCTT TCATCAGCCT CTCACTTAAG 900
CAAATCCTCG CAACCATGCG TCCTGATGCC CGGTCCCCTC AGGATTAAGT AAGTGCTGAG 960
CAGGAGGCTT TTATTTTAAG CTGCAGCTCT GTCATCAGGA GCTAGGCACA CAGCAAGCCA 1020
CTGCCTAGCT GTCCCATAGG TTTCTCCAAA CAGAGTAGTG GGCGTCCACT CAGGTCTGGA 1080
TTTCAGGCTG ACTCCAGGAA GTCCAGACTA CAGGGAGGTA GAGGGGACGG GGCAAAGGTC 1140
AAGGATCAGA GGTAGAGGGG ACAGGACAAG GGCCTCAGTG TGTTGCCTCC AGCTGGCCCT 1200
CCCTCTTAAG GCACAAGGCC CGGTGCACCA TTCCTCACTG TTCTTATGTC TTCCCAGCGT 1260
ACAGCACGCA GGACGGTGCT ATGGTTTGAA TGTCTCCCCA GAATATATGG GTTGGAAACT 1320
TAATCCCTAA TGCAATAGTG TTGGGAGGTG GGTCTTAATG GAAGGTGTTT ACATCGTAAG 1380
GCCTCCACCC TCACGAATGG ATATAAAAGA GCTTGAGGTG GCTGGGTGCG GTGGCTCATG 1440
CCTGTCATCC CAGCACTTTG GGAGGCTAAG GCGGGCAGAT CACCTGAGGT TGGGAGTTCA 1500
AGACCAGCCT GACCAACATG GAGAAAGCCC GTCTCTACTA AAAAGACAAA AATTAGCTGA 1560
GCGTGGTGGC GCACGCCTGT AATCCCAGCT GCTTGGGAGG CTGAGGCAGG AGAATTGCTT 1620
AAACCCGAGA GGCAGAGGTT GTGGTGAGCC GAGATCGGGC CATTGCACTT 1670