EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species

TagContent
EnhancerAtlas ID
HS104-00662 
Organism
Homo sapiens 
Tissue/cell
HUVEC 
Coordinate
chr1:19776760-19778300 
TF binding sites/motifs
Number: 2             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
HEY2MA0649.1chr1:19778016-19778026GGCACGTGTC-6.02
Npas2MA0626.1chr1:19778016-19778026GGCACGTGTC+6.02
Number of super-enhancer constituents: 41             
IDCoordinateTissue/cell
SE_00361chr1:19773803-19779686Adipose_Nuclei
SE_01199chr1:19776839-19777408Adrenal_Gland
SE_01199chr1:19777478-19778910Adrenal_Gland
SE_01631chr1:19776831-19781008Aorta
SE_02919chr1:19776836-19777266Bladder
SE_02919chr1:19777430-19778296Bladder
SE_03519chr1:19777019-19778208Brain_Angular_Gyrus
SE_04046chr1:19776718-19778268Brain_Anterior_Caudate
SE_05077chr1:19776737-19784347Brain_Cingulate_Gyrus
SE_05833chr1:19776842-19784637Brain_Hippocampus_Middle
SE_07251chr1:19776697-19779514Brain_Hippocampus_Middle_150
SE_08066chr1:19776762-19779336Brain_Inferior_Temporal_Lobe
SE_09593chr1:19776849-19778375CD14
SE_14589chr1:19776891-19777952CD4_Memory_Primary_7pool
SE_18410chr1:19770426-19778429CD4p_CD25-_Il17-_PMAstim_Th
SE_19269chr1:19776492-19779207CD4p_CD25-_Il17p_PMAstim_Th17
SE_23237chr1:19777327-19778195Colon_Crypt_1
SE_25786chr1:19773798-19779591Duodenum_Smooth_Muscle
SE_26537chr1:19773934-19782356Esophagus
SE_29645chr1:19773867-19779844Fetal_Muscle
SE_31164chr1:19776585-19778418Fetal_Thymus
SE_31447chr1:19776843-19777330Gastric
SE_31447chr1:19777492-19779522Gastric
SE_41031chr1:19776822-19778442Left_Ventricle
SE_42185chr1:19777454-19778394Lung
SE_44300chr1:19776471-19779666NHDF-Ad
SE_45110chr1:19776594-19779780NHLF
SE_45720chr1:19773884-19782578Osteoblasts
SE_46635chr1:19777551-19778408Ovary
SE_47234chr1:19762903-19786782Panc1
SE_48688chr1:19777328-19778427Right_Atrium
SE_50058chr1:19776779-19779520Sigmoid_Colon
SE_51211chr1:19773820-19782386Skeletal_Muscle
SE_52345chr1:19776784-19779874Small_Intestine
SE_53453chr1:19777448-19778185Spleen
SE_54550chr1:19773634-19779785Stomach_Smooth_Muscle
SE_56083chr1:19773877-19779671u87
SE_62519chr1:19761354-19815005Tonsil
SE_65446chr1:19773584-19777190Pancreatic_islets
SE_65446chr1:19777320-19779677Pancreatic_islets
SE_67779chr1:19773877-19779671u87
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr11977715319777959
chr11977704619778046
Enhancer Sequence
GACCTGAAGT GTTTTGGATT TTGAATTTTT TCCAATTTTG AAATACTTGC ATTATACTTA 60
CTGGTTGAGA ATCCCAAATC AGAAAATCCA AAATCCATGT CCCAAAGAAC ATTTCCTTTG 120
AGCCTCATGT CAGTGCTCAC AAAGTTTTGG GTTTTGGAGC ATTCTGGGTT TTAAATTTTC 180
ACATTAGGGA TACTCAGCCT GTAAGAGTGT GTCAGGCACT GTTTTAGGCA TGTAAAATGT 240
GTCAACTCAA TCTTCATAGC ATGCCTGTAA GACAGCTTAT GTTATTAATC CTACTTCATA 300
GATGAGGGGA CTGAGGTAGG GAGAGGTTAA GGAGCTTACC AAATATCACA CAGGTAATAA 360
GTGGCAGAGC TGGAAGCCTG GTTCCAGAGA CCCAGGTGAA TCCCAAAAAA GAGAAGCTGG 420
GCACAAGGCC CCAGGGAAGC AAAAACCTGA AAAACTATCC TTTCACACTT GTGCAGGGTC 480
AGTTGATGTT AGGCTTGTAT TGCAAAATTT ATACTTCTGA AGAAGGATAA AGCAGCAAGA 540
GGGAAAAAGT ATCTAAAATG CAGACACATA TACCACATTT GTTTTGGAAA AGACAAGTCA 600
GGAGCCCACA AAAGGTTATG AAAAACCCCA GTGACACCAC CACCAATGTT TGTCTTTGGA 660
ATAATGGAAA GAGATGTGTA TTACTTGTAA GAATGATCTC TGCTATTACA TGACTCATTC 720
CTGCATGCAA GGACTGCTCT CATCTGGTGC CAAGGAAAGA CTGCTGAATT ATGGAATTGC 780
AAACATTATC ACTGACTGTT ACTCACAACA CTGCAGGGCA AACTGATATG CGCCAAATCA 840
GCCATGTTAA GGGGTTGTTA TTGCACCTCT CCTCAGGACC AGCTGTTGCT ATTTCGCATT 900
AAGACTTTAA CCATATCTTA GTCCAAGAAC TCATCAACCT CAGCAGTTGA GTTGCTTGGA 960
AATGCCCAGG GTCCACACAA GTTCCCCAGG GGAACCCACC ATGGGTCTGG GGACTGGAGT 1020
CATGGGACAA AAAGGGGAAT GGTAGAGGCA GAGAACAGAA ACAGGGAACG GAAACAACAG 1080
ATAAAAGGAA ATCACTGACA CAGATGGCAT GCAAAAGGCC TTTCAGAGTG GAAATGGACA 1140
ATCCCGAAAT TGGCAACATA TGATGTGCTC TTTATTCCTG CTCCCCACCG GCATGTGGTA 1200
GAAGGATGCA GAGGAAAGGA CGGTAATGGG TAAGATAATA TGAATACCAC CCTACAGGCA 1260
CGTGTCATCT AGGAGCCTAC CGAGTGTCCC ACCTTAGTGA TCTGACCCTC AGACAAAACT 1320
GAGAGGGAGA CGCCACCATC CCCACCCTGC AGATGGGAGA CAGAGGCTCT GGGGAGTGGT 1380
CCCCAGAAAC ATGTGGCTAC TCAGAGACAA GGCTAGGACC AGGGGGTGAT CACTTTCCAC 1440
ATGGACAGTG TGGAAATATC AGCCAATAAT GTGTCCTCTA ATCTATTTAT TATGGCCTCC 1500
ACCTCTCTGA TGACTTTAAA GTGCCTCACC CTCAACATAG 1540